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Protein Eng Des Sel ; 25(10): 625-30, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22767886

ABSTRACT

Many biotechnology applications require the evolution of enhanced protein stability. Using polymerase chain reaction-based recovery of engineered clones during the screen enrichment phase, we describe a yeast display method capable of yielding engineered proteins having thermal stability that substantially exceeds the viability threshold of the yeast host. To this end, yeast-enhanced green fluorescent protein destabilized by dual-loop insertion was engineered to possess a substantially enhanced resistance to thermal denaturation at 70°C. Stabilized proteins were secreted, purified and found to have three- to six-fold increased resistance to thermal denaturation. The validated method enables yeast display-based screens in previously inaccessible regions of the fitness landscape.


Subject(s)
Green Fluorescent Proteins/chemistry , Green Fluorescent Proteins/genetics , Protein Engineering/methods , Saccharomyces cerevisiae/genetics , Amino Acid Sequence , Models, Molecular , Molecular Sequence Data , Mutagenesis, Insertional , Protein Denaturation , Protein Stability , Temperature
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