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 language | English |
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| Pages (from-to) | 231-234 |
| Number of pages | 4 |
| Journal | Bioconjugate Chemistry |
| Volume | 15 |
| Issue number | 2 |
| DOIs | |
| State | Published - 2004 |