Kalia K, Chandra S V, Viswanathan P N
Acta Pharmacol Toxicol (Copenh). 1984 Apr;54(4):247-52. doi: 10.1111/j.1600-0773.1984.tb01925.x.
Studies were undertaken to investigate the 54Mn binding protein in rat serum, liver and brain. Equilibrium dialysis pattern in three biological media with 54Mn against distilled water showed a rectangular hyperbola after 24 hr dialysis. 54Mn in the bag was in the non-dialysable form, presumably bound to protein. Gel filtration studies with 54Mn bound protein showed that 54Mn had a specific carrier protein, which was identical for all the three biological media tested. The electrophorogram of concentrated 54Mn protein with Comassie blue stain for protein and PAS stain for glycoprotein showed a single band with an equal RF value clearly indicating the glycoprotein nature of 54Mn binding protein. Sulphydryl groups were absent and it had molecular weight of 6.3 X 10(4) dalton.
开展了多项研究以调查大鼠血清、肝脏和大脑中的54Mn结合蛋白。在三种生物介质中用54Mn对蒸馏水进行平衡透析,24小时透析后呈现出矩形双曲线。袋中的54Mn处于不可透析形式,推测与蛋白质结合。对54Mn结合蛋白进行凝胶过滤研究表明,54Mn有一个特定的载体蛋白,在所测试的所有三种生物介质中都是相同的。用考马斯亮蓝染蛋白和过碘酸希夫试剂染糖蛋白对浓缩的54Mn蛋白进行电泳图谱分析,显示出一条单一的条带,其Rf值相等,清楚地表明了54Mn结合蛋白的糖蛋白性质。不存在巯基,其分子量为6.3×10⁴道尔顿。