Structure, regulation, and mechanisms of nonmuscle myosin-2

Members of the myosin superfamily of molecular motors are large mechanochemical ATPases that are implicated in an ever-expanding array of cellular functions. This review focuses on mammalian nonmuscle myosin-2 (NM2) paralogs, ubiquitous members of the myosin-2 family of filament-forming motors. Through the conversion of chemical energy into mechanical work, NM2 paralogs remodel and shape cells and tissues. This process is tightly controlled in time and space by numerous synergetic regulation mechanisms to meet cellular demands. We review how recent advances in structural biology together with elegant biophysical and cell biological approaches have contributed to our understanding of the shared and unique mechanisms of NM2 paralogs as they relate to their kinetics, regulation, assembly, and cellular function.


Introduction
Members of the myosin superfamily are ubiquitous actinbased molecular motors in eukaryotes.In humans, the protein products of the 39 myosin genes are grouped into 12 distinct classes.The largest class of myosins is referred to as class-2 and consists of 10 sarcomeric myosin-2 paralogs, one smooth muscle myosin-2 paralog, and three nonmuscle myosin-2 (NM2) paralogs at the protein level [1,2].The three NM2s (NM2A, NM2B, NM2C) are expressed from three genes (MYH9, MYH10, MYH14) in a tissue-specific and developmentally-dependent manner [3,4].NM2 paralogs are phylogenetically more closely related to smooth muscle myosin-2 than to sarcomeric myosin-2s [5].NM2 genes are broadly expressed and their gene products have been implicated in countless fundamental processes with particular relevance to cell adhesion, division, and migration [3,6].NM2 paralogs have diverse and specialized roles in cells, share highly conserved structural features, and generate mechanical force by pulling on antiparallel actin filaments.Thereby, they directly influence actin organization,

Cellular function and disease
The understanding of the emergent and multifaceted roles of NM2 paralogs in essential cellular processes including cell division, migration, differentiation, and adhesion was greatly facilitated through the generation of various animal models in conjunction with elegant cell biological studies.Mouse models revealed specific as well as redundant functions for NM2 paralogs during development.The comparison of NM2 expression patterns in the developing mouse embryo shows a broad tissue distribution at E11.5 with paralog-specific enrichments in organs, tissues, and cell types [4].For example, NM2A is enriched in the vasculature, NM2B in neurons, and NM2C in the pituitary gland in the brain [4].NM2A and NM2C are enriched in epithelial cells whereas NM2B is enriched in serosal cells of the intestine at E16.5 [4,5].Ablation of NM2A or NM2B in mice is lethal at E6.5 and E14.5, respectively [4,14,24,25].Mice ablated for NM2C show no obvious defects and survive to adulthood [16].Ablation of NM2A in mice results in defects in the development of the placenta that cannot be rescued by the expression of NM2B from the Myh9 locus [4,11].Animal models also showed that NM2B is essential for the development of the heart.Ablation of NM2B reduces the proliferation and causes the misalignment of cardiac myocytes [4,16,24,26].At the cellular level, NM2B, but not NM2C, has been shown to play key roles in cell division in normal cells.Small interfering RNA knockdown of NM2B results in multinucleated cells in vitro and knockout of NM2B in a mouse model results in a ~ 70% decrease in the number and in an increase in binucleation of cardiac myocytes from 1 to 23% compared to control myocytes by E12.5 [16,26,27].The detailed mechanisms of NM2 paralogs play in diverse cellular processes have been reviewed in detail elsewhere [3,[28][29][30].
Mutations in genes encoding NM2 paralogs have been associated with human diseases.Heterozygous mutations in MYH9 cause MYH9-related disorders (MYH9-RD) that are characterized by macrothrombocytopenia with or without granulocyte inclusions, nephritis, or sensorineural hearing loss [31].Further, mutations in MYH9 have been associated with autosomal dominant deafness (DFNA17) [32].Interestingly, mice harboring MYH9-RD point mutations exhibit anomalies associated with the disease but also cause male infertility, which is unreported in humans [19,33].Mutations in MYH14 have been associated with peripheral neuropathy, myopathy, hoarseness, and hearing loss (PNMHH) in addition to autosomal dominant nonsyndromic deafness (DFNA4A) [31].More recently, a link between heterozygous mutations in MYH10 and neurodevelopmental disorders as well as congenital abnormalities in most organ systems has been proposed [34,35].

