A novel method for the N-terminal modification of native proteins

被引:9
|
作者
Lewinska, M
Seitz, C
Skerra, A
Schmidtchen, FP [1 ]
机构
[1] Tech Univ Munich, Inst Organ Chem & Biochem, D-85747 Garching, Germany
[2] Munich Inst Technol, Ctr Life Sci Weihenstephan, D-85350 Freising Weihenstephan, Germany
关键词
D O I
10.1021/bc034085f
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The formation of structurally defined bioconjugates of proteins hinges on their regioselective modification. Toward this goal a novel method is described here using the commercial IgA protease to attach a nonnatural peptidic moiety to the N-terminus of predisposed proteins by means of a kinetically controlled reverse proteolysis in water. The process requires an H-Ala-Pro N-terminal sequence and then furnishes a selectively modified conjugate under nondenaturing and nondestructive conditions in acceptable yield. The method lends itself to the N-terminal introduction of orthogonal moieties that may be elaborated further.
引用
收藏
页码:231 / 234
页数:4
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