Reversible modification of DNA by methyltransferase-catalyzed transfer and light-triggered removal of photo-caging groups

Anhäuser L., Muttach F., Rentmeister A.

Research article (journal) | Peer reviewed

Abstract

Methyltransferases are powerful tools for site-specific transfer of non-natural functional groups from synthetic analogs of their cosubstrate S-adenosyl-l-methionine (AdoMet). We present a new class of AdoMet analogs containing photo-caging (PC) groups in their side chain, enzymatic transfer of PC groups by a promiscuous DNA MTase as well as light-triggered removal from the target DNA. This strategy provides a new avenue to reversibly modulate the functionality of DNA at MTase target sites.

Details about the publication

JournalChemical communications (Chem. Commun.)
Volume54
Issue5
Page range449-451
StatusPublished
Release year2017
Language in which the publication is writtenEnglish
DOI10.1039/c7cc08300a
Link to the full texthttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85040542226&origin=inward

Authors from the University of Münster

Anhäuser, Lea
Professorship for Biomolecular Label Chemistry (Prof. Rentmeister)
Muttach, Fabian
Professorship for Biomolecular Label Chemistry (Prof. Rentmeister)
Rentmeister, Andrea
Professorship for Biomolecular Label Chemistry (Prof. Rentmeister)