...
首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Sequence, structure, and cooperativity in folding of elementary protein structural motifs
【24h】

Sequence, structure, and cooperativity in folding of elementary protein structural motifs

机译:Sequence, structure, and cooperativity in folding of elementary protein structural motifs

获取原文
获取原文并翻译 | 示例
           

摘要

Residue-level unfolding of two helix-turn-helix proteins-one naturally occurring and one de novo designed-is reconstructed from multiple sets of site-specific C-13 isotopically edited infrared (IR) and circular dichroism (CD) data using Ising-like statistical-mechanical models. Several model variants are parameterized to test the importance of sequence-specific interactions (approximated by Miyazawa-Jernigan statistical potentials), local structural flexibility (derived from the ensemble of NMR structures), interhelical hydrogen bonds, and native contacts separated by intervening disordered regions (through the Wako-Saito-Munoz-Eaton scheme, which disallows such configurations). The models are optimized by directly simulating experimental observables: CD ellipticity at 222 nm for model proteins and their fragments and C-13-amide I bands for multiple isotopologues of each protein. We find that data can be quantitatively reproduced by the model that allows two interacting segments flanking a disordered loop (double sequence approximation) and incorporates flexibility in the native contact maps, but neither sequence-specific interactions nor hydrogen bonds are required. The near-identical free energy profiles as a function of the global order parameter are consistent with expected similar folding kinetics for nearly identical structures. However, the predicted folding mechanism for the two motifs is different, reflecting the order of local stability. We introduce free energy profiles for "experimental" reaction coordinates-namely, the degree of local folding as sensed by site-specific C-13-edited IR, which highlight folding heterogeneity and contrast its overall, average description with the detailed, local picture.

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号