FS2。一种曼巴毒液毒素,是l型钙通道的特异性阻滞剂。

Artery Pub Date : 1994-01-01
O Yasuda, S Morimoto, B Jiang, H Kuroda, T Kimura, S Sakakibara, K Fukuo, S Chen, M Tamatani, T Ogihara
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引用次数: 0

摘要

肽FS2是一种曼巴毒液毒素,由60个氨基酸组成,其中3个残基不同于天然l型Ca2+通道阻滞剂calciseptine (CaS)。合成FS2对l型Ca2+通道的生物活性与CaS和尼群地平(一种1,4-二氢吡啶衍生物)的生物活性进行了比较。与CaS类似,FS2在lineweaverbulk图上竞争性地抑制[3H]尼群地平与大鼠脑突触体膜的结合,Kd值为210 nM,与CaS的290 nM相似,但不影响n型Ca2+通道配体omega-[125I]- concontoxin GVIA与细胞膜的结合。预处理A7r5细胞FS2或CaS浓度的10 (8)M和更大的5分钟明显和剂量依赖性降低10(6)米湾K8644-induced免费胞质钙离子浓度增加([Ca2 +] i)的细胞由荧光fura-2 Ca2 +指标,半抑制浓度(IC50)为2.3 x 10(8)和2.7 x 10 (8) M,被类似于nitrendipine的IC50值(4.4 x 10 (8) M)。这些观察表明,FS2与CaS类似,是一种活性的天然l型Ca2+阻滞剂,与1,4-二氢吡啶共享通道上的结合位点。
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FS2. a mamba venom toxin, is a specific blocker of the L-type calcium channels.

The peptide FS2 is a mamba venom toxin, consisting of 60 amino acids, three residues of which are different from those of calciseptine (CaS), a natural L-type Ca2+ channel blocker. The biological activities of synthetic FS2 for L-type Ca2+ channels were determined under comparisons to those of CaS and nitrendipine, a 1,4-dihydropyridine derivative. Similar to CaS, FS2 competitively inhibited the binding of [3H]nitrendipine to rat brain synaptosomal membranes on Lineweaver-Bulk plot, with Kd value of 210 nM, which was similar to that of CaS being 290 nM, but did not affect binding of an N-type Ca2+ channel ligand omega-[125I]-conotoxin GVIA to the membranes. Pretreatment of A7r5 cells with either FS2 or CaS at concentrations of 10(-8) M and greater for 5 min significantly and dose-dependently reduced 10(-6) M Bay K8644-induced increase in the cytosolic free Ca2+ concentration ([Ca2+]i) of the cells determined by the fluorescent Ca2+ indicator fura-2, with the half inhibitory concentrations (IC50) of 2.3 x 10(-8) and 2.7 x 10(-8) M, being similar to that of the IC50 value of nitrendipine (4.4 x 10(-8) M). These observations indicate that FS2, similar to CaS, is an active natural L-type Ca2+ blocker sharing the binding site on the channels with the 1,4-dihydropyridines.

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