Domain architecture
NM2s have a modular domain organization and share common structural characteristics at the protein level [36,37].The myosin heavy chain contains an amino-terminal motor domain, a central neck domain, and a carboxy-terminal tail domain (Fig. 1a).NM2 paralogs share a high overall sequence identity (~ 65-78%) with ~ 77-86% sequence identity in the motor domain and ~ 57-73% in the tail (Fig. 1b, c).The motor is a globular ~ 15 nm domain that represents the minimal enzymatically active unit (Fig. 2a).The motor domain contains a nucleotide binding pocket and a binding region for filamentous actin (Fig. 2a, b) [38].The neck domain contains two IQ motifs that are binding sites for the essential light chain (ELC) and the regulatory light chain (RLC) [39].The neck domain together with the bound light chains functions as a lever arm during the myosin mechanoenzymatic cycle.Myosin light chains are small EF-hand proteins that confer stabilizing and regulatory functions and possibly directly modulate the enzymatic activity of myosin-2 paralogs [40,41].To this date, it remains largely unclear which ELC and RLC isoforms are bound to the NM2 heavy chain in cells [40].
The myosin tail provides the structural framework for the self-assembly of two myosin heavy chains and the assembly of NM2 paralogs into filaments [36].The tail folds into an extended ~ 160 nm long α-helical structure and ends in a short non-helical tailpiece (NHT).The α-helical tail forms a coiled-coil through hydrophobic interactions that direct the self-assembly of two myosin heavy chains and the bound light chains into an elongated hexameric complex of ~ 525 kDa that is referred to as the monomer.The monomer is the basic building block of NM2 and can further assemble into filaments as well as higher-order filament stacks, as discussed below [42][43][44][45][46][47].
Mutations have been reported for all human NM2 heavy chain genes and linked to a range of debilitating diseases including blood and kidney disorders, hearing loss, infertility, neurodevelopmental disorders, and cancer [4,19,48,49].Although the functional consequences of most mutations have not been explored at the protein level, the trend is that mutations in the motor domain decrease enzyme activity while mutations in the tail may alter the assembly properties of NM2 paralogs [50,51].Notably, mutations have not been reported in the genes encoding for the NM2 ELC and RLC, unlike in sarcomeric light chain genes where mutations have been linked to different types of cardiac and skeletal myopathies [52].

Mechanoenzymatic cycle
NM2s convert chemical energy into mechanical force by coupling structural changes in the myosin motor domain to a conserved enzyme cycle (Fig. 2c) [53,54].In this mechanoenzymatic cycle, ATP is the substrate, and actin serves as a nucleotide exchange factor for myosin.Per one molecule of ATP hydrolyzed, actin is displaced one discrete distance past myosin.Four major structural states can be distinguished as myosin transitions through its mechanoenzymatic cycle as revealed by crystallographic, negative staining electron microscopy, cryo-electron microscopy (cryo-EM), and kinetic studies (Fig. 2c).In the nucleotidefree rigor state, NM2 tightly binds to actin.The rigor state has higher affinity for actin than the myosin •ATP state [55][56][57].Therefore, ATP binding to the actin-bound myosin motor domain causes the dissociation of myosin from actin.Myosin hydrolyzes ATP to ADP and P i while it undergoes a conformational change, the recovery stroke, that puts the motor in a primed conformation [58].The ADP•P i state is a stable intermediate with weak actin affinity.Myosin rebinds actin and a conformational change in myosin results in the relative ~ 7 nm displacement of both proteins [59].The powerstroke is associated with the release of P i but it is still controversial whether both events occur simultaneously or not [60,61].ADP is released at the end of the powerstroke and concludes the cycle.
Kinetic studies on single-headed myosin fragments showed that NM2 paralogs and their isoforms have unique kinetic profiles associated with their individual mechanoenzymatic cycles.NM2s are classified as strain sensors and are amongst the slowest myosins that have been kinetically characterized in vitro [55][56][57][62][63][64][65][66].A key feature of the mechanoenzymatic cycle of NM2 paralogs is a low basal ATPase activity that is marginally activated by actin under steady-state conditions, resulting in a poor catalytic efficiency (k cat /K app ) compared to other myosin-2s [55][56][57]67].A kinetic signature of NM2 paralogs is that actin binding does not significantly accelerate the release of ADP from the nucleotide binding pocket [55][56][57].This contributes to small kinetic (k -AD /k -D ) and weak thermodynamic (K AD /K D ) coupling ratios.Therefore, ADP binding does not significantly change the actin affinity of NM2s and vice versa [68].The low actin-activated ADP release is thought to contribute to a slow in vitro sliding velocity [55,59,65].Together, these kinetic signatures result in a duty ratio that is higher compared to that of other myosin-2 paralogs, meaning that NM2s spend a larger amount of time during their enzyme cycle strongly bound to actin [63].
NM2s have a well-defined kinetic behavior in the monomeric form but a very complex collective behavior once they are assembled into filaments.Strikingly, the number of monomers in an NM2 filament is reciprocal to the duty ratio.This ensures that a collective duty ratio > 0.8, which is required for robust motion, is achieved and allows NM2 filaments to move processively and to generate force and Fig. 1 Heavy chain domain organization and structural conservation of human NM2 paralogs a. Heavy chain domain organization of a generic human NM2 paralog featuring an N-terminal motor domain (pink), a central neck domain that contains two IQ motifs (grey), and a C-terminal tail domain (green).Schematic not drawn to scale.b, Percent identity matrix summarizes the degree of identity between the heavy chains of human NM2 paralogs (left), the motor domain (middle) and the tail domain (right).c, Consurf analysis [197] shows the conservation of amino acid positions in the structure of the NM2C motor domain (PDB ID: 5I4E).Views are rotated by 180º

