Abstract
Meta- and para-phenylenediamines have recently been shown to catalyze oxime and hydrazone ligation reactions at rates much faster than aniline, a commonly used catalyst. Here, we demonstrate how these new catalysts can be used in a generally applicable procedure for fluorescent labeling, PEGylation, immobilization, and release of aldehyde- and ketone- functionalized proteins. The chemical orthogonality of phenylenediamine-catalyzed oxime ligation versus copper-catalyzed click reaction has also been harnessed for simultaneous dual labeling of bifunctional proteins containing both aldehyde and alkyne groups in high yield.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 15.4.1-15.4.28 |
| Journal | Current Protocols in Protein Science |
| Volume | 2015 |
| DOIs | |
| State | Published - 2015 |
Bibliographical note
Publisher Copyright:© 2014 by John Wiley & Sons, Inc.
Keywords
- Dual protein labeling
- Hydrazone ligation
- Meta-phenylenediamine
- Oxime ligation
- Para-phenylenediamine
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