Abstract
To investigate the molecular interactions of sodium dodecyl sulfate (SDS) with human ubiquitin and its unfolding mechanisms, a comparative study was conducted on the interactions of the protein in the presence and absence of SDS at different temperatures using six independent 500 ns atomistic molecular dynamics (MD) simulations. Moreover, the effects of partial atomic charges on SDS aggregation and micellar structures were investigated at high SDS concentrations. The results demonstrated that human ubiquitin retains its native-like structure in the presence of SDS and pure water at 300 K, while the conformation adopts an unfolded state at a high temperature. In addition, it was found that both SDS self-assembly and the conformation of the resulting protein may have a significant effect of reducing the partial atomic charges. The simulations at 370 K provided evidence that the SDS molecules disrupted the first hydration shell and expanded the hydrophobic core of ubiquitin, resulting in complete protein unfolding. According to these results, SDS and temperature are both required to induce a completely unfolded state under ambient conditions. We believe that these findings could be useful in protein folding/unfolding studies and structural biology.
Similar content being viewed by others
Introduction
Surfactants or surface active agents are used in a broad range of applications in pharmaceutical industries and biological studies, including solubilizing membrane proteins, and in crystallography studies1,2,3. They are extensively used in biochemistry and biotechnology (e.g., in sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and in probing the protein’s folding/unfolding mechanisms)4,5,6,7,8,9,10,11. Anionic surfactants are the most commonly used surfactant. Two examples of their applications are denaturing globular proteins and modifying the activities of enzymes. The surfactant-protein interactions depend on the intrinsic properties of both the surfactant and the protein, especially the alkyl chain length and the hydrophilic head group charge of the surfactant4,8. SDS is a well-known ionic detergent, consisting of a hydrophobic 12-carbon chain and a polar sulfate head group whose chemical properties and applications are more extensively investigated than the other surfactants12. SDS strongly binds to the positively charged and the hydrophobic residues of proteins through its sulfate groups and alkyl chains, respectively13. Accordingly, it is a valuable detergent in the field of structural biology and protein folding/unfolding studies. For example, it can induce the formation of α-helices in a protein structure7,14,15. SDS induces cooperative unfolding in proteins such as bovine serum albumin (BSA), hen egg white lysozyme, α-lactalbumin, and β-lactoglobulin structures at high concentrations16,17,18,19,20,21. Although SDS can denature proteins, the addition of nonionic surfactants, including octaethylene glycolmonododecyl ether (C12E8) and n-dodecyl-β-D-maltopyranoside (DDM) in the SDS-protein solution, induces refolding of proteins11. The nonionic surfactants tend to interact with each other rather than with proteins, and they weakly react with proteins5. Additionally, they can protect the conformations of proteins from unfolding induced by the anionic surfactants5,22.
The structure of the SDS micelles, which is dependent on the detergent concentrations, can affect the unfolding rate of proteins. By increasing the SDS concentrations, the micellar structure shifts from spherical to cylindrical. Hence, the unfolding rate of mixed α/β proteins in the presence of cylindrical micelles directly depends on the micellar concentration4. The structure of the SDS surfactant is similar to the phospholipid molecules of the membrane (i.e., it has a hydrophilic head group and a hydrophobic tail). Therefore, the molecule can mimic a biological membrane environment23,24,25,26,27,28. Moreover, the interactions between proteins and phospholipids are associated with different protein aggregation diseases through promoting or avoiding the aggregations29,30,31,32.
Ubiquitin is a small and a heat stable protein with 76 amino acid residues, and it contains 11 acidic and 11 basic amino acids along with a mixed α/β secondary structure29,33. The protein has been called ubiquitin because it is ubiquitous and can be present on the surface of membranes, in the cytoplasm, and in the nucleus of different eukaryotic cells33. Ubiquitin is classified under a family of protein modifiers, which have the same structure but different amino acid sequences34,35,36. In different organisms, the amino acid sequence of ubiquitin varies by only a few residues; therefore, it is considered as one of the highly conserved proteins in eukaryotic organisms33,37. In eukaryotic cells, ubiquitin is involved in proteolytic and non-proteolytic pathways. In the proteolytic pathway, the protein gets covalently attached to a target protein which leads to the transportation of the protein to the proteasome system34,37. In the non-proteolytic pathway, however, ubiquitin is engaged in activities such as membrane protein transport38, DNA repair39, removable of abnormal proteins by chaperones40, and protein folding41, among many other crucial activities37,42,43.
The aim of the present study was to investigate the responses, the conformational changes, and the unfolding mechanisms of human ubiquitin in the presence of SDS surfactant at the atomic level of detail. To better understand the effects of SDS on ubiquitin structure, we additionally conducted two independent all-atom molecular dynamics (MD) simulations of ubiquitin in pure water at two ambient temperatures. The results indicated that in the presence of high SDS concentrations and high temperature, human ubiquitin completely lost its secondary structures and adopted a random coil structure, while the SDS molecules stabilized the protein’s native structure at low temperature. The results also revealed that at high temperatures the SDS surfactants adopt a membrane-like structure and the hydrophobic core of the protein is destroyed by SDS molecules.
