Department of Biochemistry, Case Western Reserve University School of Medicine, 10900 Euclid Ave., Cleveland, OH 44106, USA.
Molecules. 2013 Aug 2;18(8):9278-92. doi: 10.3390/molecules18089278.
Kinetic isotope effects (KIEs) are a very powerful tool for investigating enzyme mechanisms. Precision of measurement is the most important factor for KIE determinations, especially for small heavy atom KIEs. Internal competition is commonly used to measure small KIEs on V/K. Several methods, including such as liquid scintillation counting, mass spectrometry, nuclear magnetic resonance spectroscopy and polarimetry have been used to determine KIEs. In this paper, which does not aspire to be an exhaustive review, we briefly review different experimental approaches for the measurement of KIEs on enzymatic reaction with an emphasis on newer techniques employing mass spectrometry and nuclear magnetic resonance spectrometry as well as some corresponding examples.
动力学同位素效应(KIEs)是研究酶机制的非常有力的工具。测量的精度是 KIE 测定的最重要因素,特别是对于小重原子 KIEs。内部竞争通常用于测量 V/K 上的小 KIE。已经使用了几种方法,包括液体闪烁计数、质谱、核磁共振波谱和偏振测量来确定 KIE。本文无意进行详尽的综述,我们简要回顾了测量酶反应中 KIE 的不同实验方法,重点介绍了使用质谱和核磁共振波谱的新技术以及一些相应的例子。