Fiedler-Nagy C, Rowley G R, Coffey J W, Miller O N
Br J Haematol. 1975 Nov;31(3):311-21. doi: 10.1111/j.1365-2141.1975.tb00862.x.
When dialysed rat serum which contains a single, low molecular weight binder for vitamin B12, rat transcobalamin II (rat TC-II), was labelled in vitro with 57Co-vitamin B12 and then incubated at 30 degrees C (pH 7-5) with vesicles of highly purified plasma membranes separated from microsomal fractions of rat liver by density gradient centrifugation, the 57Co-vitamin B12-rat TC-II complex bound to high affinity sites on the vesicles via a specific (binding after correction for 'non-specific' binding in the presence of a large excess of the non-radioactive complex), saturable, and reversible interaction. The apparent affinity constant for the binding reaction was 5-5 X 10(9) M-1. Using the same incubation conditions, free vitamin B12 also bound to the vesicles of plasma membranes via a specific, saturable, but apparently irreversible interaction. Preincubation of the membranes with free vitamin B12 did not interfere with the subsequent binding of the vitamin B12-rat TC-II complex to the membranes; however, preincubation with the vitamin B12-rat TC-II complex did interfere, to some extent, with the subsequent binding of free vitamin B12. Dialysed rat serum, perhaps the free rat TC-II in the dialysed serum, also inhibited the binding of the vitamin B12-rat TC-II complex to the plasma membranes. The relationship of the binding sites identified in this report to the absorption of vitamin B12 by rat liver, and thus their physiological significance remains unknown until further work is done, perhaps using intact hepatocytes.
当含有单一低分子量维生素B12结合蛋白——大鼠转钴胺素II(大鼠TC-II)的透析大鼠血清在体外与57Co-维生素B12进行标记,然后在30℃(pH 7.5)下与通过密度梯度离心从大鼠肝脏微粒体部分分离出的高度纯化的质膜囊泡一起孵育时,57Co-维生素B12-大鼠TC-II复合物通过一种特异性(在存在大量非放射性复合物时校正“非特异性”结合后的结合)、可饱和且可逆的相互作用与囊泡上的高亲和力位点结合。结合反应的表观亲和常数为5.5×109 M-1。在相同的孵育条件下,游离维生素B12也通过一种特异性、可饱和但明显不可逆的相互作用与质膜囊泡结合。用游离维生素B12对膜进行预孵育并不干扰随后维生素B12-大鼠TC-II复合物与膜的结合;然而,用维生素B12-大鼠TC-II复合物进行预孵育在一定程度上确实会干扰随后游离维生素B12的结合。透析大鼠血清,可能是透析血清中的游离大鼠TC-II,也抑制了维生素B12-大鼠TC-II复合物与质膜的结合。本报告中鉴定的结合位点与大鼠肝脏对维生素B12的吸收之间的关系,以及因此它们的生理意义,在进一步开展工作(可能使用完整的肝细胞)之前仍然未知。