Computational Methods
Molecular dynamics simulation
All MD simulations were conducted using the GROMACS 4.5.6 simulation package44,45,46. The initial coordinates of the human ubiquitin were taken from the Protein Data Bank (PDB ID: 1UBQ) (Fig. 1)33. The primary structure of the SDS molecule was obtained from the previous study47, and its partial atomic charges and parameters were obtained from the automated force field topology builder database (ATB)48, which is based on the GROMOS96 53A6 force field. For S5 and S6 simulations, we first generated the itp file of SDS by the ATB server then reduced the partial atomic charges of each SDS atom based on the partial atomic charges created by the PRODRG server49.
The GROMOS96 53A6 force field was applied to all simulations and the simple point charge (SPC) water model was used to provide the solvation conditions for ubiquitin50. All systems were electrostatically neutralized using the counter-ions Cl- and Na+. The periodic boundary conditions were considered to avoid possible boundary effect problems. The Particle Mesh Ewald (PME) algorithm and a 1.2 nm distance cutoff were applied for the long-range and the short-range electrostatic interactions51, respectively. The temperature and pressure were retained using a Nose–Hoover algorithm (at 300 K and 370 K) and a semi-isotropic Parrinello–Rahman algorithm (at 1 atm)52,53,54, respectively. In all MD simulation systems, the steepest descent method was considered for energy minimization and each system was equilibrated under NVT-ensemble and NPT-ensemble states. Further information for all MD simulations is listed in Table 1.
Calculation of free energy
The g_mmpbsa tools were used to calculate the binding free energy, which calculates the free energy using the Molecular Mechanics-Poisson Boltzmann Surface Area (MM-PBSA) method55,56. In principle, the binding free energy of each system can be calculated using the following equation (Eq. 1)
where ΔG binding is the total free energy of the complex, minus the total free energy of each complex component in its free state. This value is equal to the total polar binding free energy plus the total non-polar binding free energy of the complex. Therefore, the following equation was used to calculate the average binding free energy (Eq. 2)
where ΔGpb and ΔGnpb are the polar binding free energy and the non-polar binding free energy, respectively, and can be obtained as (Eqs 3, 4)
where ΔGpols and ΔGnpols are polar and non-polar energies of solvation, respectively. ΔGelec is the electrostatic energy and ΔGvdw is the van der Waals energy. In the MM-PBSA method, a specified number of snapshots of trajectory, based on the number of steps in the trajectory, is used to calculate the average binding energy of the molecular dynamics system57. In each system, 313 snapshots during the simulation time were extracted for the calculation of the average binding energy because the number of steps in the molecular dynamics trajectory was 313 steps.
Results and Discussion
Effects of SDS molecules on the secondary structures, compactness, and tertiary structure of ubiquitin
Ubiquitin is a heat-stable protein, and its thermal stability depends on ambient pH. However, at neutral pH (our simulation conditions) its melting temperature is ≥100 °C58. We first performed the Dictionary Secondary Structure of Proteins (DSSP) analysis to identify the secondary structures of each ubiquitin residue in all MD simulations (Fig. 2). As observed, the ubiquitin secondary structures began to unfold at 370 K and lost its helical contents in pure water, which is in agreement with the aforementioned experimental study58. Probably, the fully unfolded state can be observed with an increased simulation time scale, as in one of the replications, it was observed after approximately 300 ns of MD simulation (Supplementary Figure S1). The DSSP analyses also revealed that the secondary structure elements are intact in the pure water at 300 K (Fig. 2(a)).
Above the critical micelle concentration (CMC), SDS can induce or maintain the helical structures of proteins23,59. Gregory et al. used capillary electrophoresis (CE) and a circular dichroism (CD) spectrophotometer to understand the SDS-ubiquitin interactions. They have also indicated that the increased SDS molecule counts in the ubiquitin-SDSn complex (e.g., ubiquitin-SDS11, ubiquitin-SDS25, and ubiquitin-SDS33) increases the alpha-helical contents of ubiquitin with respect to the native structure60. Moreover, in the SDS concentrations below 2 mM, in which ubiquitin bonds to approximately 11 SDS molecules, the protein maintains its native-like secondary structures. As shown in Fig. 2(c), the helical structure of ubiquitin in the presence of SDS was maintained at 300 K, and the protein retained its native-like structure in the presence of 111 SDS molecules ([SDS] ≈ 1.3 M, the CMC value for SDS in pure water is 7–8 mM) during the 500 ns MD simulation. To confirm this result, we extended one of the simulation replications to 1000 ns so that the native structure of the protein was still maintained (Supplementary Figure S2). Previous studies have revealed that the β-sheet strands of proteins are stable against SDS surfactants5,61. In good agreement with these results, Fig. 2(c) shows that in the presence of SDS the β-sheet strands of ubiquitin were maintained during the MD simulations at 300 K. An experimental study on human serum albumin (HSA) has also indicated that beyond 90 °C (~360 K) the helical structures of the protein were disrupted in the presence of SDS9. However, at temperatures below 80 °C (~353 K), the helical structure of the protein could be more effectively protected at a low concentration of SDS (1:20 molar ratio of SDS to HSA) than in the absence of SDS. As shown in Fig. 2, ubiquitin began to unfold gradually in the SDS micelles at 370 K. Hence, with increasing the simulation time, the protein completely lost its α-helix and most of its β-sheet contents and adopted a random coil structure (Fig. 2 and Supplementary Figure S1).
