OAK

Engineering of protease variants exhibiting altered substrate specificity

Metadata Downloads
Author(s)
Sellamuthu, SaravananShin, Bae HyunLee, Eui SeungRho, Seong-HwanHwang, WangtaekLee, Yong JaeHan, Hye-EunKim, Jae IlPark, Woo Jin
Type
Article
Citation
Biochemical and Biophysical Research Communications, v.371, no.1, pp.122 - 126
Issued Date
2008-06
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.
Publisher
Academic Press
ISSN
0006-291X
DOI
10.1016/j.bbrc.2008.04.026
URI
https://scholar.gist.ac.kr/handle/local/17371
Authorize & License
  • Authorize공개
Files in This Item:
  • There are no files associated with this item.

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.