The Mass Spectrometry society of Japan - The 68th Annual Conference on Mass Spectrometry, Japan

Abstract

Poster Presentations

Day 3, June 24(Fri.)  Room P (501, 502 and 503)

Study of Evaluation Method for Inhibitors of Enzyme Activity Using Substrate Specificity of Aldo-keto Reductase by LC-MS

(1Mukogawa Women's Univ., 2Mukogawa Women's Univ., 3Nara Women's Univ.)
oShihoko Sano1, Shizuyo Horiyama1, Maria Hayashi1, Fumiko Hara1, Chie Honda2, Masayori Hagimori1, Kazuto Nosaka1, Takae Takeuchi3

A member of the human aldo-keto reductase (AKR) superfamily has various biological function and plays an important role, but these enzymes also involved in diseases such as diabetic complications and carcinogenesis. A lot of AKR inhibitors has been developed for the treatment of diseases and novel anticancer drugs, but it is difficult to obtain pharmaceutical approval because high similarities in their amino acid sequences cause side effects due to low specificity. We focused on AKR1B1 and AKR1B10, which is known to be involved in carcinogenesis, and comparative study on enzyme activity and inhibitory effect using synthesized glutathione-conjugated electrophilic carbonyl compound (GSH-CA) which has substrate specificity for these enzymes. In this study, we comfier that HCCFA, selective inhibitor of AKR1B10 inhibits AKR1B10 activity by quantitative analysing reduced products using LC-MS. These results suggest that this new method using GSH-CA and LC-MS can be applied to the evaluation of inhibitors targeting AKR