Lewinska Marzena, Seitz Christian, Skerra Arne, Schmidtchen Franz P
Institut für Organische Chemie und Biochemie, Technische Universität München, 85747 Garching, Germany.
Bioconjug Chem. 2004 Mar-Apr;15(2):231-4. doi: 10.1021/bc034085f.
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.
蛋白质结构明确的生物共轭物的形成取决于其区域选择性修饰。为实现这一目标,本文描述了一种新方法,即使用商业IgA蛋白酶,通过在水中进行动力学控制的反向蛋白水解,将非天然肽部分连接到预先处理的蛋白质的N端。该过程需要一个H-Ala-Pro N端序列,然后在非变性和非破坏性条件下以可接受的产率提供选择性修饰的共轭物。该方法适用于可进一步修饰的正交部分的N端引入。