Hincke M T
Department of Anatomy, University of Ottawa Faculty of Health Sciences, Ontario, Canada.
Anal Biochem. 1988 Apr;170(1):256-63. doi: 10.1016/0003-2697(88)90116-9.
A routine semiquantitative procedure which permits soluble calcium-binding proteins to be detected following their adsorption to nitrocellulose membrane filters by liquid scintillation counting of specifically bound 45Ca is described. Proteins with high affinity for calcium such as calmodulin and troponin can be detected with a detection threshold of about 2 micrograms per 400 microliter. Modifications to decrease this limit are feasible and are discussed. This technique should allow calcium-binding proteins of unknown function to be assayed during their purification. It was necessary to treat solutions containing 45Ca with chelex-100 in order to prevent loss of calcium binding which occurred as the decay product (Sc3+) accumulated, suggesting that all studies utilizing 45Ca as a tracer should evaluate possible interference by this ion.
本文描述了一种常规的半定量方法,该方法通过对特异性结合的45Ca进行液体闪烁计数,在可溶性钙结合蛋白吸附到硝酸纤维素膜过滤器后对其进行检测。对钙具有高亲和力的蛋白质,如钙调蛋白和肌钙蛋白,检测阈值约为每400微升2微克。降低该检测限的改进方法是可行的,并进行了讨论。该技术应能在未知功能的钙结合蛋白纯化过程中对其进行测定。有必要用螯合树脂100处理含45Ca的溶液,以防止由于衰变产物(Sc3+)积累而导致钙结合能力丧失,这表明所有利用45Ca作为示踪剂的研究都应评估该离子可能产生的干扰。