Literature DB >> 15025517

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

Marzena Lewinska1, Christian Seitz, Arne Skerra, Franz P Schmidtchen.   

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.

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Year:  2004        PMID: 15025517     DOI: 10.1021/bc034085f

Source DB:  PubMed          Journal:  Bioconjug Chem        ISSN: 1043-1802            Impact factor:   4.774


  2 in total

1.  Bioconjugation of green fluorescent protein via an unexpectedly stable cyclic sulfonium intermediate.

Authors:  Ramiz Nathani; Paul Moody; Mark E B Smith; Richard J Fitzmaurice; Stephen Caddick
Journal:  Chembiochem       Date:  2012-05-25       Impact factor: 3.164

2.  A two-trick pony: lysosomal protease cathepsin B possesses surprising ligase activity.

Authors:  Tyler R Lambeth; Zhefu Dai; Yong Zhang; Ryan R Julian
Journal:  RSC Chem Biol       Date:  2021-02-17
  2 in total

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