Simple and versatile restraints for the accurate modeling of α-helical coiled-coil structures of multiple strandedness, orientation and composition

• Published in: Biopolymers Vol. 81; no. 3; pp. 202 - 214
• Main Authors: Charest, Gabriel, Lavigne, Pierre
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 15-02-2006
• Subjects: Amino Acid Sequence; Biopolymers - chemistry; coiled coils; leucine zippers; modeling; Models, Molecular; Molecular Sequence Data; Protein Conformation; Protein Structure, Secondary; protein-protein interactions; SNARE Proteins - chemistry; structure
• ISSN: 0006-3525; 1097-0282
• DOI: 10.1002/bip.20401

We present a minimalist approach for the modeling of the three‐dimensional structure of multistranded α‐helical coiled coils. The approach is based on empirical principles introduced by F. H. C. Crick (F. H. C. Crick, Acta Crystallogr, 1953, Vol. 6, pp. 689–697). Crick hypothesized that keeping the distance between the residues at the interacting interface of α‐helices constant would lead to supercoiling or the formation of a coiled coil through the knobs‐into‐holes mode of packing. We have implemented the latter hypothesis in a simulating annealing protocol in the simple form of interhelical distance restraints (two per heptad) between Cα at the interfacial positions a and d. To demonstrate the authenticity of Crick's hypothesis and the precision and accuracy of our approach, we have modeled the crystal structures of six synthetic coiled coils in dimeric, trimeric, and tetrameric states. The mean root mean square deviations (RMSDs) between the backbone atoms of the ensemble of structures calculated and those of the corresponding geometric averages is always below 0.76 Å, indicating that our protocol has an excellent degree of convergence and precision. The RMSDs between the backbone atoms of each of the six geometric average structures and the backbone of the corresponding crystal structures all range between 0.43 and 0.95 Å, indicative of excellent accuracy and proving the authenticity of Crick's hypothesis. Moreover, without specifying any dihedral angles, we found that in 81% of the occurrences, the most populated conformer of the side chains at positions a and d in the ensembles calculated were identical to those observed in the crystal structures. This shows that our simple approach, which is the simplest reported so far, can generate accurate results for the backbone and side chains. Finally, as a test case for a wider application of our approach in the field of structural proteomics, we describe the successful modeling of the overall structure of SNARE and the organization of its interfacial ionic layer known to play an important functional role. © 2005 Wiley Periodicals, Inc. Biopolymers 81: 202–214, 2006
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