The Limited Role of Nonnative Contacts in the Folding Pathways of a Lattice Protein

被引:37
作者
Gin, Brian C. [1 ,2 ,3 ]
Garrahan, Juan P. [4 ]
Geissler, Phillip L. [1 ,2 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Lawrence Berkeley Lab, Chem Sci & Phys Biosci Div, Berkeley, CA 94720 USA
[3] Univ Calif San Francisco, Sch Med, San Francisco, CA 94143 USA
[4] Univ Nottingham, Sch Phys & Astron, Nottingham NG7 2RD, England
基金
英国工程与自然科学研究理事会;
关键词
Go model; nonnative contacts; lattice model; protein folding; principle of minimum frustration; ENERGY LANDSCAPE; TRANSITION-STATE; MODEL; MECHANISMS; KINETICS; THERMODYNAMICS; SIMULATION; SEQUENCES; DYNAMICS; EVOLUTION;
D O I
10.1016/j.jmb.2009.06.058
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Models of protein energetics that neglect interactions between amino acids that are not adjacent in the native state, such as the Go model, encode or underlie many influential ideas on protein folding. Implicit in this simplification is a crucial assumption that has never been critically evaluated in a broad context: Detailed mechanisms of protein folding are not biased by normative contacts, typically argued to be a consequence of sequence design and/or topology. Here we present, using computer simulations of a well-studied lattice heteropolymer model, the first systematic test of this oft-assumed correspondence over the statistically significant range of hundreds of thousands of amino acid sequences that fold to the same native structure. Contrary to previous conjectures, we find a multiplicity of folding mechanisms, suggesting that Go-like models cannot be justified by considerations of topology alone. Instead, we find that the crucial factor in discriminating among topological pathways is the heterogeneity of native contact energies: The order in which native contacts accumulate is profoundly insensitive to omission of nonnative interactions, provided that native contact heterogeneity is retained. This robustness holds over a surprisingly wide range of folding rates for our designed sequences. Mirroring predictions based on the principle of minimum frustration, fast-folding sequences match their Go-like counterparts in both topological mechanism and transit times. Less optimized sequences dwell much longer in the unfolded state and/or off-pathway intermediates than do Go-like models. For dynamics that bridge unfolded and unfolded states, however, even slow folders exhibit topological mechanisms and transit times nearly identical with those of their Go-like counterparts. Our results do not imply a direct correspondence between folding trajectories of Go-like models and those of real proteins, but they do help to clarify key topological and energetic assumptions that are commonly used to justify such caricatures. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1303 / 1314
页数:12
相关论文
共 41 条
[1]   SPECIFIC NUCLEUS AS THE TRANSITION-STATE FOR PROTEIN-FOLDING - EVIDENCE FROM THE LATTICE MODEL [J].
ABKEVICH, VI ;
GUTIN, AM ;
SHAKHNOVICH, EI .
BIOCHEMISTRY, 1994, 33 (33) :10026-10036
[2]   SPIN-GLASSES AND THE STATISTICAL-MECHANICS OF PROTEIN FOLDING [J].
BRYNGELSON, JD ;
WOLYNES, PG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (21) :7524-7528
[3]   The effects of nonnative interactions on protein folding rates: Theory and simulation [J].
Clementi, C ;
Plotkin, SS .
PROTEIN SCIENCE, 2004, 13 (07) :1750-1766
[4]   Identifying the protein folding nucleus using molecular dynamics [J].
Dokholyan, NV ;
Buldyrev, SV ;
Stanley, HE ;
Shakhnovich, EI .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 296 (05) :1183-1188
[5]   On the transition coordinate for protein folding [J].
Du, R ;
Pande, VS ;
Grosberg, AY ;
Tanaka, T ;
Shakhnovich, ES .
JOURNAL OF CHEMICAL PHYSICS, 1998, 108 (01) :334-350
[6]   Identifying critical residues in protein folding:: Insights from φ-value and Pfold analysis [J].
Faisca, P. F. N. ;
Travasso, R. D. M. ;
Ball, R. C. ;
Shakhnovich, E. I. .
JOURNAL OF CHEMICAL PHYSICS, 2008, 129 (09)
[7]  
Fischer K.H., 1993, Spin glasses
[8]   THEORETICAL-STUDIES OF PROTEIN FOLDING [J].
GO, N .
ANNUAL REVIEW OF BIOPHYSICS AND BIOENGINEERING, 1983, 12 :183-210
[9]   Temperature dependence of the folding rate in a simple protein model: Search for a "glass" transition [J].
Gutin, A ;
Sali, A ;
Abkevich, V ;
Karplus, M ;
Shakhnovich, EI .
JOURNAL OF CHEMICAL PHYSICS, 1998, 108 (15) :6466-6483
[10]   Coevolution of Function and the Folding Landscape: Correlation with Density of Native Contacts [J].
Hills, Ronald D., Jr. ;
Brooks, Charles L., III .
BIOPHYSICAL JOURNAL, 2008, 95 (09) :L57-L59