Literature DB >> 20932976

Probing designability via a generalized model of helical bundle geometry.

Gevorg Grigoryan1, William F Degrado.   

Abstract

Because the space of folded protein structures is highly degenerate, with recurring secondary and tertiary motifs, methods for representing protein structure in terms of collective physically relevant coordinates are of great interest. By collapsing structural diversity to a handful of parameters, such methods can be used to delineate the space of designable structures (i.e., conformations that can be stabilized with a large number of sequences)-a crucial task for de novo protein design. We first demonstrate this on natural α-helical coiled coils using the Crick parameterization. We show that over 95% of known coiled-coil structures are within  1-Å C(α) root mean square deviation of a Crick-ideal backbone. Derived parameters show that natural geometric space of coiled coils is highly restricted and can be represented by "allowed" conformations amidst a potential continuum of conformers. Allowed structures have (1) restricted axial offsets between helices, which differ starkly between parallel and anti-parallel structures; (2) preferred superhelical radii, which depend linearly on the oligomerization state; (3) pronounced radius-dependent a- and d-position amino acid propensities; and (4) discrete angles of rotation of helices about their axes, which are surprisingly independent of oligomerization state or orientation. In all, we estimate the space of designable coiled-coil structures to be reduced at least 160-fold relative to the space of geometrically feasible structures. To extend the benefits of structural parameterization to other systems, we developed a general mathematical framework for parameterizing arbitrary helical structures, which reduces to the Crick parameterization as a special case. The method is successfully validated on a set of non-coiled-coil helical bundles, frequent in channels and transporter proteins, which show significant helix bending but not supercoiling. Programs for coiled-coil parameter fitting and structure generation are provided via a web interface at http://www.gevorggrigoryan.com/cccp/, and code for generalized helical parameterization is available upon request. Copyright Â
© 2010 Elsevier Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20932976      PMCID: PMC3052747          DOI: 10.1016/j.jmb.2010.08.058

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  57 in total

1.  Socket: a program for identifying and analysing coiled-coil motifs within protein structures.

Authors:  J Walshaw; D N Woolfson
Journal:  J Mol Biol       Date:  2001-04-13       Impact factor: 5.469

2.  Statistical theory of combinatorial libraries of folding proteins: energetic discrimination of a target structure.

Authors:  J Zou; J G Saven
Journal:  J Mol Biol       Date:  2000-02-11       Impact factor: 5.469

3.  Protein topology and stability define the space of allowed sequences.

Authors:  Patrice Koehl; Michael Levitt
Journal:  Proc Natl Acad Sci U S A       Date:  2002-01-22       Impact factor: 11.205

4.  D(n)-symmetrical tertiary templates for the design of tubular proteins.

Authors:  B North; C M Summa; G Ghirlanda; W F DeGrado
Journal:  J Mol Biol       Date:  2001-08-31       Impact factor: 5.469

5.  Side-chain repacking calculations for predicting structures and stabilities of heterodimeric coiled coils.

Authors:  A E Keating; V N Malashkevich; B Tidor; P S Kim
Journal:  Proc Natl Acad Sci U S A       Date:  2001-12-18       Impact factor: 11.205

6.  The designability of protein structures.

Authors:  R Helling; H Li; R Mélin; J Miller; N Wingreen; C Zeng; C Tang
Journal:  J Mol Graph Model       Date:  2001       Impact factor: 2.518

7.  Crystal structure of a naturally occurring parallel right-handed coiled coil tetramer.

Authors:  J Stetefeld; M Jenny; T Schulthess; R Landwehr; J Engel; R A Kammerer
Journal:  Nat Struct Biol       Date:  2000-09

8.  Native protein sequences are close to optimal for their structures.

Authors:  B Kuhlman; D Baker
Journal:  Proc Natl Acad Sci U S A       Date:  2000-09-12       Impact factor: 11.205

9.  Generalized Crick equations for modeling noncanonical coiled coils.

Authors:  Gerald Offer; Matthew R Hicks; Derek N Woolfson
Journal:  J Struct Biol       Date:  2002 Jan-Feb       Impact factor: 2.867

Review 10.  The gates of ion channels and enzymes.