The radius of gyration (Rg) analysis can provide information about the structural compactness of proteins. Therefore, to identify the compactness changes of ubiquitin, we conducted the Rg analysis for all simulations. As observed in Fig. 3(a), in S2 and at most points over the simulation, the Rg values of ubiquitin were larger than those of the S1 and S3 simulations. The Rg values of the protein in the S1 and S3 simulations were nearly constant, while these values in the S4 simulation were remarkably larger than the others and steadily increased during the MD simulations. These larger values in the S4 simulation were expected because the protein adopted a random coil structure, considering the results of the DSSP analysis (Fig. 2(d) and Supplementary Figure S1). Moreover, the average of Rg and solvent accessible surface areas (SASA) were calculated for all simulation replications (Table 2). As shown in Table 2, the ubiquitin conformation in the presence and absence of the SDS molecules at 300 K has the lowest SASA and Rg values, and this suggests a high compactness in the protein structure when compared to 370 K. As mentioned previously, at high temperatures and SDS concentrations, the responses of the protein to the surfactant completely changed and it lost the α-helix and β-sheet structures under ambient conditions. Consequently, during the 500 ns simulation time, the high temperature cannot be the only factor for denaturing the protein structure because it has the β-sheet strands in pure water at 370 K (Fig. 2(b)). In addition, both SDS and high temperature caused global unfolding and the protein could not be stable under these environmental conditions, even for the β-sheet secondary structures that are usually SDS resistant. It seems SDS acts as a cooperative factor for the thermal denaturation of the protein. This is in agreement with the experimental studies9.
The helical structures are retained by the intramolecular hydrogen bonding network that is independent of the tertiary structure of proteins. Therefore, they can be effectively disrupted by the SDS surfactants. The rate of denaturation of the β-sheet strands depends on the total unfolding of the proteins because they can make global contacts in the protein structure5. To determine the stability of the helical structures in the simulations, we calculated the number of internal hydrogen bonds in the ubiquitin helices and as the average of helical angle per residue. As demonstrated in Fig. 3(b,c), the number of hydrogen bonds in both S2 and S4 simulations was extensively reduced, implying the decrease in the α-helical content under these conditions. However, the value in the S1 simulation was nearly the same as the S3 simulation and the median number of hydrogen bonds for the helical segment was eight. For an α-helix structure, the value of the helical angle is 100°. It is clear that at 300 K the helical angle values were nearly constant and had an average of approximately 101° in all replications (Fig. 3(c)). In the S2 and S4 simulations, a wider distribution of helical angles can be observed, suggesting that there are unstable helical structures.
To identify the tertiary structure changes in all simulations, we computed the average smallest distances between the residue pairs of ubiquitin in the first and last snapshots of all simulations (Figs 4 and 5). As shown in Fig. 4(a,b), the minimum distance matrix of the first snapshot was the same as the last step in the S1 simulation, which suggests that the protein maintained its native conformation under this condition. In the S2 simulation, the blue regions in the distance matrix of the last snapshot were more than that of the first snapshot, which indicates an increase in the smallest distance between the pair of residues (Fig. 4(c,d). The total pattern of the matrix was not changed remarkably, which confirms a partial maintenance of the globular structure and the local unfolding in the protein conformation. We also observed the same behavior as in the S1 simulation for the protein in the S3 simulation (Fig. 5(a,b)). The wider blue area in Fig. 5(b) indicates that there are more distances between residues than the first step and confirms the occurrence of global unfolding in the S4 simulation (Fig. 5(c,d)).
Free Energy Landscape
To further investigate of the stability and compactness of the ubiquitin structure, we calculated the free energy landscape (FEL), which can be obtained by the following equation (Eq. 5):
where A is the order parameter, which in the present study is Rg and the Cα root mean square deviation (RMSD). PA and PB are the probabilities of finding the system in the A and B states, respectively. PB is the maximal probability. ΔG A is the corresponding free energy at the A state and KB and T represent the Boltzmann constant and temperature, respectively.
SDS has been reported as a stabilizer of the protein structure for STY3178, a mixed α/β protein10. The contour plots of FEL in Fig. 6(a,b) shows that the protein was stable at 300 K and the range of green basins was smaller in the presence of SDS compared to its absence. This indicates that in the S3 simulation, the protein structure is slightly more stable, and it has the smallest values for Rg and RMSD compared to those in the simulations. Furthermore, in the S1 and S3 simulations, a deeper valley (ΔG = 0), centered around 1.2 nm and 0.22 nm, was observed. The results suggested that the most stable conformation of human ubiquitin could be obtained when the Rg and RMSD values are approximately 1.2 nm and 0.22 nm, respectively. In the S2 and S4 simulations (Fig. 6(c,d)), the deeper valley did not assign to a single point, which demonstrates the minimum free energy (ΔG = 0) becomes unstable at 370 K.
A wider distribution along the RMSD axis can be observed in the S2 simulation compared to the S1 and S3 simulations. It confirmed the local unfolding of the protein because the compactness of the protein (Rg) did not significantly change when compared with the S1 and S3 simulations. Moreover, there were the higher fluctuations in the protein structure. Finally, in the case of the S4 simulation, the green, yellow, and red basins of the FEL plot extend along the RMSD and Rg axes, which show the highest fluctuations of ubiquitin at high SDS concentrations and high temperatures. Moreover, it confirmed that the protein completely lost its native compactness and, therefore, global unfolding occurred under this condition.
