A highly selective and sensitive fluorescence probe for a specific binding site on insect ryanodine receptors. Issue 1 (1st June 2020)

• Record Type: Journal Article
• Authors: Liao, Min; Li, Qibo; Yang, Zhikun; Feng, Tong; Xu, Zhiyuan; Liu, Qing; Liu, Shangzhong
• Is Part Of: Annals of the New York Academy of Sciences. Volume 1475:Issue 1(2020)
• Page Start: 43
• Page End: 51
• Publication Date: 2020-06-01
• Subjects: ryanodine receptors -- fluorescence probe -- insecticide -- phthalic diamide; Medical sciences -- Periodicals; Medicine -- Periodicals; Science -- Periodicals; 610
• DOI: 10.1111/nyas.14362
• Languages: English
• ISSNs: 0077-8923

Abstract

Abstract: There is a significant need to study the binding of active compounds to the specific sites on insect ryanodine receptors (RyRs) that are the targets of two novel classes of diamide insecticides to which insects are becoming increasingly resistant. Here, we describe a rapid assay to study the action of potential compounds on the flubendiamide (Flu) binding site of insect RyRs that uses a fluorescence polarization assay with the fluorescence probe Flu‐R‐L that we synthesized. The IC50 of Flu for inhibiting probe binding on insect RyR was 18.82 ng/mL. The binding of 86 novel phthalic diamide derivatives on insect RyRs was studied using this newly established assay, and the compounds that exhibited high‐affinity binding in the assay also possessed in vivo insecticidal activity against Plutella xylostella . Thus, Flu‐R‐L is a highly selective and sensitive fluorescence probe for studying the binding affinity of novel compounds to the Flu binding site of insect RyRs. The assay based on Flu‐R‐L is a rapid, accurate, and sensitive method for the screening of potentially bioactive molecules that bind specifically to insect RyRs. Abstract : There is a significant need to study the binding of active compounds to the specific sites on insect ryanodine receptors that are the targets of two novel classes of diamide insecticides to which insects are becoming increasingly resistant. Here, we describe a rapid assay to study the action of potential compounds on the flubendiamide binding site of insect RyRs using a fluorescence probe that we synthesized.