Engineered SAM Synthetases for Enzymatic Generation of AdoMet Analogs with Photocaging Groups and Reversible DNA Modification in Cascade Reactions. Issue 1 (13th November 2020)

• Record Type: Journal Article
• Authors: Michailidou, Freideriki; Klöcker, Nils; Cornelissen, Nicolas V.; Singh, Rohit K.; Peters, Aileen; Ovcharenko, Anna; Kümmel, Daniel; Rentmeister, Andrea
• Is Part Of: Angewandte Chemie international edition. Volume 60:Issue 1(2021)
• Page Start: 480
• Page End: 485
• Publication Date: 2020-11-13
• Subjects: bioorthogonal -- MAT -- photocaging -- protein engineering -- SAM; Chemistry -- Periodicals; 540
• DOI: 10.1002/anie.202012623
• Languages: English
• ISSNs: 1433-7851

Abstract

Abstract: Methylation and demethylation of DNA, RNA and proteins has emerged as a major regulatory mechanism. Studying the function of these modifications would benefit from tools for their site‐specific inhibition and timed removal. S ‐Adenosyl‐L‐methionine (AdoMet) analogs in combination with methyltransferases (MTases) have proven useful to map or block and release MTase target sites, however their enzymatic generation has been limited to aliphatic groups at the sulfur atom. We engineered a SAM synthetase from Cryptosporidium hominis (PC‐ChMAT) for efficient generation of AdoMet analogs with photocaging groups that are not accepted by any WT MAT reported to date. The crystal structure of PC‐ChMAT at 1.87 Å revealed how the photocaged AdoMet analog is accommodated and guided engineering of a thermostable MAT from Methanocaldococcus jannaschii . PC‐MATs were compatible with DNA‐ and RNA‐MTases, enabling sequence‐specific modification ("writing") of plasmid DNA and light‐triggered removal ("erasing"). Abstract : S ‐Adenosyl‐L‐methionine (AdoMet) analogs provide a way to study and control methyltransferase target sites. Their enzymatic generation has been limited to aliphatic groups at the sulfur atom. We engineered and crystallized the first SAM synthetases (PC‐MATs) able to generate AdoMet analogs with photocaging groups. In combination with DNA‐MTases, sequence‐specific modification ("writing") of plasmid DNA and light‐triggered removal ("erasing") is demonstrated.