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Engineering of protease variants exhibiting altered substrate specificity

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Abstract
By using an improved genetic screening system, variants of the HAV 3CP protease which exhibit altered P2 specificity were obtained. We randomly mutated the His145, Lys146, Lys147, and Leu155 residues that constitute the S2 pocket of 3CP and then isolated variants that preferred substrates with Gln over the original Thr at the P2 position using a yeast-based screening method. One of the isolated variants cleaved the Gln-containing peptide substrate more efficiently in vitro, proving the efficiency of our method in isolating engineered proteases with desired substrate selectivity. (c) 2008 Elsevier Inc. All rights reserved.
Author(s)
Sellamuthu, SaravananShin, Bae HyunLee, Eui SeungRho, Seong-HwanHwang, WangtaekLee, Yong JaeHan, Hye-EunKim, Jae IlPark, Woo Jin
Issued Date
2008-06
Type
Article
DOI
10.1016/j.bbrc.2008.04.026
URI
https://scholar.gist.ac.kr/handle/local/17371
Publisher
Academic Press
Citation
Biochemical and Biophysical Research Communications, v.371, no.1, pp.122 - 126
ISSN
0006-291X
Appears in Collections:
Department of Life Sciences > 1. Journal Articles
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