dc.creatorRULLER, Roberto
dc.creatorSILVA-ROCHA, Rafael
dc.creatorSILVA, Artur
dc.creatorSCHNEIDER, Maria Paula Cruz
dc.creatorWARD, Richard John
dc.date.accessioned2012-10-19T14:14:45Z
dc.date.accessioned2018-07-04T15:01:39Z
dc.date.available2012-10-19T14:14:45Z
dc.date.available2018-07-04T15:01:39Z
dc.date.created2012-10-19T14:14:45Z
dc.date.issued2011
dc.identifierBIOCHEMISTRY AND MOLECULAR BIOLOGY EDUCATION, v.39, n.1, p.21-27, 2011
dc.identifier1470-8175
dc.identifierhttp://producao.usp.br/handle/BDPI/20801
dc.identifier10.1002/bmb.20430
dc.identifierhttp://dx.doi.org/10.1002/bmb.20430
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1617580
dc.description.abstractProtein engineering is a powerful tool, which correlates protein structure with specific functions, both in applied biotechnology and in basic research. Here, we present a practical teaching course for engineering the green fluorescent protein (GFP) from Aequorea victoria by a random mutagenesis strategy using error-prone polymerase chain reaction. Screening of bacterial colonies transformed with random mutant libraries identified GFP variants with increased fluorescence yields. Mapping the three-dimensional structure of these mutants demonstrated how alterations in structural features such as the environment around the fluorophore and properties of the protein surface can influence functional properties such as the intensity of fluorescence and protein solubility.
dc.languageeng
dc.publisherWILEY-BLACKWELL
dc.relationBiochemistry and Molecular Biology Education
dc.rightsCopyright WILEY-BLACKWELL
dc.rightsrestrictedAccess
dc.subjectDirected evolution
dc.subjecterror-prone PCR
dc.subjectgreen fluorescent protein
dc.subjectrandom mutagenesis
dc.subjectrecombinant protein expression
dc.titleA Practical Teaching Course in Directed Protein Evolution Using the Green Fluorescent Protein as a Model
dc.typeArtículos de revistas


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