Structure
A significant advance in our understanding of the molecular mechanisms of myosin motors occurred when the structure of a single-headed myosin-2 fragment was published ~ 30 years ago [38].Since then, high-resolution crystal structures of human NM2B (PDB ID: 4PD3, nucleotide-free state) and human NM2C (PDB ID: 5I4E, pre-powerstroke state) motor domains in different nucleotide states as well as a cryo-EM structure of the human NM2C (PDB ID: 5JLH, rigor state) motor domain bound to actin have been solved [61,77,78].Though the basic features of the motor domain are common to all myosins-2 structures solved to date, including those from model organisms, they are valuable resources to understand the allosteric nature of myosin motor function that lead to kinetic fingerprints and paralog-and isoformspecific cellular activity profiles [38,60].movement in cells [59,65,69,70].The lower duty ratio of NM2A compared to NM2B likely contributes to the ability to generate faster contractions in cells while the higher duty ratio of NM2B suggests that it can bear more load [8].
An important tool that has significantly contributed to our understanding of NM2 function is the popular myosin-2 inhibitor blebbistatin and its derivatives [71,72].Blebbistatin is an uncompetitive inhibitor that almost completely inhibits the ATPase activity of all NM2 paralogs with low micromolar affinity (IC 50 ~ 0.5-5 µM) by trapping myosin in the weak actin binding ADP•P i state, thus slowing down phosphate release and entry into the strong actin binding state [73][74][75].Recently, it has been reported that the small molecular inhibitor of formin FH2 domains, SMIFH2, inhibits myosin motors including NM2A with an IC 50 of ~ 50 µM in vitro and NM2A-dependent cellular functions at lower concentrations in cells [76].The observed cross-reactivity of SMIFH2 suggests that this inhibitor should be used with extreme caution and rigorous controls when studying either formin or NM2, as it may introduce potential confounding effects.between the U50 and the L50 [83].The high-resolution cryo-EM structure of NM2C in the strong actin binding apo state revealed that the interface between both proteins is mainly stabilized by hydrophobic interactions [61].Actin binding is initiated by hydrophobic interactions with loop-2 that connects the L50 and the U50 of the motor domain and plays a central role during the initial formation of the actomyosin interface [61].This interaction is thought to promote the closure of the cleft that is required for the strong binding of myosin to actin.The helix-loop-helix motif (HLH) in the L50 contributes to a strong actin binding interface through hydrophobic and electrostatic interactions with actin [61].The CM-loop in the U50 interacts with actin through hydrophobic and weak electrostatic interactions.Loop-3 of the L50 engages in weak charged interactions with actin [61].The structure also revealed that in NM2C, the activation loop that has been suggested to directly bind to actin and activate the enzyme function of some class-2 myosins, is part of the actomyosin interface in the apo state [61,85].

Alternative splicing in the motor domain
Kinetic and functional signatures of NM2s are fine-tuned by alternative splicing in flexible surface loops-1 and − 2 that extend the core of the myosin motor domain.This generates a large number of NM2 isoforms from a small number of genes [5,86,87].NM2 isoforms have either an insert in loop-1 (A1, B1, C1), an insert in loop-2 (A2, B2, C2) or both inserts (B1B2, C1C2) [5,86,87].Loop-1 is located in the U50 and is a key regulator of ADP kinetics.Compared to isoforms with uninserted loops (A0, B0, C0), an extended loop-1 allosterically accelerates the ADP release and therefore the in vitro sliding velocity of NM2s, similar to what has been observed with smooth muscle myosin-2 [51,55,88].NM2 isoforms with extended loops-2 have a higher catalytic activity (k cat ) under steady-state conditions and increased actin binding rate constants in the presence and absence of ADP [55].Alternatively spliced loops-1 and − 2 not only fine-tune NM2 kinetics but also affect the regulation of NM2 isoforms in vitro.For example, the NM2C isoform with the C2 insert is constitutively active and does not require RLC phosphorylation for maximum actin-activated steady-state ATPase activity and in vitro motility [89].This is in striking contrast to the NM2B isoform with the B2 insert that lacks actin-activated steady-state ATPase activity and in vitro motility after RLC phosphorylation [90].The structural origin of these differences remains unclear since the B2 insert does not interfere with the formation of the autoinhibited (10S) state and/or filament formation, as discussed below, suggesting an alternate mode of regulation that directly affects kinetics.Notably, subtle changes in the kinetic properties are indispensable for the specialized

