A nonpeptidal peptidomimetic agonist of the insect FLRFamide myosuppressin family

被引:24
作者
Nachman, RJ
Olender, EH
Roberts, VA
Holman, GM
Yamamoto, D
机构
[1] SCRIPPS RES INST, DEPT MOLEC BIOL, LA JOLLA, CA 92037 USA
[2] MITSUBISHI KASEI INST LIFE SCI, NEUROPHYSIOL LAB, TOKYO 11, JAPAN
关键词
peptidomimetic; FMRFamide; cockroach; locust; myoinhibition; molecular dynamics; neuromuscular junction; ligand; binding; NDGA; arachidonic acid; lipoxygenase;
D O I
10.1016/0196-9781(95)02097-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Benzethonium chloride (Bztc) is the first totally nonpeptide ligand for an insect, indeed an invertebrate, peptide receptor. Bztc mimics the inhibitory physiological activity of the myosuppressins, a subfamily of the FLRFamides, in three different insect bioassay systems. The inhibitory action of leucomyosuppressin and the nonpeptide Bztc in both the cockroach hindgut and the mealworm neuromuscular junction can be blocked by the lipoxygenase inhibitor, nordihydroguaiaretic acid, providing evidence for similar modes of action. Lipoxygenase metabolites of arachidonic acid may mediate inhibition of neuromuscular transmission by these two factors. In addition, Bztc competitively displaces a radiolabeled myosuppressin analogue from high- and low-affinity receptors of the locust oviduct. Thus, the nonpeptide interacts with both binding and activating regions of myosuppressin receptors. Molecular dynamics experiments in which selected functional groups of Bztc were fit onto corresponding functional groups of low-energy myosuppressin pentapeptide structures indicate how Bztc may mimic the myosuppressins at a molecular level. The discovery of Bztc as a nonpeptidal peptidomimetic analogue provides an opportunity to develop new pest management strategies by targeting an insect's own peptide receptor.
引用
收藏
页码:313 / 320
页数:8
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