Establishment and evaluation of targeted molecular screening model for the ryanodine receptor or sarco/endoplasmic reticulum calcium ATPase

被引:2
|
作者
Lu, Xiaopeng [1 ]
Jiang, Linlin [1 ]
Chen, Li [1 ]
Ding, Wenwei [1 ]
Wu, Hua [1 ]
Ma, Zhiqing [1 ]
机构
[1] Northwest A&F Univ, Coll Plant Protect, Key Lab Plant Protect Resources & Pest Management, Minist Educ, Yangling 712100, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Mythimna separate; ryanodine receptor; Sarco/endoplasmic reticulum calcium ATPase; Diamide insecticides; Dantrolene; Cyclopiazonic acid; INSECTICIDE CHLORANTRANILIPROLE; CA2+ RELEASE; SERCA; THAPSIGARGIN; ACTIVATOR;
D O I
10.1002/ps.8040
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
BACKGROUD: Endoplasmic reticulum/sarcoplasmic reticulum (ER/SR) is crucial for maintaining intracellular calcium homeostasis due to the calcium-signaling-related proteins on its membrane. While ryanodine receptors (RyR) on insect ER/SR membranes are well-known as targets for diamide insecticides, little is known about other calcium channels. Given the resistance of diamide insecticides, the establishment of molecular screening models targeting RyR or sarco/endoplasmic reticulum calcium ATPase (SERCA) is conducive to the discovery of new insecticidal molecules. RESULTS: The morphological features of Mythimna separata SR have closed vesicles with integrity and high density. The 282 proteins in the SR component contained RyR and SERCA. A measurement model for the release and uptake of calcium was successfully established by detecting calcium ions outside the SR membrane using a fluorescence spectrophotometer. In vitro testing systems using SR vesicles found that diamide insecticides could activate dose-dependently RyR, with EC50 values of 0.14 mu M (Chlorantraniliprole), 0.21 mu M (Flubendiamide), and 0.57 mu M (Cyantraniliprole), respectively. However, dantrolene inhibited RyR-mediated calcium release with an IC50 value of 353.9 mu M, suggesting that dantrolene can weakly antagonize RyR. Moreover, cyclopiazonic acid significantly reduced the enzyme activity and calcium uptake capacity of SERCA. On the contrary, CDN1163 markedly activated the enzyme activity and improved the calcium transport capacity of SERCA. CONCLUSIONS: SR vesicles can be used to study the function of unknown proteins on the SR membranes, as well as for high-throughput screening of highly active compounds targeting RyR or SERCA. (c) 2024 Society of Chemical Industry.
引用
收藏
页码:3369 / 3378
页数:10
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