Ryanodine Receptor as Insecticide Target

被引:17
作者
Samurkas, Arthur [1 ,2 ]
Yao, Li [1 ]
Hadiatullah, Hadiatullah [1 ]
Ma, Ruifang [1 ]
Xie, Yunxuan [3 ]
Sundarraj, Rajamanikandan [1 ]
Zuilhof, Han [1 ,2 ,4 ]
Yuchi, Zhiguang [1 ]
机构
[1] Tianjin Univ, Collaborat Innovat Ctr Chem Sci & Engn, Sch Pharmaceut Sci & Technol, Tianjin Key Lab Modern Drug Delivery & High Effic, Tianjin 300072, Peoples R China
[2] Wageningen Univ & Res, Lab Organ Chem, Stippeneng 4,4, NL-6708 WE Wageningen, Netherlands
[3] Tianjin Univ, Sch Environm Sci & Engn, Tianjin 300072, Peoples R China
[4] King Abdulaziz Univ, Fac Engn, Dept Chem & Mat Engn, Jeddah 21629, Saudi Arabia
基金
中国国家自然科学基金;
关键词
Ryanodine receptor; insecticide; resistance; target; diamide; structural biology; XYLOSTELLA LEPIDOPTERA PLUTELLIDAE; CALCIUM-RELEASE CHANNEL; RABBIT SKELETAL-MUSCLE; DIAMIDE INSECTICIDES; ANTHRANILIC DIAMIDE; DIAMONDBACK MOTH; CRYSTAL-STRUCTURE; RESISTANCE; CHLORANTRANILIPROLE; DOMAIN;
D O I
10.2174/1381612827666210902150224
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The ryanodine receptor (RyR) is one of the primary targets of commercial insecticides. The diamide insecticide family, including flubendiamide, chlorantraniliprole, cyantraniliprole, etc., targets insect RyRs and can be used to control a wide range of destructive agricultural pests. The diamide insecticides are highly selective against lepidopteran and coleopteran pests with relatively low toxicity for non-target species, such as mammals, fishes, and beneficial insects. However, recently mutations identified on insect RyRs have emerged and caused resistance in several major agricultural pests throughout different continents. This review paper summarizes the recent findings on the structure and function of insect RyRs as insecticide targets. Specifically, we examine the structures of RyRs from target and non-target species, which reveals the molecular basis for insecticide action and selectivity. We also examine the structural and functional changes of RyR caused by the resistance mutations. Finally, we examine the progress in RyR structure-based insecticide design and discuss how this might help the development of a new generation of green insecticides.
引用
收藏
页码:26 / 35
页数:10
相关论文
共 61 条
[1]   Detection of a ryanodine receptor target-site mutation in diamide insecticide resistant fall armyworm, Spodoptera frugiperda [J].
Boaventura, Debora ;
Bolzan, Anderson ;
Padovez, Fernando E. O. ;
Okuma, Daniela M. ;
Omoto, Celso ;
Nauen, Ralf .
PEST MANAGEMENT SCIENCE, 2020, 76 (01) :47-54
[2]  
Casida JE, 2017, TOXICOL RES-UK, V6, P755, DOI [10.1039/c7tx00198c, 10.1039/C7TX00198C]
[3]   Anthranilic diamides: A new class of insecticides with a novel mode of action, ryanodine receptor activation [J].
Cordova, D ;
Benner, EA ;
Sacher, MD ;
Rauh, JJ ;
Sopa, JS ;
Lahm, GP ;
Selby, TP ;
Stevenson, TM ;
Flexner, L ;
Gutteridge, S ;
Rhoades, DF ;
Wu, L ;
Smith, RM ;
Tao, Y .
PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, 2006, 84 (03) :196-214
[4]  
Cordova D., 2007, Pesticide Chemistry, Crop Protection, Public Health, and Environmental Safety, P121
[5]  
Cordova Daniel, 2007, V948, P223
[6]   Investigation of the contribution of RyR target-site mutations in diamide resistance by CRISPR/Cas9 genome modification in Drosophila [J].
Douris, Vassilis ;
Papapostolou, Kyriaki-Maria ;
Ilias, Aris ;
Roditakis, Emmanuel ;
Kounadi, Styliani ;
Riga, Maria ;
Nauen, Ralf ;
Vontas, John .
INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2017, 87 :127-135
[7]   Ca2+ inactivation sites are located in the COOH-terminal quarter of recombinant rabbit skeletal muscle Ca2+ release channels (ryanodine receptors) [J].
Du, GG ;
MacLennan, DH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (37) :26120-26126
[8]   Phthalic acid diamides activate ryanodine-sensitive Ca2+ release channels in insects [J].
Ebbinghaus-Kintscher, U ;
Luemmen, P ;
Lobitz, N ;
Schulte, T ;
Funke, C ;
Fischer, R ;
Masaki, T ;
Yasokawa, N ;
Tohnishi, M .
CELL CALCIUM, 2006, 39 (01) :21-33
[9]   MOLECULAR-STRUCTURE AND TISSUE DISTRIBUTION OF RYANODINE RECEPTORS CALCIUM CHANNELS [J].
GIANNINI, G ;
SORRENTINO, V .
MEDICINAL RESEARCH REVIEWS, 1995, 15 (04) :313-323
[10]   Novel diamide insecticides: Sulfoximines, sulfonimidamides and other new sulfonimidoyl derivatives [J].
Gnamm, Christian ;
Jeanguenat, Andre ;
Dutton, Ana C. ;
Grimm, Christoph ;
Kloer, Daniel P. ;
Crossthwaite, Andrew J. .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2012, 22 (11) :3800-3806