Xu W, Denison H, Hale C C, Gatto C, Milanick M A
Department of Physiology, School of Medicine, University of Missouri-Columbia 65212, USA.
Arch Biochem Biophys. 1997 May 15;341(2):273-9. doi: 10.1006/abbi.1997.9954.
The peptides XIP (RRLLFYKYVYKRYRAGKQRG) and C28R2 (LRRGQILWFRGLNRIQTQIRVVKAFRSS) correspond to the autoinhibitory domains of the Na-Ca exchanger and the plasma membrane Ca pump, respectively. An increase of ionic strength reduced the inhibition of exchange activity by XIP and C28R2, consistent with an important role for electrostatic interactions. Sulfosuccinimidyl acetate (SNA)-modified XIP did not inhibit Na-Ca exchange. Because SNA modifies lysines, we conclude that at least one of the positive charges at the XIP lysine positions (7, 11, or 17) is important for inhibition. 2CK-XIP (RRLLFYRYVYRCYCAGRQKG) has cysteines at 12 and 14 and only one lysine (at 19).2CK-XIP inhibited Na-Ca exchange; thus positive charges at 12 and 14 are not essential. SNA-modified 2CK-XIP did not inhibit; thus a positive charge at 19 is important. Iodoacetic acid-modified 2CK-XIP inhibits the Na-Ca exchanger but not the PM Ca pump. These results show that the structural determinants for inhibition of the Na-Ca exchanger and the PM Ca pump are different, that positive charges at 7, 11, or 17 (or some combination) are more important than positive charges at 12 and 14 for inhibition by XIP of the Na-Ca exchanger.
肽XIP(RRLLFYKYVYKRYRAGKQRG)和C28R2(LRRGQILWFRGLNRIQTQIRVVKAFRSS)分别对应于钠钙交换体和质膜钙泵的自身抑制结构域。离子强度的增加降低了XIP和C28R2对交换活性的抑制作用,这与静电相互作用的重要作用一致。磺基琥珀酰亚胺乙酸酯(SNA)修饰的XIP不抑制钠钙交换。由于SNA修饰赖氨酸,我们得出结论,XIP赖氨酸位置(7、11或17)的至少一个正电荷对抑制作用很重要。2CK-XIP(RRLLFYRYVYRCYCAGRQKG)在12和14位有半胱氨酸,只有一个赖氨酸(在19位)。2CK-XIP抑制钠钙交换;因此12和14位的正电荷不是必需的。SNA修饰的2CK-XIP不抑制;因此19位的正电荷很重要。碘乙酸修饰的2CK-XIP抑制钠钙交换体但不抑制质膜钙泵。这些结果表明,抑制钠钙交换体和质膜钙泵的结构决定因素不同,对于XIP抑制钠钙交换体而言,7、11或17位的正电荷(或某些组合)比12和14位的正电荷更重要。