Motor domain
The highly conserved mechanochemical core of the NM2 motor domain is composed of a seven-stranded β-sheet flanked by α-helices on each side, reminiscent of that found in other myosins and evolutionarily related G proteins and kinesins (Fig. 2a) [38,79,80].This arrangement generates four functional and allosteric subdomains in the myosin motor domain: The N-terminal subdomain (Nter), the upper 50 kDa subdomain (U50), the lower 50 kDa subdomain (L50), and the converter (Fig. 2a) [60,81].The U50 and the L50 are separated by a large cleft in the absence of actin [38].
The nucleotide binding pocket is the catalytic core of NM2 (Fig. 2b).It is formed by structural elements of the U50 and features three conserved nucleotide binding motifs: P-loop (GESGAKT), switch-1 (NXNSSRGF), and switch-2 (DIXGFE) [79].Nucleotide binding to the motor domain is sensed by the phosphate-binding P-loop and causes the movement of switches-1 and − 2 during the myosin ATPase cycle.Switch-1 and − 2 form a characteristic salt bridge in the closed conformation that is critical for the hydrolysis of ATP [38,[82][83][84].The closed conformation of the nucleotide binding pocket is linked to the converter and the lever arm in the 'up' position (ATP, ADP•P i ) while an open nucleotide binding pocket is associated with the converter and the lever arm in the 'down' position (apo, ADP).The different converter and lever arm conformations are allosterically communicated with the nucleotide state of the nucleotide binding pocket through conformational changes in the relay helix.The Nter/converter/lever arm interface is critical for NM2 kinetic signatures and its distortion is thought to contribute to the reported load-sensitivity of NM2 paralogs [77].
The ~ 10 Å long neck domain distal to the myosin motor domain functions as a lever arm.It amplifies small-scale movements in the motor domain to a large scale, 60-70˚ movement (Fig. 2c), thereby forming the structural basis for the powerstroke of NM2s [79].The nucleotide binding pocket is flanked by the JK-loop.A reduction in the length of this loop in NM2C disrupts key interactions with switch-1 and the nucleotide and renders the active site more assessable compared to other myosin-2 paralogs, possibly contributing to their low catalytic efficiency [77].
The actin binding region is a large and dynamic interface that is formed by structural elements of the U50 and the L50.It is located > 40 Å from the nucleotide binding pocket.Changes in the actin binding interface in response to nucleotide binding, hydrolysis, and product release are reflected in differential affinities of myosin for actin [60].The movement of switch-1 in response to nucleotide binding and release is linked to the opening/closing of the cleft in the ACD between the three NM2 paralogs allows them to assemble into either homotypic filaments but also into heterotypic and mixed filaments [106].While homotypic filaments are composed of one NM2 paralog, heterotypic filaments are composed of two NM2 paralogs, whereas mixed filaments are composed of a NM2 paralog and a small number of enzymatically inactive myosin-18A molecules [42,43,46].The NHT is absent in sarcomeric myosins, suggesting that its presence in NM2s and smooth muscle myosin-2 is connected with the ability of the latter myosins to dynamically assemble and disassemble to meet contractile cellular demands [104].The exact contribution of the NHT on the in vitro assembly of NM2s has not been systematically addressed with full-length proteins so far and deletion studies with NM2 tail fragments, which tend to form non-physiological paracrystals opposed to discrete bipolar filaments, have resulted in conflicting results [104,108,109].The presence of phosphorylation sites within the coiled-coil tail domain and the NHT further suggest regulatory functions, as discussed below [110].In cells, filament assembly, and disassembly are likely modulated by the synergistic effect of the NHT and tail phosphorylation [111].While the aforementioned domains and structural motifs are conserved across mammalian NM2s, the NM2B heavy chain additionally features a ~ 7 amino acid long regulatory motif (RM) between the coiled-coil tail and the NHT [112].The RM contains five serines out of which several are phosphorylated in cells.Phosphorylation of S1935 has been identified as the primary regulatory site that controls NM2B assembly and dynamics during front-back polarization in migrating cells [112].

Filaments and higher-order organization
NM2 exists in two global states: autoinhibited (10S) and filamentous.In the presence of ATP and the absence of phosphorylation of S19 in the RLC (S19 RLC ), NM2 assumes a compact, autoinhibited conformation known as 10S in reference to its sedimentation coefficient [113,114].Myosin in this conformation is thought to be diffusible and assemblyincompetent [10].In the 10S conformation, the two motor domains, the blocked head (BH) and the free head (FH), asymmetrically dock against each other in a conformation known as the interacting heads motif (IHM) in analogy to the structure that likely contributes to the super-relaxed state of cardiac muscle myosin-2 [115,116].The tail folds in three places, loops around the IHM, and folds back on itself [117].This complex folding of the monomer inhibits the release of P i ~ 100-fold and traps the enzymatically inactive myosin in a weak actin-binding ADP•P i state (K D > 100 µM) [118].Phosphorylation of S19 RLC relieves the 10S state and promotes filament formation, as discussed below in vivo functions of NM2 isoforms as they have individual expression patterns, intracellular localizations, and binding partners [11,[91][92][93].For example, the B1 isoform is expressed during embryonic development whereas the B2 isoform is only expressed after birth [91].The ablation of the B1 isoform results in the abnormal migration of facial neurons and the development of hydrocephalus in a mouse model [91].In contrast, the ablation of the B2 isoform results in the abnormal maturation of cerebellar Purkinje cells and impaired motor coordination [91].The observation that homologous mutations have distinct effects in different NM2 paralogs and isoforms suggests individual allosteric regulation mechanisms [51].Alternate splicing in surface loops therefore creates kinetic, regulatory, and functional diversity in NM2 paralogs.

