Löbel D, Strotmann J, Jacob M, Breer H
Institute of Physiology, University of Hohenheim, Stuttgart, Germany.
Chem Senses. 2001 Jul;26(6):673-80. doi: 10.1093/chemse/26.6.673.
From a rat olfactory epithelium cDNA library clones encoding a lipocalin were isolated with sequence identity to the previously described salivary-specific alpha-2u globulin and the N-terminal region of mouse odorant-binding proteins OBP-III and OBP-IV. In situ hybridization showed strong expression in nasal glands displaying a pattern equivalent to rat OBP1. Heterologously expressed protein was evaluated for its binding properties using spectroscopic approaches. The recombinant protein interacted with two fluorescent probes, 1-aminoanthracene (1-AMA) and 1,1'-bis(4-anilino-5-naphthalene)-sulfonic acid. 1-AMA binding was competed by several odorants with high affinity. The thermodynamic parameters of the protein-odorant interaction were determined using isothermal titration calorimetry. Due to its nasal expression and odorant-binding characteristics this protein was designated OBP3.
从大鼠嗅觉上皮cDNA文库中分离出编码一种脂质运载蛋白的克隆,该克隆与先前描述的唾液特异性α-2u球蛋白以及小鼠气味结合蛋白OBP-III和OBP-IV的N端区域具有序列同一性。原位杂交显示在鼻腺中有强烈表达,呈现出与大鼠OBP1相当的模式。使用光谱学方法评估了异源表达蛋白的结合特性。重组蛋白与两种荧光探针1-氨基蒽(1-AMA)和1,1'-双(4-苯胺基-5-萘基)磺酸相互作用。几种气味剂以高亲和力竞争1-AMA的结合。使用等温滴定量热法测定了蛋白质-气味剂相互作用的热力学参数。由于其在鼻腔中的表达和气味剂结合特性,该蛋白被命名为OBP3。