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Accounting for a mirror-image conformation as a subtle effect in protein folding.


ABSTRACT: By using local (free-energy profiles along the amino acid sequence and (13)C(?) chemical shifts) and global (principal component) analyses to examine the molecular dynamics of protein-folding trajectories, generated with the coarse-grained united-residue force field, for the B domain of staphylococcal protein A, we are able to (i) provide the main reason for formation of the mirror-image conformation of this protein, namely, a slow formation of the second loop and part of the third helix (Asp29-Asn35), caused by the presence of multiple local conformational states in this portion of the protein; (ii) show that formation of the mirror-image topology is a subtle effect resulting from local interactions; (iii) provide a mechanism for how protein A overcomes the barrier between the metastable mirror-image state and the native state; and (iv) offer a plausible reason to explain why protein A does not remain in the metastable mirror-image state even though the mirror-image and native conformations are at least energetically compatible.

SUBMITTER: Kachlishvili K 

PROVIDER: S-EPMC4060689 | biostudies-literature | 2014 Jun

REPOSITORIES: biostudies-literature

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Accounting for a mirror-image conformation as a subtle effect in protein folding.

Kachlishvili Khatuna K   Maisuradze Gia G GG   Martin Osvaldo A OA   Liwo Adam A   Vila Jorge A JA   Scheraga Harold A HA  

Proceedings of the National Academy of Sciences of the United States of America 20140527 23


By using local (free-energy profiles along the amino acid sequence and (13)C(α) chemical shifts) and global (principal component) analyses to examine the molecular dynamics of protein-folding trajectories, generated with the coarse-grained united-residue force field, for the B domain of staphylococcal protein A, we are able to (i) provide the main reason for formation of the mirror-image conformation of this protein, namely, a slow formation of the second loop and part of the third helix (Asp29-  ...[more]

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