The effects of micelle structures on the ubiquitin conformation
One of the important issues that affect the unfolding mechanism of proteins by SDS surfactants is the micellar structures. Changes in the structure of micelle can affect the denaturing power of the SDS molecules so that the lower power has been dedicated to simple micelle structures4. The binding of a detergent to the protein in the monomeric form may induce some local changes. However, the global unfolding of the protein occurs only in higher detergent concentrations21.
In the present study, the SDS surfactants were used at concentrations above the CMC (111 SDS molecules, [SDS] ≈ 1.3 M). In this condition, SDS molecules are expected to induce denatured states in the protein structure by global contacts. Under these conditions, in the SDS micelles, some independent simple micelle structures have been formed so that all of them could not continuously interact with the protein (Fig. 7(a)). These micellar structures can induce local changes, but they are unable to induce global protein unfolding. In the S5 simulation, the SDS molecules are uniformly distributed around the protein conformation and may induce protective effects on the tertiary structure of the protein (Fig. 7(c)). In this simulation, the hydrophobic tails of SDS molecules saturated the surface of ubiquitin more than in the S3 simulation, which agrees with the results of the non-polar binding energies (Table 3).
The structure of micelles in the S6 simulation was different from that in the S4 simulation and could not induce significant changes in the protein conformation (Fig. 7(d)). The SDS surfactants adopted a membrane-like structure at high concentrations and high temperature (S4) and they gradually repelled ubiquitin out of the hydrophobic core. Therefore, the protein was completely unfolded on the hydrophilic surface of the SDS mimic-membrane (Fig. 8(a–f)). The low tendency to keep ubiquitin in the hydrophobic core is reasonable because ubiquitin is a very soluble protein and it needs hydrophilic surfaces to bind. Therefore, it moved to the hydrophilic interface which is composed of the SDS headgroups and water molecules. Previous studies have indicated that the local unfolding of proteins occurs with the monomeric forms of detergent, whereas surfactants lead to global unfolding at concentrations above the CMC4 or in the formed micelles5. The global unfolding of ubiquitin in the presence of SDS molecules at high temperatures could be because of the global binding of the SDS micelles to the protein, as observed in Fig. 7(b).
The protein denaturing potency of negatively charged surfactants depends on their total negative charges in the micellar form5. Therefore, it could be that in the S4 simulation, the global electrostatic interactions with ubiquitin play important roles in the protein unfolding (see Table 3).
The step by step unfolding of ubiquitin
Previous studies have indicated that the hydrophobic core of ubiquitin is composed of the Ile3, Val5, Ile13, Leu15, Val17, Ile23, Val26, Ile30, Leu43, Leu50, Leu56, and Leu67 residues62. They have also found that the ubiquitin core, specifically Val26, is critical for the conformational stability of the protein. It has been shown that binding of the SDS micelles to mixed α/β proteins initially extends the protein structure, leading to the denaturation of protein slightly before the global unfolding4. To find the main factor in the ubiquitin unfolding with the SDS micelles at 370 K, we first investigated the roles of electrostatic attractions and then explored the effects of the SDS molecules on the hydrophobic core of the protein. A previous experimental study indicated that the acetylation of lysine residues inhibits the binding of SDS to human ubiquitin. Additionally, it has been shown that the electrostatic attractions are crucial for the binding of SDS molecules to the protein29. Anand et al. have established that initial electrostatic interactions between the SDS sulfate head groups and the oppositely charged residues of HSA induce partial denaturation in the protein structure6. To obtain more insight into the roles of the electrostatic interactions in the unfolding mechanism of ubiquitin, we reduced the partial atomic charges of the SDS molecule and repeated the MD simulations at 300 K and 370 K. Interestingly, our results indicated that the human ubiquitin maintained its native conformation in both simulations. Based on the DSSP analyses (Fig. 2(e,f)), it seems that reducing the partial atomic charges causes SDS to act as a stabilizer for the protein structure at either 300 K or 370 K. These results imply the relevance of the electrostatic interactions in the unfolding mechanism of the protein.
As seen in Fig. 9(a), the basic residues of ubiquitin are distributed throughout the tertiary structure of the protein and are surrounded by the hydrophobic core. In the S4 simulation, the affinity of basic residues to make strong electrostatic interactions with SDS molecules was greater than in the S6 simulation because the SDS molecules had higher partial atomic charges (Table 3). The repulsions between the anionic side chains and the SDS sulfate groups can rule out the unfolding rate and stability of mixed α/β proteins4. Therefore, increasing the partial atomic charges in the S4 simulation would also increase the electrostatic repulsions between the acidic residues and the head groups of the SDS molecules. However, increased temperature and hydrophobic interactions may also be involved.
Previous studies have shown that SDS binds to the protein structure in the positively charged surface areas and then alters the binding to the neighboring hydrophobic residues8,29. Therefore, the stronger electrostatic interactions in the S4 simulation, as well as a high temperature, could induce the structural stress and may lead to Leu43, which is next to Arg42, leaving the hydrophobic core as the starting point of the unfolding process (Fig. 9(c)). As mentioned, the hydrophobic core of ubiquitin contributes to the protein’s stability. Therefore, it is likely that the ubiquitin hydrophobic core is a good attack point for the SDS molecules at 370 K.
