Anhäuser L., Muttach F., Rentmeister A.
Research article (journal) | Peer reviewedMethyltransferases 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.
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) |