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2017 Fiscal Year Final Research Report

Elucidation of the molecular determinants of neonicotinoid toxicity

Research Project

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Project/Area Number 16K21507
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Bioorganic chemistry
Biomolecular chemistry
Research InstitutionKindai University

Principal Investigator

IHARA Makoto  近畿大学, 農学部, 准教授 (30466031)

Research Collaborator HIKIDA Mai  
YUKUTA Yoshie  
Project Period (FY) 2016-04-01 – 2018-03-31
Keywordsネオニコチノイド / 殺虫剤 / ニコチン性アセチルコリン受容体 / アセチルコリン結合タンパク質 / イミダクロプリド / チアクロプリド / nAChR
Outline of Final Research Achievements

Neonicotinoids are widely used for crop protection and veterinary use worldwilde. Recently the adverse effects of neonicotinoids have been focused, and some of them were banned from EU. In order to elucidate the molecular mechanism of such adverse effects of neonicotinoids, X-ray crystallography of acetylcholine binding protein, a surrogate protein of ligand binding domain of nicotinic acetylcholine receptors, has been employed and the X-ray crystal structures of AChBP-neonicotinoids complexes were solved. Using those structures, homology models were built and evaluated their interactions. These results suggested that LOOPs D, E and G cooperatively form neonicotinoid-fovored environment in insect nAChRs. Physiological evaluation confirmed that even single mutation at the Loop D, E and G strikingly weakened the neonicotinoid actions on insect nAChRs. These results suggest the adverse effects of neonicotinoids might be controlled through structure guided approaches.

Free Research Field

農薬科学

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Published: 2019-03-29  

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