help button home button Biophys. J.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Originally published as Biophys J. BioFAST on March 2, 2006.
doi:10.1529/biophysj.105.079277
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
biophysj.105.079277v1
90/11/4167    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Saraf, M. C.
Right arrow Articles by Maranas, C. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Saraf, M. C.
Right arrow Articles by Maranas, C. D.
Biophysical Journal 90:4167-4180 (2006)
© 2006 The Biophysical Society

IPRO: An Iterative Computational Protein Library Redesign and Optimization Procedure

Manish C. Saraf *, Gregory L. Moore {dagger}, Nina M. Goodey {ddagger}, Vania Y. Cao {ddagger}, Stephen J. Benkovic {ddagger} and Costas D. Maranas *

* Department of Chemical Engineering, The Pennsylvania State University, University Park, Pennsylvania 16802; {dagger} Xencor Inc., Monrovia, California 91016; and {ddagger} Department of Chemistry, The Pennsylvania State University, University Park, Pennsylvania 16802

Correspondence: Address reprint requests to Costas D. Maranas, Tel.: 814-863-9958; Fax: 814-865-7846; E-mail: costas{at}psu.edu.

A number of computational approaches have been developed to reengineer promising chimeric proteins one at a time through targeted point mutations. In this article, we introduce the computational procedure IPRO (iterative protein redesign and optimization procedure) for the redesign of an entire combinatorial protein library in one step using energy-based scoring functions. IPRO relies on identifying mutations in the parental sequences, which when propagated downstream in the combinatorial library, improve the average quality of the library (e.g., stability, binding affinity, specific activity, etc.). Residue and rotamer design choices are driven by a globally convergent mixed-integer linear programming formulation. Unlike many of the available computational approaches, the procedure allows for backbone movement as well as redocking of the associated ligands after a prespecified number of design iterations. IPRO can also be used, as a limiting case, for the redesign of a single or handful of individual sequences. The application of IPRO is highlighted through the redesign of a 16-member library of Escherichia coli/Bacillus subtilis dihydrofolate reductase hybrids, both individually and through upstream parental sequence redesign, for improving the average binding energy. Computational results demonstrate that it is indeed feasible to improve the overall library quality as exemplified by binding energy scores through targeted mutations in the parental sequences.




This article has been cited by other articles:


Home page
Biophys. JHome page
H. Fazelinia, P. C. Cirino, and C. D. Maranas
Extending Iterative Protein Redesign and Optimization (IPRO) in Protein Library Design for Ligand Specificity
Biophys. J., March 15, 2007; 92(6): 2120 - 2130.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2006 by the Biophysical Society.