A Novel Method for the N-Terminal Modification of Native Proteins

Marzena Lewinska, Christian Seitz, Arne Skerra, Franz P. Schmidtchen

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)231-234
Number of pages4
JournalBioconjugate Chemistry
Volume15
Issue number2
DOIs
StatePublished - 2004

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