Literature DB >> 25451785

The CamSol method of rational design of protein mutants with enhanced solubility.

Pietro Sormanni1, Francesco A Aprile1, Michele Vendruscolo2.   

Abstract

Protein solubility is often an essential requirement in biotechnological and biomedical applications. Great advances in understanding the principles that determine this specific property of proteins have been made during the past decade, in particular concerning the physicochemical characteristics of their constituent amino acids. By exploiting these advances, we present the CamSol method for the rational design of protein variants with enhanced solubility. The method works by performing a rapid computational screening of tens of thousand of mutations to identify those with the greatest impact on the solubility of the target protein while maintaining its native state and biological activity. The application to a single-domain antibody that targets the Alzheimer's Aβ peptide demonstrates that the method predicts with great accuracy solubility changes upon mutation, thus offering a cost-effective strategy to help the production of soluble proteins for academic and industrial purposes.
Copyright © 2014. Published by Elsevier Ltd.

Entities:  

Keywords:  protein aggregation; protein solubility

Mesh:

Substances:

Year:  2014        PMID: 25451785     DOI: 10.1016/j.jmb.2014.09.026

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


  108 in total

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