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下一代神经肽Y受体小分子激动剂可抑制蚊子叮咬行为。

Next Generation Neuropeptide Y Receptor Small Molecule Agonists Inhibit Mosquito Biting Behavior.

作者信息

Zeledon Emely V, Baxt Leigh A, Khan Tanweer A, Michino Mayako, Miller Michael, Huggins David J, Jiang Caroline S, Vosshall Leslie B, Duvall Laura B

机构信息

Laboratory of Neurogenetics and Behavior, The Rockefeller University, New York NY 10065, USA.

Howard Hughes Medical Institute, New York NY 10065, USA.

出版信息

bioRxiv. 2024 Mar 5:2024.02.28.582529. doi: 10.1101/2024.02.28.582529.

Abstract

Female mosquitoes can spread disease-causing pathogens when they bite humans to obtain blood nutrients required for egg production. Following a complete blood meal, host-seeking is suppressed until eggs are laid. Neuropeptide Y-like Receptor 7 (NPYLR7) plays a role in endogenous host-seeking suppression and previous work identified small molecule NPYLR7 agonists that suppress host-seeking and blood feeding when fed to mosquitoes at high micromolar doses. Using structure activity relationship analysis and structure-guided design we synthesized 128 compounds with similarity to known NPYLR7 agonists. Although potency (EC) was not strictly predictive of effect, we identified 3 compounds that suppressed blood feeding from a live host when fed to mosquitoes at a 1 μM dose, a 100-fold improvement over the original reference compound. Exogenous activation of NPYLR7 represents an innovative vector control strategy to block mosquito biting behavior and prevent mosquito/human host interactions that lead to pathogen transmission.

摘要

雌性蚊子在叮咬人类以获取产卵所需的血液营养时,能够传播致病病原体。在饱餐一顿血液后,寻找宿主的行为会受到抑制,直到产卵。神经肽Y样受体7(NPYLR7)在内源性寻找宿主行为抑制中发挥作用,先前的研究确定了小分子NPYLR7激动剂,当以高微摩尔剂量喂给蚊子时,这些激动剂会抑制寻找宿主和吸血行为。利用构效关系分析和结构导向设计,我们合成了128种与已知NPYLR7激动剂相似的化合物。尽管效力(EC)并不能严格预测效果,但我们确定了3种化合物,当以1μM的剂量喂给蚊子时,它们能抑制从活体宿主获取血液,比原始参考化合物有100倍的改善。NPYLR7的外源性激活代表了一种创新的病媒控制策略,可阻止蚊子的叮咬行为,并防止导致病原体传播的蚊子/人类宿主相互作用。

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