Frustration in biomolecules

被引:232
作者
Ferreiro, Diego U. [1 ]
Komives, Elizabeth A. [2 ]
Wolynes, Peter G. [3 ,4 ]
机构
[1] Univ Buenos Aires, Fac Ciencias Exactas & Nat, CONICET IQUIBICEN, Dept Quim Biol,Prot Physiol Lab, Buenos Aires, DF, Argentina
[2] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
[3] Rice Univ, Dept Chem, Dept Phys, Houston, TX 77005 USA
[4] Rice Univ, Ctr Theoret Biol Phys, Houston, TX 77005 USA
基金
美国国家科学基金会;
关键词
ANKYRIN REPEAT PROTEINS; TERTIARY STRUCTURE RECOGNITION; FACILITATED TARGET LOCATION; TRANSITION-STATE ENSEMBLE; ENERGY LANDSCAPE MODEL; FOLDING KINETICS; STATISTICAL-MECHANICS; DNA BINDING; NONNATIVE INTERACTIONS; ASSOCIATION PROPERTIES;
D O I
10.1017/S0033583514000092
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Biomolecules are the prime information processing elements of living matter. Most of these inanimate systems are polymers that compute their own structures and dynamics using as input seemingly random character strings of their sequence, following which they coalesce and perform integrated cellular functions. In large computational systems with finite interaction-codes, the appearance of conflicting goals is inevitable. Simple conflicting forces can lead to quite complex structures and behaviors, leading to the concept of frustration in condensed matter. We present here some basic ideas about frustration in biomolecules and how the frustration concept leads to a better appreciation of many aspects of the architecture of biomolecules, and especially how biomolecular structure connects to function by means of localized frustration. These ideas are simultaneously both seductively simple and perilously subtle to grasp completely. The energy landscape theory of protein folding provides a framework for quantifying frustration in large systems and has been implemented at many levels of description. We first review the notion of frustration from the areas of abstract logic and its uses in simple condensed matter systems. We discuss then how the frustration concept applies specifically to heteropolymers, testing folding landscape theory in computer simulations of protein models and in experimentally accessible systems. Studying the aspects of frustration averaged over many proteins provides ways to infer energy functions useful for reliable structure prediction. We discuss how frustration affects folding mechanisms. We review here how the biological functions of proteins are related to subtle local physical frustration effects and how frustration influences the appearance of metastable states, the nature of binding processes, catalysis and allosteric transitions. In this review, we also emphasize that frustration, far from being always a bad thing, is an essential feature of biomolecules that allows dynamics to be harnessed for function. In this way, we hope to illustrate how Frustration is a fundamental concept in
引用
收藏
页码:285 / 363
页数:79
相关论文
共 243 条
[1]   STRUCTURE OF RHOMBOHEDRAL 2 ZINC INSULIN CRYSTALS [J].
ADAMS, MJ ;
BLUNDELL, TL ;
DODSON, EJ ;
DODSON, GG ;
VIJAYAN, M ;
BAKER, EN ;
HARDING, MM ;
HODGKIN, DC ;
RIMMER, B ;
SHEAT, S .
NATURE, 1969, 224 (5218) :491-&
[2]   ANALYSIS OF REPEAT-PROTEIN FOLDING USING NEAREST-NEIGHBOR STATISTICAL MECHANICAL MODELS [J].
Aksel, Tura ;
Barrick, Doug .
METHODS IN ENZYMOLOGY: BIOTHERMODYNAMICS,VOL 455, PART A, 2009, 455 :95-125
[3]   ANTIFERROMAGNETISM - THEORY OF SUPEREXCHANGE INTERACTION [J].
ANDERSON, PW .
PHYSICAL REVIEW, 1950, 79 (02) :350-356
[4]   Emergence of symmetry in homooligomeric biological assemblies [J].
Andre, Ingemar ;
Strauss, Charlie E. M. ;
Kaplan, David B. ;
Bradley, Philip ;
Baker, David .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (42) :16148-16152
[5]   PRINCIPLES THAT GOVERN FOLDING OF PROTEIN CHAINS [J].
ANFINSEN, CB .
SCIENCE, 1973, 181 (4096) :223-230
[6]  
[Anonymous], 2005, L'individuation a la lumiere des notions de forme et d'information
[7]   THE STRUCTURE OF 2ZN PIG INSULIN CRYSTALS AT 1.5-A RESOLUTION [J].
BAKER, EN ;
BLUNDELL, TL ;
CUTFIELD, JF ;
CUTFIELD, SM ;
DODSON, EJ ;
DODSON, GG ;
HODGKIN, DMC ;
HUBBARD, RE ;
ISAACS, NW ;
REYNOLDS, CD ;
SAKABE, K ;
SAKABE, N ;
VIJAYAN, NM .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1988, 319 (1195) :369-&
[8]   Folding landscapes of ankyrin repeat proteins: experiments meet theory [J].
Barrick, Doug ;
Ferreiro, Diego U. ;
Komives, Elizabeth A. .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2008, 18 (01) :27-34
[9]   Protein design: The choice of de novo sequences [J].
Beasley, JR ;
Hecht, MH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (04) :2031-2034
[10]   The Protein Data Bank [J].
Berman, HM ;
Westbrook, J ;
Feng, Z ;
Gilliland, G ;
Bhat, TN ;
Weissig, H ;
Shindyalov, IN ;
Bourne, PE .
NUCLEIC ACIDS RESEARCH, 2000, 28 (01) :235-242