Gestalt-binding of tropomyosin to actin filaments
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We argue that the overall behavior of tropomyosin on F-actin cannot be easily discerned by examining thin filaments reduced to their smallest interacting units. In isolation, the individual interactions of actin and tropomyosin, by themselves, are too weak to account for the specificity of the system. Instead the association of tropomyosin on actin can only be fully explained after considering the concerted action of the entire acto-tropomyosin system. We propose that the low K a describing tropomyosin:actin interaction, when taken together with the form-fitting complementarity of tropomyosin strands on F-actin and the tendency for tropomyosin to polymerize end-to-end, make possible unique thin filament functions both locally and at higher levels of filament organization.
KeywordsActin Tropomyosin Gestalt Gestalt-binding Gestaltbindung Coiled-coil Troponin Calcium Muscle
Tropomyosin is a two-chained, coiled-coil protein that is found bound to actin filaments in most eukaryotic cells. The tropomyosin coiled-coil itself assumes a helical contour and thus represents a coiled coiled-coil. Tropomyosin molecules link end-to-end to form continuous strands that are wound tightly along the surface of helically disposed actin subunits of thin filaments (for reviews see Perry 2001; Brown and Cohen 2005; Hitchcock-DeGregori 2008; Lehman and Craig 2008). The presence of tropomyosin on actin strengthens thin filaments by increasing their rigidity and reducing their susceptibility to depolymerizing factors. Under the control of troponin and Ca2+ in skeletal and cardiac muscles, and perhaps other factors in most cellular systems including smooth muscles, tropomyosin participates in a molecular switching mechanism to regulate the traffic of myosin motors on actin filaments. Here access of myosin onto actin is gated by tropomyosin, with troponin in the case of striated muscle filaments playing the role of gatekeeper. This is accomplished by azimuthal movement of tropomyosin among different set positions along thin filaments, thereby either exposing or blocking myosin-binding sites on actin (Haselgrove 1972; Huxley 1972; Parry and Squire 1973; Lehman et al. 1994; Vibert et al. 1997; Poole et al. 2006). An intrinsic ability of tropomyosin molecules to undergo such shifts in position on actin at low energy cost is inherent to this steric mechanism (Lehman et al. 2000), and it is troponin that causes tropomyosin to favor one position or another depending on the concentration of Ca2+. This steric mechanism is not just limited to regulating myosin function. Thus, the presence of smooth muscle and non-muscle isoforms of tropomyosin on actin, possibly in concert with caldesmon (Hodgkinson et al. 1997; Hodgkinson 2000; Lehman et al. 2000), no doubt also gate access of a host of cellular actin-binding proteins onto thin filaments (Ishikawa et al. 1989, 1998; Blanchoin et al. 2001; Gunning et al. 2008). However, despite the crucial role played by tropomyosin in actin function, the properties of tropomyosin that contribute to its F-actin binding and lead to its regulatory movements on actin are incompletely understood. In this commentary, we propose a novel mechanism for the tropomyosin–actin association that we call “Gestaltbindung” or “Gestalt-binding” to contrast the interaction with more typically described lock-and-key models involving stereo-specific protein–protein binding. The use of the term is intended to connote several intertwined meanings. Gestalt, a German word for “form”, reflects our argument that the native three-dimensional form taken by tropomyosin is designed to match the actin filament surface, a complementarity which we regard as essential for actin-binding. As in Gestalt-theory [a psychological theory developed by von Ehrenfels (1890) and later by his student Wertheimer (1912)], we also argue that the behavior of the whole system cannot be inferred by examining single “atomistic” units (here single tropomyosin molecules) but only emerges from an understanding of the concerted action of the entire system, viz. the elongated tropomyosin strand as a whole on actin. Finally, we argue that mutations leading to perturbations in tropomyosin shape cause a deficit in “Gestaltbindung”, in which irrelevant conformers, lacking complementarity to the contours of actin, fail to bind to thin filaments, as if the system were divorced from its collective genomic memory.
Tropomyosin is a modular protein with seven pseudo-repeating units designed to bind to and match the polarity of seven adjacent actin monomers along a 385 Å path of the helical strands of actin filaments (Parry 1975; Stewart and McLachlan 1975; McLachlan and Stewart 1976; Phillips et al. 1986; Brown and Cohen 2005). The binding strength of individual tropomyosin molecules to F-actin is very weak [K a ~ 2–5 × 103 M−1, Wegner (1980)]. If each pseudo-repeat module binds actin with roughly equivalent affinity, then the K a of one repeat would be ~3, close to the binding strength of a single salt bridge in proteins, a value so low that thermal energy would readily cause dissociation. The low K a , atypical of actin-binding proteins, indicates that strong stereo-specific interaction is not a significant factor in F-actin–tropomyosin association.
