- Methodology article
- Open Access
Stereochemical errors and their implications for molecular dynamics simulations
© Schreiner et al; licensee BioMed Central Ltd. 2011
- Received: 18 January 2011
- Accepted: 23 May 2011
- Published: 23 May 2011
Biological molecules are often asymmetric with respect to stereochemistry, and correct stereochemistry is essential to their function. Molecular dynamics simulations of biomolecules have increasingly become an integral part of biophysical research. However, stereochemical errors in biomolecular structures can have a dramatic impact on the results of simulations.
Here we illustrate the effects that chirality and peptide bond configuration flips may have on the secondary structure of proteins throughout a simulation. We also analyze the most common sources of stereochemical errors in biomolecular structures and present software tools to identify, correct, and prevent stereochemical errors in molecular dynamics simulations of biomolecules.
Use of the tools presented here should become a standard step in the preparation of biomolecular simulations and in the generation of predicted structural models for proteins and nucleic acids.
- Molecular Dynamic Simulation
- Peptide Bond
- Chiral Center
- Alternative Conformation
- Stereochemical Configuration
Another type of asymmetry is encountered in the conformation of the peptide bond connecting the carboxy end of one amino acid to the amino end of the next one in a peptide or protein. Due to the partial double-bond character of the C n -Nn+1bond, the atoms Cα, n, C n , On, Cα, n+1, Nn+1and its hydrogen are in a plane (see, however, Ref ) and the rotation around the C n -Nn+1bond is restricted by a barrier of about 20 kcal/mol [10, 11]. Depending on the value of the dihedral angle ω described by Cα, n, C n , Nn+1and Cα, n+1, one can distinguish cis (ω ≈ 0°) and trans (ω ≈ 180°) isomers  (see Figure 1C). For sterical reasons, the trans isomer is energetically more stable and, thus, is the prevalent form in proteins. Additionally, the rather high rotational barrier makes the interconversion of the two isomers a very slow process at room temperature. Nevertheless, cis peptide bonds can be found in nature [13, 14]. The vast majority of cis bonds are observed before a proline residue, Xaa-Pro, with Xaa being any amino acid. The formation of these cis peptides is catalyzed by special enzymes, prolyl-cis/trans isomerases [15, 16]. Prolyl-cis/trans isomerization is an important molecular switch  and the occurrence of enzymes specialized for this particular isomerization underpins its biological significance. Non-prolyl cis peptide bonds can also be found in proteins, but much less frequently than Xaa-Pro [13, 14] and only one protein, DnaK, is known to promote peptide isomerization of non-prolyl peptide bonds . In particular, DnaK was found to accelerate the isomerization of Ala-Xaa bonds, Xaa being Ala, Gly, Glu, Ile, Leu, Lys, Met, or Ser. Metal ions can also play a role both in stabilizing the cis isomer and in promoting isomerization [19–22].
Correct stereochemistry of a structural model is important for its interpretation and critical if the model is to be subject to a molecular dynamics simulation. Force fields typically employed in biomolecular simulations do not contain terms to enforce stereochemistry and support either enantiomer or peptide isomer. Errors in the input structure usually persist throughout the simulation and, as will be shown below, can propagate and lead to severe artifacts. Even in cases where stereochemical errors do not lead to such large-scale problems, such errors must be avoided since they represent deviations of the simulated system from the biological reality that is to be modeled. There is a steady trend in the field of biomolecular simulations toward the study of large biomolecular assemblies and the usage of models based on structure prediction. Our recent experience [23–25] shows that stereochemical errors often arise in the preparation of large systems for simulation, particularly when some components must be modeled prior to simulation.
A variety of servers and programs are available for structure validation, a vital stage in the preparation of files for deposition in a coordinate database. One example is the SAVES server , which provides an interface to tools such as PROCHECK , WHAT_CHECK , and other programs to detect irregularities in geometry and structure such as chirality, bond angles, close contacts, or rotamer states of amino acid side chains. Other examples with similar functionality include the MolProbity  server as well as the PDB validation service .
All of the aforementioned tools for structure validation are primarily designed to validate experimentally obtained models and not to ensure proper stereochemistry in simulations. Additionally, although irregularities are reported, none of the tools we are aware of allow the user to inspect and correct stereochemical errors easily and immediately. We have thus written software tools to help researchers easily detect, correct, and avoid stereochemical errors in simulations.
In the following, we start by illustrating how errors in chirality and peptide bond configuration can affect secondary structure of proteins in molecular dynamics simulations. We then present software tools to identify, visually inspect, and interactively correct stereochemical errors in structural models of proteins and nucleic acids. Next, we discuss the most common sources of stereochemical errors in simulations, alongside a systematic analysis of the entire Protein Data Bank . Finally, we provide a recommended workflow to avoid stereochemical errors in biomolecular simulations.
