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果蝇黑素体 85b 气味受体亚基跨膜结构域 3 有助于配体-受体相互作用。

Transmembrane segment 3 of Drosophila melanogaster odorant receptor subunit 85b contributes to ligand-receptor interactions.

机构信息

Department of Molecular and Cellular Pharmacology, University of Miami Miller School of Medicine, Miami, Florida 33101, USA.

出版信息

J Biol Chem. 2010 Apr 16;285(16):11854-62. doi: 10.1074/jbc.M109.058321. Epub 2010 Feb 10.

Abstract

The OR class insect odorant receptors are ligand-gated ion channels comprised of at least one common subunit (OR83b in Drosophila) and at least one putative odorant-binding subunit. However, little else is known about the molecular details of insect OR architecture. For example, nothing is known about how these receptors bind odorants, greatly limiting efforts to develop insect OR-targeted compounds for the control of insects involved in disease propagation and agricultural damage. Here we identify a portion of a Drosophila OR that is involved in odorant activation of the receptor. Using the substituted cysteine accessibility method, we identified residues 146-150 of OR85b, located at the predicted interface between transmembrane segment 3 (TMS3) and extracellular loop 2 (ECL2), as playing a role in odorant (2-heptanone) activation. We found that occupation of the receptor by the competitive antagonist 2-nonanone protected the receptor from methanethiosulfonate action at position 148, placing this region close to the odorant-binding site. In addition, mutations at positions 142 and 143 within TMS3 altered odorant sensitivity. Our results identify the involvement of the extracellular half of TMS3 in Drosophila OR85b in odorant activation of the receptor. This finding can serve as a starting point for future detailed analysis of the molecular basis for odorant recognition by insect ORs, a novel class of ligand-gated channel.

摘要

OR 类昆虫气味受体是配体门控离子通道,由至少一个共同亚基(果蝇中的 OR83b)和至少一个假定的气味结合亚基组成。然而,对于昆虫 OR 结构的分子细节,人们知之甚少。例如,这些受体如何结合气味剂,这极大地限制了开发针对昆虫 OR 的化合物的努力,这些化合物用于控制与疾病传播和农业破坏有关的昆虫。在这里,我们确定了参与受体气味激活的果蝇 OR 的一部分。我们使用取代的半胱氨酸可及性方法,鉴定了 OR85b 中位于跨膜片段 3(TMS3)和细胞外环 2(ECL2)之间的预测界面上的残基 146-150,在气味剂(2-庚酮)激活中发挥作用。我们发现,竞争性拮抗剂 2-壬酮占据受体的位置,可防止甲硫磺酸在位置 148 处作用于受体,将该区域置于接近气味结合位点的位置。此外,TMS3 内位置 142 和 143 的突变改变了气味剂的敏感性。我们的结果表明,TMS3 的细胞外半部分参与了果蝇 OR85b 中受体的气味激活。这一发现可以作为未来昆虫 OR 气味识别分子基础的详细分析的起点,这是一类新型的配体门控通道。

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