Marks A R, Tempst P, Chadwick C C, Riviere L, Fleischer S, Nadal-Ginard B
Laboratory of Molecular and Cellular Cardiology, Children's Hospital, Boston, Massachusetts.
J Biol Chem. 1990 Dec 5;265(34):20719-22.
Inositol 1,4,5-trisphosphate (InsP3) mediates smooth muscle contraction by mobilizing intracellular calcium release. In this study we provide a direct comparison of the smooth muscle and brain InsP3 receptors in terms of InsP3 binding and primary structure. The KD for InsP3 binding for both receptors was found to be essentially the same. Sequences from 11 bovine smooth muscle receptor tryptic peptides (120 amino acids) were identified in the mouse brain receptor with two substitutions attributable to species differences. A cDNA (approximately 1-kilobase) encoding a portion of the mouse smooth muscle InsP3 receptor was cloned and found to be identical to that reported for the brain receptor. This cDNA was used as a probe to demonstrate that the approximately 10-kilobase InsP3 receptor mRNA is detected in brain, smooth muscle, heart, liver, and kidney but was not detected in skeletal muscle or skin.
肌醇1,4,5 -三磷酸(InsP3)通过动员细胞内钙释放来介导平滑肌收缩。在本研究中,我们就InsP3结合和一级结构对平滑肌和脑InsP3受体进行了直接比较。发现两种受体对InsP3结合的解离常数(KD)基本相同。在小鼠脑受体中鉴定出了11个牛平滑肌受体胰蛋白酶肽段(120个氨基酸)的序列,有两个替换归因于物种差异。克隆了编码小鼠平滑肌InsP3受体一部分的cDNA(约1千碱基),发现其与报道的脑受体的cDNA相同。该cDNA用作探针,证明在脑、平滑肌、心脏、肝脏和肾脏中检测到约10千碱基的InsP3受体mRNA,但在骨骼肌或皮肤中未检测到。