Mechanism of protein splicing of the Pyrococcus abyssi lon protease intein

被引:4
|
作者
O'Brien, Kevin M. [1 ]
Schufreider, Ann K. [1 ]
McGill, Melissa A. [1 ]
O'Brien, Kathryn M. [1 ]
Reitter, Julie N. [1 ]
Mills, Kenneth V. [1 ]
机构
[1] Coll Holy Cross, Dept Chem, Worcester, MA 01610 USA
基金
美国国家科学基金会;
关键词
Protein splicing; Intein; Extein; Pyrococcus abyssi; Lon protease; Homing endonuclease; CRYSTAL-STRUCTURE; MINI-INTEIN; CLEAVAGE; ELEMENTS; INTERMEDIATE; PURIFICATION; MODULATION; REVEALS; AMINO;
D O I
10.1016/j.bbrc.2010.11.055
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein splicing is a post-translational process by which an intervening polypeptide, the intein, excises itself from the flanking polypeptides, the exteins, coupled to ligation of the exteins. The Ion protease of Pyrococcus abyssi (Pab) is interrupted by an intein. When over-expressed as a fusion protein in Escherichia colt, the Pab Ion protease intein can promote efficient protein splicing. Mutations that block individual steps of splicing generally do not lead to unproductive side reactions, suggesting that the intein tightly coordinates the splicing process. The intein can splice, although it has Lys in place of the highly conserved penultimate His, and mutants of the intein in the C-terminal region lead to the accumulation of stable branched-ester intermediate. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:457 / 461
页数:5
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