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冈比亚按蚊精浆转谷氨酰胺酶AgTG3的二氢异恶唑抑制剂

Dihydroisoxazole inhibitors of Anopheles gambiae seminal transglutaminase AgTG3.

作者信息

Le Binh V, Klöck Cornelius, Schatz Alexandra, Nguyen Jennifer B, Kakani Evdoxia G, Catteruccia Flaminia, Khosla Chaitan, Baxter Richard H G

机构信息

Department of Chemistry, Yale University, P,O, Box 208107, New Haven, CT 06520-8107, USA.

出版信息

Malar J. 2014 Jun 2;13:210. doi: 10.1186/1475-2875-13-210.

Abstract

BACKGROUND

Current vector-based malaria control strategies are threatened by the rise of biochemical and behavioural resistance in mosquitoes. Researching mosquito traits of immunity and fertility is required to find potential targets for new vector control strategies. The seminal transglutaminase AgTG3 coagulates male Anopheles gambiae seminal fluids, forming a 'mating plug' that is required for male reproductive success. Inhibitors of AgTG3 can be useful both as chemical probes of A. gambiae reproductive biology and may further the development of new chemosterilants for mosquito population control.

METHODS

A targeted library of 3-bromo-4,5-dihydroxoisoxazole inhibitors were synthesized and screened for inhibition of AgTG3 in a fluorescent, plate-based assay. Positive hits were tested for in vitro activity using cross-linking and mass spectrometry, and in vivo efficacy in laboratory mating assays.

RESULTS

A targeted chemical library was screened for inhibition of AgTG3 in a fluorescent plate-based assay using its native substrate, plugin. Several inhibitors were identified with IC50 < 10 μM. Preliminary structure-activity relationships within the library support the stereo-specificity and preference for aromatic substituents in the chemical scaffold. Both inhibition of plugin cross-linking and covalent modification of the active site cysteine of AgTG3 were verified. Administration of an AgTG3 inhibitor to A. gambiae males by intrathoracic injection led to a 15% reduction in mating plug transfer in laboratory mating assays.

CONCLUSIONS

A targeted screen has identified chemical inhibitors of A. gambiae transglutaminase 3 (AgTG3). The most potent inhibitors are known inhibitors of human transglutaminase 2, suggesting a common binding pose may exist within the active site of both enzymes. Future efforts to develop additional inhibitors will provide chemical tools to address important biological questions regarding the role of the A. gambiae mating plug. A second use for transglutaminase inhibitors exists for the study of haemolymph coagulation and immune responses to wound healing in insects.

摘要

背景

当前基于媒介的疟疾控制策略受到蚊子生化和行为抗性增加的威胁。需要研究蚊子的免疫和繁殖特性,以寻找新的媒介控制策略的潜在靶点。精浆转谷氨酰胺酶AgTG3使冈比亚按蚊雄蚊的精液凝固,形成“交配栓”,这是雄蚊生殖成功所必需的。AgTG3抑制剂既可以作为冈比亚按蚊生殖生物学的化学探针,也可能推动用于控制蚊虫种群的新型化学绝育剂的开发。

方法

合成了一个靶向3-溴-4,5-二羟基异恶唑抑制剂文库,并在基于平板的荧光测定中筛选其对AgTG3的抑制作用。使用交联和质谱法测试阳性命中物的体外活性,并在实验室交配试验中测试其体内功效。

结果

使用其天然底物“交配栓”在基于平板的荧光测定中筛选靶向化学文库对AgTG3的抑制作用。鉴定出几种IC50<10μM的抑制剂。文库中的初步构效关系支持化学支架中芳香族取代基的立体特异性和偏好性。验证了对“交配栓”交联的抑制以及对AgTG3活性位点半胱氨酸的共价修饰。通过胸腔注射向冈比亚按蚊雄蚊施用AgTG3抑制剂,在实验室交配试验中导致交配栓传递减少15%。

结论

靶向筛选已鉴定出冈比亚按蚊转谷氨酰胺酶3(AgTG3)的化学抑制剂。最有效的抑制剂是已知的人转谷氨酰胺酶2抑制剂,这表明两种酶的活性位点可能存在共同的结合构象。未来开发更多抑制剂的努力将提供化学工具,以解决有关冈比亚按蚊交配栓作用的重要生物学问题。转谷氨酰胺酶抑制剂的第二个用途是研究昆虫血淋巴凝固和对伤口愈合的免疫反应。

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