After Leu43, the hydrophobic interactions of the SDS tails affect the internal interactions of Leu67 with the hydrophobic core and result in the removable of the residue from the hydrophobic core (Fig. 9(d)). Leu43 and Leu67 leaving the hydrophobic core provides an opportunity for the SDS molecules to insert into the hydrophobic core of the protein (zoom out in Fig. 9(d)). These molecules affect the internal hydrophobic interactions and lead to Ile23, Leu50, and Leu56 leaving the hydrophobic core (Fig. 9(e)). In addition, the rest of the hydrophobic core residues are still stable until Val26 and Ile30 leave the hydrophobic core (Fig. 9(f)) and global unfolding takes place (Fig. 9(g)). As mentioned, Val26 is crucial for the protein stabilization, and the residue has remained more stable and left the hydrophobic core later than the other residues.
To corroborate the insertion of SDS molecules into the hydrophobic core of ubiquitin, we calculated the minimum distance between the SDS tails and the residues of the hydrophobic core (Fig. 10). The results indicated that in the S3, S5, and S6 simulations, at some points during the simulations, the SDS molecules approached the hydrophobic core but they remained at a nearly constant distance away from the hydrophobic core. However, in the S4 simulation, the minimum distance plot reached a plateau below the minimum distance plot of the others. The average minimum distances of SDS molecules were 0.46 ± 0.05 nm, 0.44 ± 0.07 nm, and 0.51 ± 0.08 nm in the S3, S5, and S6 simulations, respectively. This value for the S4 simulation was 0.33 ± 0.27 nm, which indicated that the SDS molecules inserted into the hydrophobic core more favorably than others. Indeed, because of the high temperature at 370 K, the protein begins to partially unfold, and this makes an opportunity for SDS molecules to attack the hydrophobic core and disrupt the internal hydrophobic interactions.
Binding free energies
To identify which type of the interactions plays the main role in the protein unfolding, we additionally calculated the van der Waals, electrostatic, and nonpolar interactions between the SDS molecules and ubiquitin in the S3, S4, S5, and S6 simulations (Table 3). As demonstrated, both nonpolar and van der Waals interactions were favorable in all simulations, which can be related to the high SDS concentrations (above the CMC). The nonpolar binding free energies (ΔG npb ) for the S3, S4, S5, and S6 simulations were −419.2 Kj/mol, −771.2 Kj/mol, −670.7 Kj/mol, and −302.4 Kj/mol, respectively. In all simulations, the hydrophobic interactions predominated because of the high SDS concentrations and saturation of the protein surface by the SDS hydrophobic tails, which is in agreement with previous studies23,26,63. These findings suggest that the nonpolar interactions, especially the van der Walls forces, are involved in the interactions of surfactants with ubiquitin at high SDS concentrations. In the S4 simulation, not only were the nonpolar binding energies higher than those of the others, but the electrostatic interactions were also favorable (−10.5 Kj/mol). Furthermore, the total binding energies were higher than the others, indicating that the SDS molecules bind to the protein tightly and lead to global unfolding.
To investigate the binding of SDS molecules to the protein, the total number of contacts between ubiquitin, SDS and water molecules was computed (Table 4). In the S4 simulation, the number of contacts between the protein and water molecules was decreased while it was increased for the protein-SDS complex. These results, as well as the calculated free energies in Table 3, are in good agreement with a previous experimental study on the HSA protein9. They have indicated that with increasing the SDS concentrations at temperatures above 80 °C, the strength of contacts between SDS and the protein gradually increased.
Effects of SDS on the hydration shell of ubiquitin
The median number of water and SDS molecules in the first hydration shell of the protein was calculated for all simulation systems within R = 0.5 nm64 (Table 5). As indicated, the number of water molecules around ubiquitin in the S3 and S4 simulations was remarkably reduced compared to the S1 and S2 simulations because SDS molecules exist in the first hydration shell. The total number of water molecules in the hydration shell (WN) of the protein is not constant and this value changes when protein reactions occur65. As shown in Table 5, the WN in S3 simulation was more than that of the S4 simulation, suggesting that at a high temperature the water molecules were repelled by SDS. It was confirmed by calculating the number of SDS molecules in the first hydration shell, which in the S4 simulation was significantly more than in the S3 simulation. The total number of hydrogen bonds (HN) in the S2 simulation was less than those in the S1 simulation, and this is maybe one of the reasons for the local unfolding in the ubiquitin conformation. The HN value in the S1 simulation was 172, indicating the number of hydrogen bonds which are required for retaining the native conformation of the protein. Our results indicated that the total number of hydrogen bonds made by SDS and water molecules was 170 (146 + 24), providing the HN value which is required in the first hydration shell. Therefore, ubiquitin maintained its native structure in the presence of SDS micelles at 300 K, which was the same as seen in the S1 simulation. In the S4 simulation, the total number of hydrogen bonds made by the SDS and water molecules (129 + 21) was less than that made by only the water molecules in the S2 simulation (166). Possibly, at a high temperature, the SDS and water molecules could not provide the required hydrogen bonds and the first hydration shell around the protein was disrupted and then global unfolding occurred. The hydration shell is determined by the stabilized conformation of proteins, besides the hydrogen bonds, hydrophobic interactions, and van der Waals interactions.
