Gaudriault G, Zsürger N, Vincent J P
Institut de Pharmacologie Moléculaire et Cellulaire, C.N.R.S. UPR 411, Université de Nice Sophia Antipolis, Valbonne, France.
J Neurochem. 1996 Dec;67(6):2590-8. doi: 10.1046/j.1471-4159.1996.67062590.x.
Radiolabeled analogues of neuromedin N have been prepared by acylation of the alpha, epsilon 1, and epsilon 2 amino groups of [Lys2]neuromedin N (Lys-Lys-Pro-Tyr-Ile-Leu) either with the 125l-labeled Bolton-Hunter reagent or with N-succinimidyl[2,3-3H]propionate. The binding properties of the purified analogues toward newborn mouse brain homogenate or toward membranes of cells transitorily (COS) or permanently (AA1) transfected with the cloned rat brain neurotensin receptor cDNA were evaluated and compared with those of radiolabeled neurotensin. The alpha-modified analogue of [Lys2]neuromedin N behaves exactly like neurotensin in these binding experiments, whereas the epsilon 1- and epsilon 2-modified analogues selectively recognize the fraction of neurotensin binding sites that is sensitive to GTP gamma S. The proportion of neurotensin receptors coupled to GTP binding proteins is approximately 50% in membranes of newborn mouse brain or of AA1 cells that respond to neurotensin by an increase of the intracellular inositol trisphosphate concentration. By contrast, membranes of transitorily transfected COS cells that do not respond to neurotensin exhibit very low levels of GTP-sensitive receptors labeled with the epsilon 1- or epsilon 2-modified analogues. These radiolabeled peptides offer new tools to selectively detect active neurotensin receptors.
已通过用¹²⁵I标记的博尔顿-亨特试剂或N-琥珀酰亚胺基[2,3-³H]丙酸酯对[赖氨酸²]神经降压素N(赖氨酸-赖氨酸-脯氨酸-酪氨酸-异亮氨酸-亮氨酸)的α、ε1和ε2氨基进行酰化反应,制备了神经降压素N的放射性标记类似物。评估了纯化类似物对新生小鼠脑匀浆或对瞬时(COS)或永久(AA1)转染克隆大鼠脑神经降压素受体cDNA的细胞膜的结合特性,并与放射性标记的神经降压素的结合特性进行了比较。在这些结合实验中,[赖氨酸²]神经降压素N的α修饰类似物的行为与神经降压素完全相同,而ε1和ε2修饰类似物则选择性地识别对GTPγS敏感的那部分神经降压素结合位点。在新生小鼠脑或AA1细胞的细胞膜中,与GTP结合蛋白偶联的神经降压素受体比例约为50%,这些细胞通过细胞内三磷酸肌醇浓度的增加对神经降压素作出反应。相比之下,对神经降压素无反应的瞬时转染COS细胞的细胞膜,用ε1或ε2修饰类似物标记的GTP敏感受体水平非常低。这些放射性标记的肽为选择性检测活性神经降压素受体提供了新工具。