Bandarian Vahe
Department of Chemistry, University of Utah, 315 S 1400 E, Salt Lake City, Utah 84112, United States.
ACS Bio Med Chem Au. 2022 Jun 15;2(3):187-195. doi: 10.1021/acsbiomedchemau.1c00059. Epub 2022 Feb 28.
Radical -adenosyl-l-methionine (SAM) enzymes catalyze a diverse group of complex transformations in all aspects of cellular physiology. These metalloenzymes bind SAM to a 4Fe-4S cluster and reductively cleave SAM to generate a 5'-deoxyadenosyl radical, which generally initiates the catalytic cycle by catalyzing a H atom to activate the substrate for subsequent chemistry. This perspective will focus on our discovery of several members of this superfamily of enzymes, with a particular emphasis on the current state of the field, challenges, and outlook.
自由基 - 腺苷甲硫氨酸(SAM)酶在细胞生理学的各个方面催化各种各样的复杂转化反应。这些金属酶将SAM与一个4Fe-4S簇结合,并还原裂解SAM以生成一个5'-脱氧腺苷自由基,该自由基通常通过催化一个氢原子来激活底物以启动后续化学反应,从而开启催化循环。本文将重点介绍我们对该酶超家族中几个成员的发现,特别强调该领域的现状、挑战和前景。