Summary
The current study provides information that the surfactant stabilizes the ubiquitin conformation at low temperatures and high SDS concentrations. The Rg and DSSP analyses revealed that ubiquitin loses its native conformation and adopts a random coil structure over the entire simulation time. The results also suggested that the partial atomic charges not only can affect the type and level of interactions in the protein-SDS complex but also can change the orientation, distribution, and assembly of SDS molecules. Moreover, we demonstrated that the SDS surfactant aggregates to form a membrane-like structure and induces global unfolding in the protein conformation at high temperatures. This study demonstrates that maintaining the hydration shell plays an important role in the unfolding mechanism of ubiquitin. The MD simulations also indicated that neither SDS molecules nor temperature can be used alone for inducing the fully unfolded state in the protein structure and both are required. We believe that these findings could be useful in protein biochemistry, protein folding/unfolding and structural biology. Additionally, the SDS surfactant can mimic the biological membrane environment, and investigating its interactions with proteins are of interest in the field of membrane biology. Therefore, our findings can be productive and helpful for any direct examinations of ubiquitin-membrane interactions.
References
Tejaswi Naidu, K. & Prakash Prabhu, N. Protein - Surfactant Interaction: SDS Induced Unfolding of Ribonuclease A. J. Phys. Chem. B 14760–14767; https://doi.org/10.1021/jp2062496 (2011).
Duquesne, K. & Sturgis, J. N. Membrane protein solubilization. Methods Mol. Biol. 601, 205–217 (2010).
Prive, G. G. Detergents for the stabilization and crystallization of membrane proteins. Methods 41, 388–397 (2007).
Otzen, D. E. Protein Unfolding in Detergents: Effect of Micelle Structure, Ionic Strength, pH, and Temperature. Biophys. J. 83, 2219–2230 (2002).
Nielsen, M. M., Andersen, K. K., Westh, P. & Otzen, D. E. Unfolding of β-Sheet Proteins in SDS. Biophys. J. 92, 3674–3685 (2007).
Anand, U., Jash, C. & Mukherjee, S. Spectroscopic probing of the microenvironment in a protein-surfactant assembly. J. Phys. Chem. B 114, 15839–15845 (2010).
Otzen, D. E. & Oliveberg, M. Burst-phase expansion of native protein prior to global unfolding in SDS. J. Mol. Biol. 315, 1231–1240 (2002).
Otzen, D. E. Proteins in a brave new surfactant world. Curr. Opin. Colloid Interface Sci. 20, 161–169 (2015).
Moriyama, Y. & Takeda, K. Secondary Structural Changes of Intact and Disulfide Bridges-Cleaved Human Serum Albumins in Thermal Denaturation up to 130 °C – Additive Effects of Sodium Dodecyl Sulfate on theChanges. J. Oleo Sci. 529, 521–529 (2017).
Saha, P., Sikdar, S., Manna, C., Chakrabarti, J. & Ghosh, M. SDS induced dissociation of STY3178 oligomer: experimental and molecular dynamics studies. RSC Adv. 7, 6209–6214 (2017).
Kaspersen, J. D., Søndergaard, A., Madsen, D. J., Otzen, D. E. & Pedersen, J. S. Refolding of SDS-Unfolded Proteins by Nonionic Surfactants. Biophys. J. 112, 1609–1620 (2017).
Li, J., Fan, T., Xu, Y. & Wu, X. Ionic liquids as modulators of physicochemical properties and nanostructures of sodium dodecyl sulfate in aqueous solutions and potential application in pesticide microemulsions. Phys. Chem. Chem. Phys. 0, 1–3 (2016).
Hansen, J. H. et al. Stable intermediates determine proteins’ primary unfolding sites in the presence of surfactants. Biopolymers 91, 221–231 (2009).
Jirgensons, B. Effects of n-propyl alcohol and detergents on the optical rotatory dispersion of alpha-chymotrypsinogen, beta-casein, histone fraction F1, and soybean trypsin inhibitor. J. Biol. Chem. 242, 912–918 (1967).
Mattice, W. L., Riser, J. M. & Clark, D. S. Conformational properties of the complexes formed by proteins and sodium dodecyl sulfate. Biochemistry 15, 4264–4272 (1976).
Anand, U., Ray, S., Ghosh, S., Banerjee, R. & Mukherjee, S. Structural Aspects of a Protein–Surfactant Assembly: Native and Reduced States of Human Serum Albumin. Protein J. 34, 147–157 (2015).
Hansted, J. G., Wejse, P. L., Bertelsen, H. & Otzen, D. E. Effect of protein–surfactant interactions on aggregation of β-lactoglobulin. Biochim. Biophys. Acta - Proteins Proteomics 1814, 713–723 (2011).
Otzen, D. E., Sehgal, P. & Westh, P. α-Lactalbumin is unfolded by all classes of surfactants but by different mechanisms. J. Colloid Interface Sci. 329, 273–283 (2009).
Lad, M. D., Ledger, V. M., Briggs, B., Green, R. J. & Frazier, R. A. Analysis of the SDS−Lysozyme Binding Isotherm. Langmuir 19, 5098–5103 (2003).
Waninge, R., Paulsson, M., Nylander, T., Ninham, B. & Sellers, P. Binding of Sodium Dodecyl Sulphate and Dodecyl Trimethyl Ammonium Chloride to β-Lactoglobulin: A Calorimetric Study. Int. Dairy J. 8, 141–148 (1998).
Clarke, S. The hydrophobic effect: Formation of micelles and biological membranes, 2nd edition (Tanford, Charles). J. Chem. Educ. 58, A246 (1981).