Tropomyosin only binds to actin filaments because of the collective interactions conferred by linking tropomyosin end on end. Estimates for the equilibrium of the tropomyosin end-to-end association are modest [2–4.5 × 102, Wegner (1980)]. However, the overall effect of gluing tropomyosin molecules together over an F-actin substrate significantly raises the effective binding of tropomyosin to thin filaments by many orders of magnitude (in principle to K a 25 for 25 tropomyosin molecules linked in tandem over a 1 μm distance). Thus, it is hardly surprising that altered tropomyosin molecules that are incapable of forming end-to-end links cannot associate appreciably with F-actin (Johnson and Smillie 1977; Heald and Hitchcock-DeGregori 1988; Cho et al. 1990; Monteiro et al. 1994).
The modular design of tropomyosin
In addition to the continuously repeating, seven amino acid long “heptads” that define all α-helical coiled-coils, tropomyosin displays a unique longer-range period that is roughly forty amino acids long (Crick 1953; Stone and Smillie 1978; Parry 1975; Stewart and McLachlan 1975; McLachlan and Stewart 1976; Phillips et al. 1986). The latter accounts for the seven modular domains of tropomyosin, which traverse seven actin-binding partners along thin filaments. Other coiled-coils present in muscle that lack the 7-fold modular periodicity do not bind to actin (e.g. the rod portion of thick filament associated myosin and paramyosin in invertebrates). However, Nature, unlike the Pythagoreans, did not settle on seven-fold motifs as an ideal application of a perfect number. In fact, most somatic cells contain truncated tropomyosin isoforms with four to six ~40 amino acid-long actin-binding modules designed to bind to shorter stretches of thin filaments (Gunning et al. 2005, 2008).
A series of elegant experiments by the Hitchcock-DeGregori and Tobacman groups (Hitchcock-DeGregori and An 1996; Landis et al. 1999; Rosol et al. 2000; Hitchcock-DeGregori et al. 2001, 2002) showed that strict precision in the modular quantization of tropomyosin is essential for actin-binding. Tropomyosin was truncated by deleting one or more internal repeat modules. When the remaining modules were left intact to conform to the actin filament periodicity, these constructs still bound to actin. In contrast, when insertions or deletions were introduced that changed the lengths of one or another of the modules, the actin–tropomyosin alignment was corrupted and actin-binding diminished considerably. Similarly, substitution of random coils in place of coiled-coil modules abolished actin-binding.
Tropomyosin contains strategically placed acidic residues on the surface of each of its repeating modules. These no doubt interact electrostatically with positively charged residues present on the complementary flat face of actin subunits along thin filaments (Lorenz et al. 1995; Brown et al. 2005). Such an interaction is consistent with sensitivity of tropomyosin–actin binding to monovalent ion concentration (Eaton et al. 1975; Hill et al. 1992; Willadsen et al. 1992). Lacking a high-resolution crystal structure of the actin–tropomyosin complex, the positions of interfacial interactions cannot be plotted unambiguously. Nonetheless, in silico modeling provides strong support for the view that complementary surface charges are matched to each other (Lorenz et al. 1995; Brown et al. 2005; Brown and Cohen 2005).
Tropomyosin lies at a high radius on the actin filament
Shape complementarity of tropomyosin and actin filaments
As described, the binding site for tropomyosin on actin is 385 Å long and made of seven low affinity interactions. Surely the only reason that the tropomyosin binds to actin at all is because it assumes the right shape to interact with seven actins all at the same time. This shape can be deduced from high-resolution crystal structures of segments of the molecule that fit very well to contours of tropomyosin in the Lorenz–Holmes atomic model of actin–tropomyosin described above (Brown et al. 2001, 2005; Li et al. 2002, see Fig. 1 B.) These structures also dock extremely well within tropomyosin density envelopes in 3D reconstructions of both Ca2+-treated and Ca2+-free thin filaments (Poole et al. 2006; see Fig. 1 C). No obvious reconfiguration of tropomyosin is needed for the fittings. Thus independently determined tropomyosin structures display a conformation which is directly transposable onto the actin filament, without any apparent need for significant coiled coiled-coil conformational flexibility. Hence, these results indicate that the modular sequence complementary of tropomyosin and F-actin, described above, and the shape complementary, described here, are perfectly correlated. More specifically, these studies not only support the hypothesis that tropomyosin is designed to match the contours of actin but also that it is free to move over a flat actin interface without undergoing an obvious change in configuration (Poole et al. 2006).