Consequences of stereochemical errors in biomolecular simulations
As demonstrated above, the impact of errors in chirality or peptide bond isomerization on secondary structure can be dramatic. Note, however, that the chosen example represents the worst case scenario in terms of severity of the structural disturbance - in a real protein, tertiary interactions may provide stabilization of the native structure and, thus, dampen the effect or extend the time scale on which the structural disturbance becomes apparent.
Tools to identify, inspect, and correct stereochemical errors
Having demonstrated the impact of stereochemical errors on structure, the question of how to ensure stereochemical correctness in simulation naturally arises. In general, biological systems can contain amino acids or sugars of different chirality, as well as both peptide isomers. Thus, an automatic procedure to "correct" the structure is not appropriate unless one is absolutely certain that only one enantiomer and isomer occurs. Therefore, we designed a semi-automatic four-step protocol to correct errors and to ensure stereochemical integrity of a simulated system. For both chirality and peptide bond conformation, the protocol was implemented into easy-to-use plugins for the molecular visualization and analysis program VMD , referred to as Chirality and Cispeptide plugins, respectively. The plugins make use of the molecular dynamics simulation package NAMD  in the correction step. Both software packages are open source and freely available. The current implementation provides both a graphical and a command-line user interface. Use of each plugin follows a similar 4-step process, namely: (1) identify stereochemical anomalies; (2) visually inspect each anomaly and decide if it should be corrected; (3) move selected atoms as to change the stereochemical configuration; and (4) locally optimize the structure. In the following, we describe the four steps using the Cispeptide plugin as an example. Full documentation is available on the VMD website . An additional step-by-step practical guide can be found in a tutorial describing both plugins .
Sources of stereochemical errors
Most molecular dynamics simulations of single proteins are relatively safe from stereochemical errors, given that molecular structures are validated upon deposition into the PDB. The irregularities detected in the validation step are usually either corrected or reported in the header of the PDB file. Using a structure from the PDB for simulations, together with a careful examination of the file header, usually means that the stereochemical integrity of the simulation is secure (barring special cases discussed below), because during an equilibrium simulation the force field will preserve stereochemistry. However, since force fields used for molecular dynamics simulations support both types of chirality as well as both peptide bond isomers, an existing error will persist throughout the simulation.
Chirality errors and cis peptide bonds in the Protein Data Bank
Cis peptide bonds
Residues per error 3
Structures analyzed 4
Structures with errors
Residues per cis bond 3
Structures analyzed 4
Structures with cis bonds
In a subset of structures, chirality errors (153 structures) and cis peptide bonds (62 structures) were reported in the PDB file, but were not detected by the plugins. To understand the discrepancies, about half of the structures in each subset was visually inspected. In the case of cis peptides, the differences were due to missing atoms in the deposited model, errors being present in only one alternative conformation or model (see Methods), pathologically distorted structures, and, most frequently, incorrect entries in the PDB header. Similarly, the reasons for the discrepancies in chirality were that errors occurred in cofactors not checked by the plugin, the anomalies were present in only one alternative conformation or model (see Methods), or the annotations in the PDB header were incorrect.
The plugins also identified many structures with stereochemical anomalies not reported in the PDB header. According to the current PDB format standard, each cis peptide bond should be reported in a separate CISPEP record. It is then possible to compare each identified cis peptide bond with the PDB header. There were in total 2,518 cis peptide bonds identified by the Cispeptide plugin but not reported in the PDB files. Visual inspection of 20 such files did not reveal any incorrect identification by the plugin. Chirality issues should be reported in CAVEAT records of the PDB header. Unfortunately, since CAVEAT records are free format, rarely are chirality errors individually reported. Furthermore, many PDB structures have chiral errors inconsistently documented in REMARK 500 records instead. Thus, a similar comparison on a per-error basis cannot be performed for the Chirality plugin; instead, we can only report that 348 PDB files contain chirality anomalies according to the Chirality plugin, but lack the corresponding annotation in their PDB headers. Upon visual inspection of 20 files, the structures fell into two categories: either there should be a D-amino acid (non-ribosomal peptides) or the PDB header is simply missing the required annotation.
Apart from errors already present in experimentally determined structures, our experience shows that there are three main sources of stereochemical errors in simulations. The first source is found in modeling steps, particularly homology modeling: any regions of a structure that were modeled de novo, especially at the junctions of the known and modeled part of a protein, are prone to peptide isomerization errors. The second common source is found in the setup protocol for a simulation. This includes the preparation of the system and its initial relaxation. In particular, sterical clashes between atoms can lead to errors in chirality and isomerization state of peptide bonds. Again, such behavior is particularly likely at the interface between known and modeled portions of a structure, which may contain severe distortions prior to equilibration. Although the barriers for isomerization or a flip in chirality are large enough to prevent these events in an equilibrium simulation at physiological temperatures (e.g., 21 kcal/mol in CHARMM22 ), forces arising during the initial structure optimization, necessary to relax possible clashes, may be large enough to introduce errors into the structure. This source of errors becomes increasingly important as the field of computational biophysics moves towards multi-component assemblies, the structures of which are often modeled based on high-resolution models of their constituents and low-resolution data of the whole complex. Finally, errors can also be introduced during structure optimizations if additional forces are applied on the system. Of particular interest at this point is the molecular dynamics flexible fitting (MDFF) method , which flexibly fits atomic-resolution structures into low-resolution density maps. In some (rare) cases, it was observed that forces arising from the MDFF method during initial structure optimization were large enough to cause stereochemical errors. System setup protocols where the system is simulated at very high temperatures (e.g., to obtain heat-denatured structures) may also allow incorrect isomerization events.
