Grove A, Tomich J M, Montal M
Department of Biology, University of California San Diego, La Jolla 92093-0319.
Proc Natl Acad Sci U S A. 1991 Aug 1;88(15):6418-22. doi: 10.1073/pnas.88.15.6418.
A protein that imitates the sequence of a highly conserved segment predicted to line the pore of dihydropyridine-sensitive L-type calcium channels was designed and synthesized. Single-channel conductance properties were studied in planar lipid bilayers. The synthetic protein emulates the ionic conductance, ionic selectivity, and pharmacological properties of the authentic calcium channel, including the stereospecific action of agonist and antagonist enantiomers of the dihydropyridine BayK 8644. The identified sequence is identical in L-type calcium channels from skeletal muscle and isoforms of cardiac muscle, brain, and aorta. It is plausible that this structural motif represents the molecular blueprint for the pore-forming structure of voltage-gated calcium channels.
设计并合成了一种蛋白质,该蛋白质模拟了预测位于二氢吡啶敏感性L型钙通道孔道的高度保守片段的序列。在平面脂质双分子层中研究了单通道电导特性。合成蛋白模拟了真实钙通道的离子电导、离子选择性和药理学特性,包括二氢吡啶BayK 8644激动剂和拮抗剂对映体的立体特异性作用。所鉴定的序列在骨骼肌以及心肌、脑和主动脉的亚型的L型钙通道中是相同的。这种结构基序可能代表了电压门控钙通道孔形成结构的分子蓝图。