Authors:  Huan-Xiang Zhou; J Andrew McCammon
Journal:  Trends Biochem Sci       Date:  2009-11-18       Impact factor: 13.807

View more
  81 in total

Review 1.  Computational protein design: engineering molecular diversity, nonnatural enzymes, nonbiological cofactor complexes, and membrane proteins.

Authors:  Jeffery G Saven
Journal:  Curr Opin Chem Biol       Date:  2011-04-12       Impact factor: 8.822

2.  Artificial Diiron Enzymes with a De Novo Designed Four-Helix Bundle Structure.

Authors:  Marco Chino; Ornella Maglio; Flavia Nastri; Vincenzo Pavone; William F DeGrado; Angela Lombardi
Journal:  Eur J Inorg Chem       Date:  2015-07-06       Impact factor: 2.524

3.  Competition between Coiled-Coil Structures and the Impact on Myosin-10 Bundle Selection.

Authors:  Kevin C Vavra; Youlin Xia; Ronald S Rock
Journal:  Biophys J       Date:  2016-06-07       Impact factor: 4.033

4.  Programmable design of orthogonal protein heterodimers.

Authors:  Zibo Chen; Scott E Boyken; Mengxuan Jia; Florian Busch; David Flores-Solis; Matthew J Bick; Peilong Lu; Zachary L VanAernum; Aniruddha Sahasrabuddhe; Robert A Langan; Sherry Bermeo; T J Brunette; Vikram Khipple Mulligan; Lauren P Carter; Frank DiMaio; Nikolaos G Sgourakis; Vicki H Wysocki; David Baker
Journal:  Nature       Date:  2018-12-19       Impact factor: 49.962

5.  Skip residues modulate the structural properties of the myosin rod and guide thick filament assembly.

Authors:  Keenan C Taylor; Massimo Buvoli; Elif Nihal Korkmaz; Ada Buvoli; Yuqing Zheng; Nathan T Heinze; Qiang Cui; Leslie A Leinwand; Ivan Rayment
Journal:  Proc Natl Acad Sci U S A       Date:  2015-07-06       Impact factor: 11.205

6.  Rapid search for tertiary fragments reveals protein sequence-structure relationships.

Authors:  Jianfu Zhou; Gevorg Grigoryan
Journal:  Protein Sci       Date:  2014-12-31       Impact factor: 6.725

7.  A Hendecad Motif Is Preferred for Heterochiral Coiled-Coil Formation.

Authors:  Dale F Kreitler; Zhihui Yao; Jay D Steinkruger; David E Mortenson; Lijun Huang; Ritesh Mittal; Benjamin R Travis; Katrina T Forest; Samuel H Gellman
Journal:  J Am Chem Soc       Date:  2019-01-15       Impact factor: 15.419

8.  Mining tertiary structural motifs for assessment of designability.

Authors:  Jian Zhang; Gevorg Grigoryan
Journal:  Methods Enzymol       Date:  2013       Impact factor: 1.600

9.  Structural Stability and Binding Strength of a Designed Peptide-Carbon Nanotube Hybrid.

Authors:  Daniel Roxbury; Shao-Qing Zhang; Jeetain Mittal; William F Degrado; Anand Jagota
Journal:  J Phys Chem C Nanomater Interfaces       Date:  2013-12-12       Impact factor: 4.126

10.  A composite approach towards a complete model of the myosin rod.

Authors:  E Nihal Korkmaz; Keenan C Taylor; Michael P Andreas; Guatam Ajay; Nathan T Heinze; Qiang Cui; Ivan Rayment
Journal:  Proteins       Date:  2015-12-09
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.