Otzen, D. Protein-surfactant interactions: A tale of many states. Biochim. Biophys. Acta - Proteins Proteomics 1814, 562–591 (2011).
Jafari, M. & Mehrnejad, F. Molecular Insight into Human Lysozyme and Its Ability to Form Amyloid Fibrils in High Concentrations of Sodium Dodecyl Sulfate: A View from Molecular Dynamics Simulations. PLoS One 11, e0165213 (2016).
Kumar, E. K., Qumar, S. & Prabhu, N. P. Sodium dodecyl sulphate (SDS) induced changes in propensity and kinetics of alpha-lactalbumin fibrillation. Int. J. Biol. Macromol. 81, 754–758 (2015).
Khan, J. M. et al. SDS can be utilized as an amyloid inducer: A case study on diverse proteins. PLoS One 7 (2012).
Hung, Y.-T., Lin, M.-S., Chen, W.-Y. & Wang, S. S.-S. Investigating the effects of sodium dodecyl sulfate on the aggregative behavior of hen egg-white lysozyme at acidic pH. Colloids Surf. B. Biointerfaces 81, 141–51 (2010).
Sureshbabu, N., Kirubagaran, R. & Jayakumar, R. Surfactant-induced conformational transition of amyloid beta-peptide. Eur. Biophys. J. 38, 355–367 (2009).
Yagi, H., Ban, T., Morigaki, K., Naiki, H. & Goto, Y. Visualization and classification of amyloid beta supramolecular assemblies. Biochemistry 46, 15009–15017 (2007).
Shaw, B. F. et al. Complexes of native ubiquitin and dodecyl sulfate illustrate the nature of hydrophobic and electrostatic interactions in the binding of proteins and surfactants. J. Am. Chem. Soc. 133, 17681–17695 (2011).
Bodner, C. R., Maltsev, A. S., Dobson, C. M. & Bax, A. Differential phospholipid binding of alpha-synuclein variants implicated in Parkinson’s disease revealed by solution NMR spectroscopy. Biochemistry 49, 862–871 (2010).
Bodner, C. R., Dobson, C. M. & Bax, A. Multiple tight phospholipid-binding modes of alpha-synuclein revealed by solution NMR spectroscopy. J. Mol. Biol. 390, 775–790 (2009).
Vamvaca, K., Volles, M. J. & Lansbury, P. T. J. The first N-terminal amino acids of alpha-synuclein are essential for alpha-helical structure formation in vitro and membrane binding in yeast. J. Mol. Biol. 389, 413–424 (2009).
Vijay-Kumar, S., Bugg, C. E. & Cook, W. J. Structure of ubiquitin refined at 1.8 A resolution. J. Mol. Biol. 194, 531–544 (1987).
Pickart, C. M. & Eddins, M. J. Ubiquitin: Structures, functions, mechanisms. Biochim. Biophys. Acta - Mol. Cell Res. 1695, 55–72 (2004).
Hochstrasser, M. Evolution and function of ubiquitin-like protein-conjugation systems. Nat. Cell Biol. 2, E153–7 (2000).
Jentsch, S. & Pyrowolakis, G. Ubiquitin and its kin: how close are the family ties? Trends Cell Biol. 10, 335–342 (2000).
Pickart, C. M. Back to the Future with Ubiquitin. Cell 116, 181–190 (2004).
Hicke, L. & Dunn, R. Regulation of membrane protein transport by ubiquitin and ubiquitin-binding proteins. Annu. Rev. Cell Dev. Biol. 19, 141–172 (2003).
Hoege, C., Pfander, B., Moldovan, G.-L., Pyrowolakis, G. & Jentsch, S. RAD6-dependent DNA repair is linked to modification of PCNA by ubiquitin and SUMO. Nature 419, 135–141 (2002).
Vibhuti, J. et al. A Decade of Boon or Burden: What Has the CHIP Ever Done for Cellular Protein Quality Control Mechanism Implicated in Neurodegeneration and Aging? Front. Mol. Neurosci. 9, 93 (2016).
Perrody, E. et al. Ubiquitin-dependent folding of the Wnt signaling coreceptor LRP6. Elife 5 (2016).
Mevissen, T. E. T. et al. Molecular basis of Lys11-polyubiquitin specificity in the deubiquitinase Cezanne. Nature 1–19; https://doi.org/10.1038/nature19836 (2016).
Garcia-Higuera, I. et al. Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway. Mol. Cell 7, 249–262 (2001).
Pronk, S. et al. GROMACS 4.5: a high-throughput and highly parallel open source molecular simulation toolkit. Bioinformatics 29, 845–854 (2013).
Hess, B., Kutzner, C., van der Spoel, D. & Lindahl, E. GROMACS 4: Algorithms for Highly Efficient, Load-Balanced, and Scalable Molecular Simulation. J. Chem. Theory Comput. 4, 435–47 (2008).
Van Der Spoel, D. et al. GROMACS: fast, flexible, and free. J. Comput. Chem. 26, 1701–18 (2005).
Sammalkorpi, M., Karttunen, M. & Haataja, M. Structural properties of ionic detergent aggregates: a large-scale molecular dynamics study of sodium dodecyl sulfate. J. Phys. Chem. B 111, 11722–33 (2007).
Malde, A. K. et al. An automated force field topology builder (ATB) and repository: Version 1.0. J Chem Theory Comput 7 (2011).