The Chirality and Cispeptide plugins can be used to generate harmonic restraints designed to preserve the current isomerization state of each chiral center and peptide bond. The restraints can be used in simulations with NAMD, effectively preventing stereochemical errors from arising during simulation. These restraints should be removed prior to production equilibrium simulations, since they are not required and would represent an unnecessary modification of the force field employed.
Build system for MD simulation (model missing components, assemble structure, embed system in a water box, and add counterions).
Check stereochemistry with the Chirality and Cispeptide plugins, correcting errors if applicable. Repeat until no further errors are detected. Make sure that the detected irregularities are indeed errors and not naturally occurring.
Proceed to production simulation.
For simulations in which large forces are expected (e.g., flexible fitting with the MDFF method  or temperature-induced denaturation), it is recommended that, in addition to the workflow above, harmonic restraints generated by the Chirality and Cispeptide plugins are applied throughout the simulation.
The simulations presented here illustrate the drastic effects that stereochemical errors can have in biomolecular simulations. Experimentally determined structures may contain stereochemical errors, and various modeling approaches can further increase the number of such errors. As the community moves toward simulation of large, multi-component complexes and uses to an increasing extent models based on structure prediction, the issue of stereochemical correctness becomes even more relevant. We thus developed tools to identify, inspect, and correct stereochemical errors in protein and nucleic acid structures. In particular, chirality and the isomerization state of a peptide bond are examined. The main advantage of the offered tools is the possibility to immediately inspect and correct the detected errors. The tools are implemented as plugins to the molecular visualization and analysis program VMD. The recommended workflow presented above effectively avoids artifacts in simulations due to stereochemical errors. We hope that checks for stereochemical correctness become a standard step of any biomolecular simulation or generation of predicted structural models for proteins and nucleic acids.
Project name: cispeptide, chirality; included into VMD
Project home page: http://www.ks.uiuc.edu/Research/vmd
Operating system(s): Platform independent
Programming language: Tcl
Other requirements: VMD 1.9 or higher, for molecular dynamics part: NAMD 2.7 or higher
License: UIUC Open Source License http://www.ks.uiuc.edu/Research/vmd/plugins/pluginlicense.htmlhttp://www.ks.uiuc.edu/Research/namd/license.html
Molecular dynamics simulations
Molecular dynamics simulations were conducted using NAMD 2.7 . The system consisted of the 15-amino-acid-long α-helix AAQAAAAQAAAAQAA solvated in TIP3P water. The N- and C-terminus were acetylated and amidated, respectively. The system was set up in VMD . In particular, the helix was constructed using the molefacture plugin, after which the full system was built with the solvate and psfgen plugins.
All simulations were performed in the NpT ensemble (T = 310 K, p = 1 atm). The stereochemically correct system was equilibrated using a 2-step protocol. First, water and side chains were equilibrated for 400 ps while the backbone of the peptide was restrained, after which all restraints were removed and the system was equilibrated for an additional 3.6 ns. The resulting structure was used to manually introduce a chirality flip at Gln8 and to isomerize the peptide bond between Gln8 and Ala9 into the cis form (see Figure 2). Starting from the three obtained systems, the simulations were continued for 32 ns in each case. The equations of motion were integrated using periodic boundary conditions and a 2-fs time step, with bonded interactions calculated every 2 fs. Nonbonded, short-range interactions were calculated every 4 fs using a distance cut-off of 10 Å with a switching function applied at 9 Å. Long-range electrostatic interactions were updated every 6 fs using the Particle Mesh Ewald (PME) method and the PME grid density was never less than 1/Å3. The simulations presented here were performed with the CHARMM27 force field [39, 41] with the CMAP correction .
Analysis of the PDB
Each structure available in the PDB as of mid-September 2010 was analyzed using the Chirality and Cispeptide VMD plugins. In case of multiple models (typically in structures solved by NMR), only the first model was considered in the analysis. When multiple alternative conformations of certain residues were present, as indicated by the altLoc field in the PDB file, only the first conformation was considered. For comparison and validation purposes, each PDB file header was parsed for reported cis peptide bonds (CISPEP records) and unusual chirality configurations (CAVEAT and REMARK 500 records).
This work was supported by the National Institutes of Health (P41-RR005969) and the National Science Foundation (PHY0822613). E.S. and L.G.T. were supported by fellowships from the Humboldt Foundation and the European Molecular Biology Organization, respectively.
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