Pathways and intermediates in forced unfolding of spectrin repeats

被引:64
作者
Altmann, SM
Grünberg, RG
Lenne, PF
Ylänne, J
Raae, A
Herbert, K
Saraste, M
Nilges, M
Hörber, JKH
机构
[1] European Mol Biol Lab, Cell Biol & Biophys Program, D-69117 Heidelberg, Germany
[2] Inst Pasteur, Unite Bioinformat Struct, F-75015 Paris, France
[3] Domaine Univ St Jerome, ENSPM, Inst Fresnel, F-13397 Marseille 20, France
[4] Univ Oulu, FIN-90570 Oulu, Finland
[5] Bioctr Oulu, Dept Biochem, FIN-90570 Oulu, Finland
[6] Univ Bergen, Dept Biol Mol, HIB, N-5020 Bergen, Norway
[7] European Mol Biol Lab, Struct & Computat Biol Program, D-69117 Heidelberg, Germany
基金
芬兰科学院;
关键词
atomic force microscopy; molecular dynamics simulation; spectrin; unfolding intermediate; elasticity;
D O I
10.1016/S0969-2126(02)00808-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Spectrin repeats are triple-helical coiled-coil domains found in many proteins that are regularly subjected to mechanical stress. We used atomic force microscopy technique and steered molecular dynamics simulations to study the behavior of a wild-type spectrin repeat and two mutants. The experiments indicate that spectrin repeats can form stable unfolding intermediates when subjected to external forces. In the simulations the unfolding proceeded via a variety of pathways. Stable intermediates were associated to kinking of the central helix close to a proline residue. A mutant stabilizing the central helix showed no intermediates in experiments, in agreement with simulation. Spectrin repeats may thus function as elastic elements, extendable to intermediate states at various lengths.
引用
收藏
页码:1085 / 1096
页数:12
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