Kleyman T R, Rajagopalan R, Cragoe E J, Erlanger B F, Al-Awqati Q
Am J Physiol. 1986 Jan;250(1 Pt 1):C165-70. doi: 10.1152/ajpcell.1986.250.1.C165.
A new amiloride analogue, "amiloride-caproic acid," was synthesized, coupled to albumin, and used as a hapten to raise anti-amiloride antibodies in rabbits. The antibodies were affinity purified with an amiloride affinity column and characterized. Binding studies using [3H]benzamil showed a dissociation constant of 0.8 nM. Amiloride and amiloride-caproate inhibited [3H]benzamil binding; epsilon-guanidinocaproic acid showed no inhibition. Anti-amiloride antibodies reversed the inhibition by amiloride of sodium transport across toad urinary bladder. Anti-amiloride antibodies and an amiloride affinity column should provide useful tools for the characterization of the epithelial sodium channel.
一种新的氨氯吡咪类似物“氨氯吡咪 - 己酸”被合成出来,与白蛋白偶联,并用作半抗原在兔子体内产生抗氨氯吡咪抗体。这些抗体用氨氯吡咪亲和柱进行亲和纯化并进行表征。使用[3H]苄甲氯铵的结合研究显示解离常数为0.8 nM。氨氯吡咪和氨氯吡咪己酸盐抑制[3H]苄甲氯铵的结合;ε-胍基己酸未显示出抑制作用。抗氨氯吡咪抗体逆转了氨氯吡咪对蟾蜍膀胱钠转运的抑制作用。抗氨氯吡咪抗体和氨氯吡咪亲和柱应为上皮钠通道的表征提供有用的工具。