Neck domain and tail domain
The neck domain is a short ~ 10 Å long α-helical structure that features two IQ motifs [94].The first consensus IQ motif ([I, L,V]QXXXRXXXX[R, K]) is the binding site for the ELC and the second divergent IQ motif is the binding site for the RLC [38,40].A sharp bend, the hook, features a conserved WQWW motif that interacts with a portion of the RLC and connects the neck to the tail domain [38].An invariant proline marks the neck/tail junction and helps in orienting the myosin motor domains to engage with actin.
The tail domain forms a long α-helix and ends in an NHT.The tail domains of two myosin heavy chains dimerize into an extended left-handed coiled-coil.The coiledcoil is formed from a series of consensus heptad repeats (a-b-c-d-e-f-g) n in which positions a and d are commonly occupied by hydrophobic amino acids [95,96].A 28 amino acid repeat pattern of four heptads along the length of the tail produces an alternating pattern of positive and negative charged zones that have been implicated in the parallel and antiparallel alignment of adjacent tail domains in an NM2 filament [97][98][99].The periodic 28 amino acid repeat is interrupted at 3 places by the insertion of skip residues that introduce regions of flexibility in the coiled-coil and lead to local structural changes and discontinuities [100,101].The exact role of the individual skip residues in NM2s has yet to be explored but they are likely to keep the alternating pattern of positive and negative charged zones in phase to promote proper filament assembly, as it has been shown for muscle myosin-2s [100,102].
The end of the tail domain contains two ~ 35-39 amino acid long assembly competence domains (ACD) and ends in a ~ 35-43 amino acid long NHT [103][104][105].The two conserved ACDs, ACD1 and ACD2, of two NM2 monomers form an antiparallel homodimer through electrostatic interactions [103,106,107].The high sequence conservation axial staggering of their coiled-coil tail domains via electrostatic interactions, as described above [98,103].
Self-assembly and force generation are tightly coupled and essential for the biological function of NM2 paralogs.The structural and molecular mechanisms that underlie the processes of filament assembly and disassembly however are less well understood.Negative staining electron microscopy and computational studies suggest that NM2s assemble from 10S, antiparallel 10S dimers, and possibly tetramers and higher order oligomer intermediates that unfold and associate with an existing filament through rolling and zipping motions (Fig. 3) [126,127].However, quantitative analytical ultracentrifugation and interferometric scattering measurements showed that the 10S state is predominant under physiological conditions and only a very small portion of myosin molecules may form transient higher-order oligomers [23,113], indicating that our understanding of the processes of filament assembly as well as disassembly is still incomplete.
In a filament, ~ 29 (NM2A) or ~ 30 (NM2B) monomers work cooperatively to produce force and motion in the actin cytoskeleton.NM2C filaments are thinner and contain ~ 14 monomers [117].NM2 filaments have a contour length of ~ 300 nm, a width between ~ 7.9-11.5 nm, and bare zones between ~ 166-219 nm [117,128,129].Due to the significantly shorter length and the reduced number of heavy chains compared to striated muscle myosin-2 filaments, [114,119,120].The dynamic shape changes from the 10S to the filamentous state and vice versa are important to drive biological processes associated with the mechanical properties of cells [10,121,122].The molecular mechanism and structural changes that drive the activation mechanism have recently been revealed by high-resolution cryo-EM of the closely related smooth muscle myosin-2 [123][124][125].The structure showed that in 10S, the RLC BH and RLC FH adopt unique conformations that bury the phosphorylatable S19 of the RLC FH [123].The phosphorylatable S19 RLC on the RLC FH contacts the folded tail and is accessible for kinases [123].This suggests that 10S relief by phosphorylation is a sequential process that involves the phosphorylation of S19 RLC on the RLC FH , a series of conformational changes that weaken the RLC BH :RLC FH interface and finally make S19 on the RLC BH available for phosphorylation by RLC kinases [123].In addition, the pathway likely involves changes in the interactions between the RLC and the ELC as well as the ELC and the motor domain [123].Importantly, S19 RLC phosphorylation does not directly activate the enzymatic activity of NM2 but rather prevents myosin from adopting the IHM which shuts down the activity.Evidence in support of this included the observation that single-headed NM2 fragments from higher eukaryotes are constitutively active and not regulated by phosphorylation [55-57, 62, 69].Upon RLC phosphorylation, NM2 monomers assemble into bipolar, highly organized filaments through a well-defined Dashed lines indicate putative regulation mechanisms.Force: force dependent maturation of heterotypic filaments NM2B acts as a break to limit the collective activity of filaments containing NM2A [134].Further, it has been reported that the actin mesh size limits the degree of penetration of myosin minifilaments into the cell cortex by steric effects, suggesting that the degree of penetration determines cortical tension [9].Notably, NM2A and NM2B localize to nearly identical structures such as cell-cell junctions and large contractile bundles while NM2C is absent from stress fibers and larger contractile bundles in epithelial cells [137,138].It was also shown that NM2C localizes independently from NM2A in brush border microvilli [139].
NM2 filaments are dynamic assemblies that split, concatenate, and form higher-order stacks in cells [44,122,140].In stacks, dozens of parallel NM2 filaments stack on one another and form a sarcomere-like registry perpendicular to actin bundles [44,128,141].Stacks have been observed in various cell types and appear to be involved in the positioning and movement of actin bundles and the regulation of contractile actomyosin structures for example in interphase and dividing cells [44,45,122,140,142].In stress fibers, myosin-18B localizes at the ends of NM2 stacks and contributes to the assembly of large stacks that are critical for the generation of contractile actomyosin bundles [45].High-resolution imaging further revealed that stacks are associated with the minus end of the actin filament [44].Stacks can span several actin bundles that are separated by ~ 100 nm, suggesting long-range interactions.Stacks are formed by the parallel fusion of adjacent individual filaments and small stacks into large stacks and disassemble by splitting [44,45,122,140,143].Stack formation is a slow process that takes tens of minutes and depends on NM2 motor activity and the balanced activities of actin binding (ABP), crosslinking, and regulatory proteins [44,45,122].The ABPs α-actinin-4 and cofilin1 in addition to the actin assembly factor formin-like 3 and unconventional myosin-18B are positive regulators of NM2 stack formation whereas tropomyosin isoforms 1-4 are negative regulators (Fig. 3) [44,45,47,144].Recent studies further suggested that in addition to NM2 filament assembly and disassembly, cells can also regulate the degree of order in their longrange organization which is important to match their force requirement [144].
NM2 stacks have also been observed at cell-cell junctions [142,145].In contrast to stacks observed in fibroblasts, NM2 is organized in extensive, micrometer-scale arrays of stacks in adherens junctions of epithelial cells [145].Extensive arrays of stacks that span ~ 4-6 μm are formed in locations of more loosely organized actin networks in younger junctions.During junction maturation, the span of these arrays narrows to ~ 200-300 nm without a significant change in the spacing between individual stacks [145].Stack narrowing likely contributes to the bundling NM2 filaments are also referred to as minifilaments.A mature minifilament composed of 30 monomers has five crowns of three monomers that are projecting out on each side based on in silico studies [126].The RLC-phosphorylated motor domains are splayed away from the filament backbone, allowing them to survey for actin binding sites within tens of nanometers [117,126].Negative staining electron microscopy showed that NM2 filaments can bind single or multiple actin filaments either via one or both ends of the myosin filament [117,130].This likely determines the interaction and force generation of NM2s on actin structures with different nanoarchitectures in the cell that can give rise to contractile and potentially extensile forces [131].Interestingly, a recent super-resolution microscopy study showed that in the cell cortex of interphase cells, NM2 minifilaments do not fully overlap with actin.A reduced actin-myosin overlap has been correlated with reduced cortical tension, leading to the speculation that minifilaments may only be bound to actin filaments with one end in cells, as it has been observed in vitro [9,117,130].
NM2 paralogs can not only assemble into homotypic filaments but also into heterotypic and mixed filaments (Fig. 3) [42,43,46].The co-assembly of myosins at different ratios gives rise to filaments with a broad range of kinetic and dynamic properties that are needed to perform specialized functions during processes including cell migration and division [132,133].For example, the co-assembly of NM2A into an NM2B filament is expected to decrease the collective duty ratio and accelerate filament dynamics and biochemical properties.Likewise, in vitro experiments showed that the incorporation of NM2B into a non-processive NM2A filament allows the heterotypic filament to move processively on actin filaments [65].This also suggests that the slower myosin determines the speed of movement of the heterotypic filament [65].In silico studies revealed that homotypic filaments of NM2A and heterotypic NM2A/ NM2B filaments are stable, whereas NM2B and NM2C filaments appear less stable [126].Mathematical modeling further proposed that the ATPase activity of NM2 paralogs directly translates into the observed differences in minifilament stability [134].
A mechanistic model suggests that if NM2 paralogs co-assemble with equal probability and proportionally to their cellular availability, a gradient distribution of NM2A, mixed NM2A/B, NM2B/A, and NM2B would emerge from the front to the rear in migrating cells [132].This spatial distribution of minifilaments has been experimentally observed in cells [121,132,[134][135][136].In knock-out cell lines, it was shown that NM2A and NM2B play a distinct role during filament formation.Quantitative imaging and mathematical modeling suggest that NM2A forms initiating filaments to which NM2B incorporates.In those heterotypic filaments, S19 RLC -phosphorylated myosin differentially regulates adhesion and polarity in migrating cells and the assembly and stability of NM2 paralogs [149,150].At the mitotic cortex, it was shown that MLCK and ROCK preferentially create short-lived S19 RLC -phosphorylated and long-lived T18 RLC /S19 RLC -phosphorylated NM2 species, respectively, suggesting a graded effect on NM2 turnover [151].While phosphorylation of residues S1, S2, and T9 by protein kinase C (PKC) has been reported to increase the K app of myosin light chain kinase for the RLC in vitro, the physiological significance of this inhibitory phosphorylation remains to be established [152][153][154].MLCP dephosphorylates serine and threonine residues on the RLC [155,156].Phosphatase activity is inhibited through phosphorylation of its regulatory myosin binding subunit (MYPT1) by ROCK and other kinases [155][156][157][158]. Therefore, the dual action of some kinases to promote RLC phosphorylation determines the extent, duration, and location of actomyosin contractility which is counterbalanced by MLCP.It is of note that a recent super-resolution microscopy study reported that the level of S19 RLC phosphorylation scales with the expression level of MYH9 and to a lower degree with the expression of MYH10 while the expression of MYH14 does not scale with S19 RLC phosphorylation [134].Together with the observation that the loss of MYH9 expression negatively affects the assembly of NM2B, this suggests that the local activation of NM2A through S19 RLC phosphorylation and the subsequent assembly into filaments likely facilitates the co-assembly of NM2B into existing NM2A filaments [134].
In addition to the phosphorylation of serine and threonine residues, tyrosine phosphorylation of the RLC has been investigated [147,159].Phosphorylation of Y155 by epidermal growth factor receptor interferes with the interaction between the RLC and the NM2 heavy chain and filament assembly [147].Y155 phosphorylation is spatially restricted to the lamellipodium and contributes to the compartmentalization of NM2 assembly in cells [147].