The presence of roughly periodic groups of alanine clusters (Conway and Parry 1990) in tropomyosin causes local narrowing and bending of the coiled-coil protein (Brown et al. 2001; Brown and Cohen 2005, also see Nitanai et al. 2007; Minakata et al. 2008). This bending likely is partly responsible for the global coiled coiled-coil shape of tropomyosin, which fits so nicely to the F-actin surface. The B-factor associated with the alanine clusters in crystal structures is low, suggesting that the clusters and their surrounds, while bent, are relatively stable. Formally, alanine clusters can bend a fibrous protein in opposite orientations. In fact, there must be a bias in folding of the tropomyosin-coiled coiled-coil, since crystal structures of tropomyosin fit to right-handed helices that match the right-handed F-actin helix. Thus the whole molecule appears to bend collectively when forming the coiled coiled-coil.
We posit that the inherent helical contour of tropomyosin is an essential feature that facilitates the binding of the elongated protein on actin, weak as this interaction might be. Experimental support for this notion comes from studies showing that replacing core alanine residues, responsible for specific bending, with leucine and valine can reduce the binding of such tropomyosin variants to F-actin (Singh and Hitchcock-DeGregori 2003). This observation suggests that disrupting coiled-coil bending reconfigures the tropomyosin supercoil, which is followed by a concomitant loss of complementarity and hence Gestaltbindung to F-actin. Experimental alteration in tropomyosin pseudo-repeat lengths will also have the same effect. Whether or not such mutations cause changes in flexibility of tropomyosin (Singh and Hitchcock-DeGregori 2003, 2006) may not be as relevant a consideration.
End-to-end polymers of tropomyosin bind tightly to actin filaments
The head-to-tail polymerization of tropomyosin on the surface of actin filaments generates a larger scale level of thin filament organization that is functionally transformative. As mentioned, tropomyosin assembly and binding on actin is only effective once these end-to-end links are formed. In fact, experimental manipulation that interferes with tropomyosin strand formation (e.g. expressing unacetylated tropomyosin constructs or removing tropomyosin ends) fixes the system at the lower level of organization and prevents effective actin-binding (Johnson and Smillie 1977; Heald and Hitchcock-DeGregori 1988; Cho et al. 1990; Monteiro et al. 1994). There appear to be multiple mechanisms for ensuring that distinctive ends of different tropomyosin isoforms adhere to each other and several structural models have been offered for the process (McLachlan and Stewart 1976; Greenfield et al. 2006; Murakami et al. 2008). Understanding the specificity of the tropomyosin–tropomyosin connections is important. However, of possible greater importance is recognition that only minimum energy cost may be needed to bias tropomyosin into polymeric strands and thus allow the protein to work as part of an unbroken cooperative system, where Aristotle’s dictum, “The whole is more than the sum of its parts” applies. The Gestalt of the thin filament system as a whole can only then structure how the parts behave.
Clear and convincing evidence indicates that, in the complete absence of any accompanying actin-binding proteins, muscle and non-muscle isoforms of tropomyosin bind to actin with great precision and regularity (Lorenz et al. 1995; Lehman et al. 2000; Skoumpla et al. 2007; Maytum et al. 2008). Binding of the two proteins to each other is an innate property that is intrinsic to the design of tropomyosin and actin filaments. However, given the diversity of tropomyosin isoforms, particularly those in non-muscle cells (Gunning et al. 2005, 2008), it is not surprising that different tropomyosins show differences in their affinity for actin (Pittenger et al. 1995). This potentially could result from subtle changes in surface charge, in overall coiled coiled-coil shape and flexibility, or in the end-to-end molecular bonding of tropomyosin. It is also possible that extrinsic factors such as ancillary actin-binding proteins may modulate the conformational landscape of the actin filament to influence Gestalt-binding (cf. Hill et al. 1992). In addition, actin or tropomyosin binding proteins such as troponin-T and caldesmon may tether tropomyosin to actin, thus stabilizing assembled thin filaments (Hill et al. 1992; Pittenger et al. 1995).
Proposed scheme for tropomyosin binding to actin filaments
We thank Ms. Karen Moore (Moore Design) for artwork in Fig. 2. We also thank the restaurant staff at Schloss Schwetzingen for allowing the authors to first discuss Gestaltbindung a bit past closing hours. This research was supported by grants from the National Institutes of Health to W.L. (HL36153, HL86655).
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