ALGORITHMS FOR SELECTING BREAKPOINT LOCATIONS TO OPTIMIZE DIVERSITY IN PROTEIN ENGINEERING BY SITE-DIRECTED PROTEIN RECOMBINATION

Protein engineering by site-directed recombination seeks to develop proteins with new or improved function, by accumulating multiple mutations from a set of homologous parent proteins. A library of hybrid proteins is created by recombining the parent proteins at specified breakpoint locations; subse...

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Vydáno v:Computational Systems Bioinformatics Ročník 6; s. 31 - 40
Hlavní autoři: Zheng, Wei, Ye, Xiaoduan, Friedman, Alan M., Bailey-Kellogg, Chris
Médium: Kapitola Journal Article
Jazyk:angličtina
Vydáno: United States PUBLISHED BY IMPERIAL COLLEGE PRESS AND DISTRIBUTED BY WORLD SCIENTIFIC PUBLISHING CO 2007
Témata:
Algorithms
Base Sequence
Genetic Enhancement - methods
Genetic Variation - genetics
Molecular Sequence Data
Mutagenesis, Site-Directed - methods
Protein Engineering - methods
Proteins - genetics
Proteomics
Recombinant Proteins - genetics
Recombination, Genetic - genetics
Sequence Analysis, DNA - methods
ISBN:1860948723, 9781860948725, 1860948731, 1908979097, 9781860948732, 9781908979094
ISSN:1752-7791
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Shrnutí:Protein engineering by site-directed recombination seeks to develop proteins with new or improved function, by accumulating multiple mutations from a set of homologous parent proteins. A library of hybrid proteins is created by recombining the parent proteins at specified breakpoint locations; subsequent screening/selection identifies hybrids with desirable functional characteristics. In order to improve the frequency of generating novel hybrids, this paper develops the first approach to explicitly plan for diversity in site-directed recombination, including metrics for characterizing the diversity of a planned hybrid library and efficient algorithms for optimizing experiments accordingly. The goal is to choose breakpoint locations to sample sequence space as uniformly as possible (which we argue maximizes diversity), under the constraints imposed by the recombination process and the given set of parents. A dynamic programming approach selects optimal breakpoint locations in polynomial time. Application of our method to optimizing breakpoints for an example biosynthetic enzyme, purE, demonstrates the significance of diversity optimization and the effectiveness of our algorithms.
Bibliografie:ObjectType-Article-1
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content type line 23
ISBN:1860948723
9781860948725
1860948731
1908979097
9781860948732
9781908979094
ISSN:1752-7791
DOI:10.1142/9781860948732_0008