Heavy chain phosphorylation
While light chain phosphorylation is a paralog-redundant mechanism of NM2 regulation, myosin heavy chain phosphorylation is predominantly paralog-specific (Fig. 3).Unlike in lower eukaryotic myosin-2s, designated myosin heavy chain kinases have not been identified in mammalian cells where several common kinases including PKC isoforms, casein kinase 2 (CK2), and p21-activated kinase 1 (PAK1) have been shown to phosphorylate serine and threonine residues in the NM2 tail [160][161][162][163]. Tyrosine phosphorylation in the myosin heavy chain has also been reported but the physiological consequences remain to be explored [164,165].Sites and consequences of of actin filaments and the formation of sarcomere-like actomyosin arrays at mature junctions, suggesting that the selforganization of NM2 contributes to the organization of the actin cytoskeleton [145].
Biochemical studies on stacks significantly lagged behind cellular studies.Hence, the molecular mechanisms and structural basis of stacks are largely unexplored.Negative staining electron microscopy suggested that stacks are formed by lateral and serial interactions of single NM2 filaments [65,117].Since the merging of individual filaments into stacks and the splitting of stacks has been observed in a 2-dimensional in vitro motility assay, it has been proposed that the electrostatic forces that hold stacks together are of similar magnitude as the force exerted by a myosin filament on actin [65].Interestingly, disease-causing mutations in both the NM2 motor and the tail domain have been shown to alter stack formation in cells without affecting the capability of myosin molecules to assemble into filaments in vitro per se [19,50].However, filament parameters including width, length, number of NM2 molecules per filament, and the length of the bare zone show mutant-specific changes, suggesting a complex effect of mutations on filament and stack dimensions [50].

