Literature DB >> 19569186

Alpha helical crossovers favor right-handed supersecondary structures by kinetic trapping: the phone cord effect in protein folding.

Benjamin J Cole1, Christopher Bystroff.   

Abstract

The remarkable predominance of right-handedness in beta-alpha-beta helical crossovers has been previously explained in terms of thermodynamic stability and kinetic accessibility, but a different kinetic trapping mechanism may also play a role. If the beta-sheet contacts are made before the crossover helix is fully formed, and if the backbone angles of the folding helix follows the energetic pathway of least resistance, then the helix would impart a torque on the ends of the two strands. Such a torque would tear apart a left-handed conformation but hold together a right-handed one. Right-handed helical crossovers predominate even in all-alpha proteins, where previous explanations based on the preferred twist of the beta sheet do not apply. Using simple molecular simulations, we can reproduce the right-handed preference in beta-alpha-beta units, without imposing specific beta-strand geometry. The new kinetic trapping mechanism is dubbed the "phone cord effect" because it is reminiscent of the way a helical phone cord forms superhelices to relieve torsional stress. Kinetic trapping explains the presence of a right-handed superhelical preference in alpha helical crossovers and provides a possible folding mechanism for knotted proteins.

Mesh:

Year:  2009        PMID: 19569186      PMCID: PMC2776948          DOI: 10.1002/pro.182

Source DB:  PubMed          Journal:  Protein Sci        ISSN: 0961-8368            Impact factor:   6.725


  22 in total

1.  A deeply knotted protein structure and how it might fold.

Authors:  W R Taylor
Journal:  Nature       Date:  2000-08-24       Impact factor: 49.962

2.  Revisiting the Ramachandran plot: hard-sphere repulsion, electrostatics, and H-bonding in the alpha-helix.

Authors:  Bosco K Ho; Annick Thomas; Robert Brasseur
Journal:  Protein Sci       Date:  2003-11       Impact factor: 6.725

3.  Helix propensities of short peptides: molecular dynamics versus bioinformatics.

Authors:  Christopher Bystroff; Shekhar Garde
Journal:  Proteins       Date:  2003-03-01

4.  Investigations into sequence and conformational dependence of backbone entropy, inter-basin dynamics and the Flory isolated-pair hypothesis for peptides.

Authors:  Muhammad H Zaman; Min-Yi Shen; R Stephen Berry; Karl F Freed; Tobin R Sosnick
Journal:  J Mol Biol       Date:  2003-08-15       Impact factor: 5.469

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Authors:  J S Richardson
Journal:  Proc Natl Acad Sci U S A       Date:  1976-08       Impact factor: 11.205

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Authors:  M J Sternberg; J M Thornton
Journal:  J Mol Biol       Date:  1976-08-15       Impact factor: 5.469

7.  Energy of stabilization of the right-handed beta alpha beta crossover in proteins.

Authors:  K C Chou; G Némethy; M Pottle; H A Scheraga
Journal:  J Mol Biol       Date:  1989-01-05       Impact factor: 5.469

Review 8.  Boltzmann's principle, knowledge-based mean fields and protein folding. An approach to the computational determination of protein structures.

Authors:  M J Sippl
Journal:  J Comput Aided Mol Des       Date:  1993-08       Impact factor: 3.686

9.  Stereochemical criteria for polypeptide and protein chain conformations. II. Allowed conformations for a pair of peptide units.

Authors:  C Ramakrishnan; G N Ramachandran
Journal:  Biophys J       Date:  1965-11       Impact factor: 4.033

10.  Simulating protein folding initiation sites using an alpha-carbon-only knowledge-based force field.

Authors:  Patrick M Buck; Christopher Bystroff
Journal:  Proteins       Date:  2009-08-01
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  6 in total

1.  The Structural Rule Distinguishing a Superfold: A Case Study of Ferredoxin Fold and the Reverse Ferredoxin Fold.

Authors:  Takumi Nishina; Megumi Nakajima; Masaki Sasai; George Chikenji
Journal:  Molecules       Date:  2022-05-31       Impact factor: 4.927

2.  Mapping the Geometric Evolution of Protein Folding Motor.

Authors:  Gaurav Jerath; Prakash Kishore Hazam; Shashi Shekhar; Vibin Ramakrishnan
Journal:  PLoS One       Date:  2016-10-07       Impact factor: 3.240

3.  Modeling protein folding in vivo.

Authors:  Irina Sorokina; Arcady Mushegian
Journal:  Biol Direct       Date:  2018-07-06       Impact factor: 4.540

4.  Integron gene cassettes: a repository of novel protein folds with distinct interaction sites.

Authors:  Visaahini Sureshan; Chandrika N Deshpande; Yan Boucher; Jeremy E Koenig; H W Stokes; Stephen J Harrop; Paul M G Curmi; Bridget C Mabbutt
Journal:  PLoS One       Date:  2013-01-18       Impact factor: 3.240

5.  Structure of the human MLH1 N-terminus: implications for predisposition to Lynch syndrome.

Authors:  Hong Wu; Hong Zeng; Robert Lam; Wolfram Tempel; Iain D Kerr; Jinrong Min
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2015-07-28       Impact factor: 1.056

6.  Role of Backbone Dipole Interactions in the Formation of Secondary and Supersecondary Structures of Proteins.

Authors:  Sai J Ganesan; S Matysiak
Journal:  J Chem Theory Comput       Date:  2014-05-09       Impact factor: 6.006

  6 in total

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