Rempel Brian P, Price Eric W, Phenix Christopher P
1 Department of Science, Augustana Faculty, University of Alberta, Edmonton, Alberta, Canada.
2 Department of Chemistry, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Mol Imaging. 2017 Jan-Dec;16:1536012117717852. doi: 10.1177/1536012117717852.
Hydrolytic enzymes are a large class of biological catalysts that play a vital role in a plethora of critical biochemical processes required to maintain human health. However, the expression and/or activity of these important enzymes can change in many different diseases and therefore represent exciting targets for the development of positron emission tomography (PET) and single-photon emission computed tomography (SPECT) radiotracers. This review focuses on recently reported radiolabeled substrates, reversible inhibitors, and irreversible inhibitors investigated as PET and SPECT tracers for imaging hydrolytic enzymes. By learning from the most successful examples of tracer development for hydrolytic enzymes, it appears that an early focus on careful enzyme kinetics and cell-based studies are key factors for identifying potentially useful new molecular imaging agents.
水解酶是一大类生物催化剂,在维持人体健康所需的众多关键生化过程中发挥着至关重要的作用。然而,这些重要酶的表达和/或活性在许多不同疾病中会发生变化,因此成为正电子发射断层扫描(PET)和单光子发射计算机断层扫描(SPECT)放射性示踪剂开发的热门靶点。本综述重点关注最近报道的作为PET和SPECT示踪剂用于成像水解酶的放射性标记底物、可逆抑制剂和不可逆抑制剂。通过借鉴水解酶示踪剂开发最成功的例子,早期专注于仔细的酶动力学和基于细胞的研究似乎是识别潜在有用的新型分子成像剂的关键因素。