Regulation mechanisms
NM2 activity is tightly controlled at multiple levels by synergistic regulatory mechanisms that work in concert to ensure bona fide cellular function.Factors that influence NM2 function in cells include for example the complex intracellular environment, compartmentalization, proteinprotein interactions, posttranslational modifications, and mechanical forces.

Regulatory light chain phosphorylation
The reversible phosphorylation of the RLC by opposing activities of numerous kinases and myosin light chain phosphatase (MLCP) is tightly controlled by many signaling pathways to regulate NM2 dynamics and assembly (Fig. 3) [119,[146][147][148]. Super-resolution microscopy studies revealed that the two major RLC kinases -myosin light chain kinase (MLCK) and Rho-associated protein kinase (ROCK) -compete for a limiting pool of NM2 monomers for the spatiotemporal control of actomyosin contractility in cells [122].Biochemical studies revealed that phosphorylation of the S19 RLC promotes autoinhibition relief, filament formation, and therefore the spatial and temporal control of contractility and force generation, as reviewed in greater detail elsewhere [3,6,30,48].Phosphorylation of the RLC on T18 (T18 RLC ) -in addition to S19 -has a small effect on the enzyme activity of NM2 but T18 RLC / actin-NM2 interface [170].Other posttranslational modifications such as ADP-ribosylation of α-actin on T148 by the bacterial toxin TccC3 have no significant effect on the steady-state kinetics of NM2B [171].In cells, the majority of actin filaments are associated with tropomyosins as well as other ABPs.Decoration of actin with tropomyosin isoforms showed varying effects on gliding speeds and ATPase activities of NM2 paralogs in vitro, suggesting that the paralog itself is the major determinant of the observed effects on the actin-myosin interaction [172][173][174][175]. Further, N-terminal acetylation of tropomyosin impacts the actinactivated ATPase activity and in vitro motility of NM2A in an isoform-specific manner [175].
Modulation of the basic actin-myosin interaction by alternatively spliced surface loops in NM2, several posttranslational modifications of actin isoforms and ABPs that diversify actin cytoskeletal structure, generates countless actin-ABP-NM2 combinations that may modulate cytoskeletal function in time and space.This suggests that the local composition of the actin cytoskeleton fine-tunes the enzymatic output of NM2 motors which may also contribute to myosin sorting and the generation of different actin landscapes in cells.
The myosin tail domain is also a binding site for interacting partners that negatively affect NM2 filament assembly and/or disassembly and therefore may change the equilibrium between the homotypic and the heterotypic filament pool and paralog sorting [132,161].Negative regulators of NM2A filament assembly include structurally diverse proteins including myosin binding protein H, lethal giant larvae, and members of the S100 protein family [176][177][178].The latter selectively disassemble NM2A filaments and/or remove NM2A from heterotypic filaments and have only very little effect on NM2B, where tail phosphorylation seems to be the predominant regulator of filament assembly and disassembly [161,178,179].The selective removal of RLC-phosphorylated NM2A from filaments through S100A family proteins would likely result in enzymatically activated 6S monomers [46].
Structural studies on complexes between Ca 2+ -S100A4 and NM2A tail peptides revealed a binding interface at the junction of ACD1 and the NHT [106,179,180].The structural information led to the model that S100A4 binds to the NHT to initiate partial unzipping of the coiled-coil which may subsequently destabilize the staggered packing of myosin molecules in the filament and finally result in filament dissociation (Fig. 3) [179,180].The structural basis for this model is based on the observation that the NHT and the C-terminus of the ACD1 wrap around a Ca 2+loaded S100A4, thereby disrupting the ACD and promoting filament disassembly [179].For other NM2A binding partners such as the Arf-GTPase-activating protein ASAP1 and phosphorylation events in the tail are largely paralog-specific.In some but not all cases, phosphorylation has been shown to modulate the delicate equilibrium between the myosin monomer and filament pool in cells [15,50,112,160].For example, tail phosphorylation by PKCξ has been shown to control the assembly state of NM2B and therefore the ability to mechanorespond in cells [15].In vitro, it was shown that CK2 phosphorylation or phosphomimetic mutations at PKC and TRPM7 target sites are insufficient to completely disassemble NM2B tail fragments.Based on this observation, a synergistic effect was proposed in that the accumulation of negative charges through multiple phosphorylation events may weaken the electrostatic interactions between tails in favor of a disassembly pathway for NM2B [161].Interestingly, the effect of phosphorylation on filament stability has been shown to be more pronounced for NM2B than NM2A, leading to the speculation that tail phosphorylation may selectively fine-tune the composition of NM2A/NM2B heterotypic filaments [161].As for studies with NHT deletion mutants, the literature on the biochemistry and consequences of tail phosphorylation often reports conflicting results that are not directly supported by cell biological data.To some extent, this may be attributed to the use of recombinant tail fragments of different lengths that may not represent useful models for full-length myosin, phosphomimetic mutations that often insufficiently mimic the phosphorylated state of the protein, the lack of complex phosphorylation patterns produced by multiple kinases and/ or the absence of regulatory proteins, suggesting that our understanding of the effect of tail phosphorylation is still incomplete [161,[166][167][168].

