Literature DB >> 16544054

Genetic algorithms as a tool for helix design--computational and experimental studies on prion protein helix 1.

Jan Ziegler1, Stephan Schwarzinger.   

Abstract

Evolutionary computing is a general optimization mechanism successfully implemented for a variety of numeric problems in a variety of fields, including structural biology. We here present an evolutionary approach to optimize helix stability in peptides and proteins employing the AGADIR energy function for helix stability as scoring function. With the ability to apply masks determining positions, which are to remain constant or fixed to a certain class of amino acids, our algorithm is capable of developing stable helical scaffolds containing a wide variety of structural and functional amino acid patterns. The algorithm showed good convergence behaviour in all tested cases and can be parameterized in a wide variety of ways. We have applied our algorithm for the optimization of the stability of prion protein helix 1, a structural element of the prion protein which is thought to play a crucial role in the conformational transition from the cellular to the pathogenic form of the prion protein, and which therefore poses an interesting target for pharmacological as well as genetic engineering approaches to counter the as of yet uncurable prion diseases. NMR spectroscopic investigations of selected stabilizing and destabilizing mutations found by our algorithm could demonstrate its ability to create stabilized variants of secondary structure elements.

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Year:  2006        PMID: 16544054     DOI: 10.1007/s10822-006-9035-5

Source DB:  PubMed          Journal:  J Comput Aided Mol Des        ISSN: 0920-654X            Impact factor:   3.686


  51 in total

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Journal:  Curr Opin Chem Biol       Date:  2001-12       Impact factor: 8.822

2.  Protein design is NP-hard.

Authors:  Niles A Pierce; Erik Winfree
Journal:  Protein Eng       Date:  2002-10

3.  Display of active subtilisin 309 on phage: analysis of parameters influencing the selection of subtilisin variants with changed substrate specificity from libraries using phosphonylating inhibitors.

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Journal:  J Mol Biol       Date:  2000-02-11       Impact factor: 5.469

4.  The meaning of hydrophobicity.

Authors:  K A Dill
Journal:  Science       Date:  1990-10-12       Impact factor: 47.728

5.  Energy functions for protein design: adjustment with protein-protein complex affinities, models for the unfolded state, and negative design of solubility and specificity.

Authors:  Navin Pokala; Tracy M Handel
Journal:  J Mol Biol       Date:  2005-01-20       Impact factor: 5.469

Review 6.  Helix capping.

Authors:  R Aurora; G D Rose
Journal:  Protein Sci       Date:  1998-01       Impact factor: 6.725

7.  Solubilized, spaced polyalanines: a context-free system for determining amino acid alpha-helix propensities.

Authors:  Justin S Miller; Robert J Kennedy; Daniel S Kemp
Journal:  J Am Chem Soc       Date:  2002-02-13       Impact factor: 15.419

8.  Elucidating the folding problem of helical peptides using empirical parameters. III. Temperature and pH dependence.

Authors:  V Muñoz; L Serrano
Journal:  J Mol Biol       Date:  1995-01-20       Impact factor: 5.469

9.  The (i, i + 4) Phe-His interaction studied in an alanine-based alpha-helix.

Authors:  K M Armstrong; R Fairman; R L Baldwin
Journal:  J Mol Biol       Date:  1993-03-05       Impact factor: 5.469

10.  High-affinity binders selected from designed ankyrin repeat protein libraries.

Authors:  H Kaspar Binz; Patrick Amstutz; Andreas Kohl; Michael T Stumpp; Christophe Briand; Patrik Forrer; Markus G Grütter; Andreas Plückthun
Journal:  Nat Biotechnol       Date:  2004-04-18       Impact factor: 54.908

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