Gaillard Isabelle, Rouquier Sylvie, Pin Jean-Philippe, Mollard Patrice, Richard Sylvain, Barnabé Cécile, Demaille Jacques, Giorgi Dominique
IGH, CNRS UPR 1142, rue de la Cardonille, 34396 Montpellier cedex 5, France.
Eur J Neurosci. 2002 Feb;15(3):409-18. doi: 10.1046/j.0953-816x.2001.01871.x.
The sense of smell is mediated by the initiation of action potential in olfactory sensory neurons during odor stimulation. However, little is known about odorant-olfactory receptor (OR) recognition mechanisms. In the present work, we identified the structural motifs of odorant molecules required to activate mouse OR912-93 by detection of the odorant response using calcium measurement in cells transfected with OR and G(alpha)q and G(alpha)15 proteins. The use of sets of odorants led to the identification of ketones with an aliphatic carbon chain length >or= four carbon atoms and a carbonyl group preferentially located in position C2 or C3. The threshold of detection of these odorants is as low as 10(-6)-10(-8)m. No other odorant ligand, out of 70 representatives of the odorant world, was active. The human ortholog of OR912-93 is not functional, suggesting that apart from a stop-mutation located at the 5'-end that was corrected in the construct, it incurred other deleterious mutations during evolution.
嗅觉是由气味刺激期间嗅觉感觉神经元中动作电位的启动介导的。然而,关于气味剂 - 嗅觉受体(OR)识别机制知之甚少。在本研究中,我们通过在转染了OR以及G(α)q和G(α)15蛋白的细胞中使用钙测量检测气味剂反应,确定了激活小鼠OR912 - 93所需的气味剂分子的结构基序。使用一系列气味剂导致鉴定出具有脂肪族碳链长度≥四个碳原子且羰基优先位于C2或C3位置的酮类。这些气味剂的检测阈值低至10(-6)-10(-8)m。在70种气味剂代表中,没有其他气味剂配体具有活性。OR912 - 93的人类直系同源物无功能,这表明除了构建体中校正的位于5'端的终止突变外,它在进化过程中还发生了其他有害突变。