Interacting partners
Interacting partners can directly and/or indirectly influence myosin activity.They either directly influence the enzyme activity of myosin or interact with the myosin heavy chain.The prime regulator of the enzymatic and functional activity of myosin is filamentous actin, as discussed above.While all actin isoforms stimulate the enzymatic activity of NM2, the extent differs up to ~ 4-fold for NM2A and NM2B [169].Both myosins have increased ATPase activities, coupling efficiencies and in vitro gliding speeds with β-and γ-actin over α-actin [169].NM2C is most potently activated by β-actin [169].Recent cryo-EM structures suggest that the divergent N-termini of actin isoforms adopt distinct conformations that may be sensed by and guide the binding of NM2 paralogs [170].The resulting distinct actomyosin interfaces are likely to contribute to the reported enzymatic and functional differences [170].Posttranslational modifications of the N-termini of actin isoforms such as acetylation and arginylation are predicted to further modulate the 1 3 proposed that NM2s undergo force-dependent conformational changes [196].Negative stain electron microscopy demonstrated that binding of myosin with both motor domains to neighboring sites on an actin filament generates sufficient internal strain to drive load-depending kinetics [189].In addition, structural studies revealed an allosteric communication pathway that connects the active site with the distal end of the motor domain.Mutagenesis experiments suggested that distortion of the converter/lever arm interface under strain may disrupt this pathway and contribute to the reported load-dependent kinetics of NM2s [77].
Together, the mechanokinetic tuning of myosin enzymology and assembly through forces represents an additional layer of NM2 regulation matched to their physiological environment.

Concluding remarks
Recent advances in the field have answered many longstanding questions and revealed an unexpected new complexity of NM2 function and regulation.Remaining and new questions include the existence and cellular roles of the activated 6S monomer, how the tail coiled-coils wind and unwind to assemble or disassemble filaments, the visualization of 10S in cells and probes for the 10S-6S transition, the exact mechanism of NM2 filament formation, and the roles and ultrastructure of NM2 stacks will be addressed with novel technologies in the future to deepen our understanding of the fundamental mechanisms of myosin motor function and to facilitate the development of new research tools and therapeutic strategies for myosin-related diseases.The integration of biochemistry, structural biology, physics, advanced light and electron microscopy will ultimately lead to a more comprehensive and quantitative understanding of NM2 function underlying biological processes and mechanisms in health and disease and provide exciting opportunities for discovery and innovation.

Mechanical forces
Piconewton forces guide and direct the behavior of cells [184].As mechanoenzymes, NM2s not only generate forces by pulling on antiparallel actin filaments but also sense and transmit forces and/or alter the actin cytoskeleton in complex ways.Thereby, NM2s directly and indirectly promote and influence processes including cell mechanics and contractility, mechanosensing, cellular elasticity, cortical tension, and adhesion mechanisms [9,[185][186][187][188].
It has been shown that NM2s are mechanosensitive proteins that sense and respond to chemical and mechanical forces by dynamically changing their enzymatic output in vitro and in cells [59,63,174,[188][189][190][191].This in turn may be sensed by other proteins and lead to coherent cellular responses for example during focal adhesion maturation [186,187].The force-sensitivity of NM2B also contributes to increased tension generation and actin-crosslinking during cytokinesis that resists the expansion of the ring [192].
The altered kinetic pathways that underlie the force-sensitivity of NM2 paralogs are not fully defined yet.In vitro kinetic studies showed that the actin-activated ADP release increases with assisting loads and decreases with resisting loads [189,193].The effect of resisting loads on the ADP release is more pronounced for NM2B (12-fold) compared to NM2A (5-fold).Resisting loads increase the duty ratio and result in long actin attachment lifetimes that may reach into the minute timescale to favor tension maintenance without hydrolyzing ATP [189].Thus, actomyosin interactions can be classified as either catch-or slip-bonds depending upon whether the actin-attachment lifetime increases or decreases with force [97,188].Catch-bond behavior is likely to underlie the force-dependent accumulation of NM2 to stressed parts of the actin cytoskeleton independent of the cellular signaling [15,190,191,194].While it remains controversial whether a mammalian NM2 monomer can move processively, optical trapping studies suggest that the detachment rate of NM2A and NM2B from filamentous actin is reduced under resisting load that slows down the rate of ADP release [66,174].Tropomyosin 4.2-decorated actin filaments have been shown to amplify this effect in vitro with possible implications for the physiological role of this myosin to stabilize specialized cellular actin structures such as stress fibers [174].It is also likely that the force-sensitivity of NM2 paralogs contributes to the 'latch' state in tonic smooth muscle, during which force is maintained for prolonged periods at low rates of ATP consumption [195].
While the precise structural mechanisms for the described force sensitivity have not been fully resolved, it has been

Fig. 2
Fig. 2 Structural features of the motor domain and kinetic cycle of the NM2s a. Key structural features of the myosin motor domain of NM2 paralogs (PDB ID: 5I4E).The myosin motor domain is shown in cartoon representation, the bound nucleotide in spheres.Mg 2+ is shown as green sphere.Light chains are not shown for clarity.b, Key structural features in the nucleotide binding pocket of NM2 paralogs (PDB ID: 5I4E).The myosin motor domain is shown in cartoon rep-

Fig. 3
Fig. 3 Regulation mechanisms of NM2.Select regulation mechanisms of NM2s reviewed in this work.Grey and red font colors indicate regulation mechanisms specific for NM2A and NM2B, respectively.