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2017 Fiscal Year Final Research Report

Analysis of regulatory mechanism of human FoF1-ATP synthase

Research Project

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Project/Area Number 15K07014
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Functional biochemistry
Research InstitutionThe University of Tokyo

Principal Investigator

Suzuki Toshiharu  東京大学, 大学院工学系研究科(工学部), 主幹研究員 (60618809)

Project Period (FY) 2015-04-01 – 2018-03-31
KeywordsFoF1-ATP synthase / F1-ATPase / ATP
Outline of Final Research Achievements

In this project, I established heterologous expression, microscopic single-molecule analysis and X-ray crystallographic systems for bovine F1-ATPase which has high structural similarity to human F1. By using the systems, effects of resveratrol, which has been suggested to have positive effects of extending lifetime and curing adult diseases of eukaryotes, have been analyzed as a model inhibitor for mammalian F1. As a result, resveratrol was suggested to inhibit the ATP-synthesis turnover by preventing the elementary step of product phosphate-binding by binding to the cleft formed between the rotor and stator subunits of bovine F1. This finding would become a theoretical basis to artificially control the energy system of mammalian species in future.

Free Research Field

構造生物学

URL: 

Published: 2019-03-29  

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