Schüttelkopf, A. W. & Van Aalten, D. M. F. PRODRG: A tool for high-throughput crystallography of protein-ligand complexes. Acta Crystallogr. Sect. D Biol. Crystallogr. 60, 1355–1363 (2004).
Berendsen, H. J. C., Grigera, J. R. & Straatsma, T. P. The Missing Term in Effective Pair Potentials. J. Phys. Chem. 91, 6269–6271 (1987).
Darden, T., York, D. & Pedersen, L. Particle mesh Ewald: An N-log(N) method for Ewald sums in large systems. J. Chem. Phys. 98, 10089 (1993).
Hoover Canonical dynamics: Equilibrium phase-space distributions. Phys. Rev. A, Gen. Phys. 31, 1695–1697 (1985).
Nosé, S. & Klein, M. Constant pressure molecular dynamics for molecular systems. Mol. Phys. 50, 1055–1076 (1983).
Parrinello, M. & Rahman, A. Polymorphic transitions in single crystals: A new molecular dynamics method. J. Appl. Phys. 52, 7182 (1981).
Kumari, R., Kumar, R., Lynn, A. & Lynn, A. g_mmpbsa —A GROMACS Tool for High-Throughput MM-PBSA Calculations. J. Chem. Inf. Model. 54, 1951–1962 (2014).
Baker, N. A., Sept, D., Joseph, S., Holst, M. J. & McCammon, J. A. Electrostatics of nanosystems: Application to microtubules and the ribosome. Proc. Natl. Acad. Sci. 98, 10037–10041 (2001).
Kollman, P. A. et al. Calculating structures and free energies of complex molecules: Combining molecular mechanics and continuum models. Acc. Chem. Res. 33, 889–897 (2000).
Ibarra-molero, B. et al. Thermal versus Guanidine-Induced Unfolding of Ubiquitin. An Analysis in Terms of the Contributions from Charge − Charge Interactions to Protein Stability Thermal versus Guanidine-Induced Unfolding of Ubiquitin. An Analysis in Terms of the Contributions. 8138–8149; https://doi.org/10.1021/bi9905819 (1999).
Khan, J. M. et al. Protonation favors aggregation of lysozyme with SDS. Soft Matter 10, 2591–2599 (2014).
Schneider, G. F., Shaw, B. F., Lee, A., Carillho, E. & Whitesides, G. M. Pathway for Unfolding of Ubiquitin in Sodium Dodecyl Sulfate, Studied by Capillary Electrophoresis Pathway for Unfolding of Ubiquitin in Sodium Dodecyl Sulfate, Studied by Capillary Electrophoresis. 17384–17393; https://doi.org/10.1021/ja804736t (2008).
Manning, M. & Colón, W. Structural basis of protein kinetic stability: Resistance to sodium dodecyl sulfate suggests a central role for rigidity and a bias toward β-sheet structure. Biochemistry 43, 11248–11254 (2004).
Khorasanizadeh, S., Peters, I. D. & Roder, H. Evidence for a three-state model of protein folding from kinetic analysis of ubiquitin variants with altered core residues. Nat. Struct. Biol. 3, 193–205 (1996).
Kumar, E. K. & Prabhu, N. P. Differential effects of ionic and non-ionic surfactants on lysozyme fibrillation. Phys. Chem. Chem. Phys. 16, 24076–24088 (2014).
Sinha, S. K., Chakraborty, S. & Bandyopadhyay, S. Thickness of the hydration layer of a protein from molecular dynamics simulation. J. Phys. Chem. B 112, 8203–8209 (2008).
Timasheff, S. N. Protein hydration, thermodynamic binding, and preferential hydration. Biochemistry 41, 13473–13482 (2002).
Acknowledgements
The authors would like to thank Reza Esmaeili, Samira Jahangiri, and Reza Rasoolzadeh for their assistance.
Author information
Authors and Affiliations
Contributions
F.M., S.M.A., F.R. and M.J. designed the research; F.M. and M.J. performed the MD simulations; M.J. analyzed the simulation data; F.M., F.R. and S.M.A. supervised and validated the project; M.J. and F.M. wrote the article and all authors approved the paper.
Corresponding author
Ethics declarations
Competing Interests
The authors declare that they have no competing interests.
Additional information
Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Electronic supplementary material
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Jafari, M., Mehrnejad, F., Rahimi, F. et al. The Molecular Basis of the Sodium Dodecyl Sulfate Effect on Human Ubiquitin Structure: A Molecular Dynamics Simulation Study. Sci Rep 8, 2150 (2018). https://doi.org/10.1038/s41598-018-20669-7
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-018-20669-7
- Springer Nature Limited
This article is cited by
-
Molecular dynamics simulation of the effect of temperature on the conformation of ubiquitin protein
Journal of Molecular Modeling (2024)
-
Evaluating and optimizing Acid-pH and Direct Lysis RNA extraction for SARS-CoV-2 RNA detection in whole saliva
Scientific Reports (2024)
-
Structure based innovative approach to analyze aptaprobe–GPC3 complexes in hepatocellular carcinoma
Journal of Nanobiotechnology (2022)
-
Assessment of viability in coral oocytes: a biochemical approach to achieve reliable assays
Marine Biology (2022)
-
Optimizing Decellularization Strategies for the Efficient Production of Whole Rat Kidney Scaffolds
Tissue Engineering and Regenerative Medicine (2021)