Petersen C M
Department of Clinical Immunology, Skejby Hospital, Aarhus.
Dan Med Bull. 1993 Sep;40(4):409-46.
alpha 2-Macroglobulin, a 720 kDa tetramer, and Pregnancy Zone Protein, a 360 kDa dimer, are strongly homologous glycoprotein proteinase inhibitors of human plasma. alpha 2M and PZP monomers contain two regions of decisive functional importance i.e. the bait- and the thiol ester regions. The bait region serves as a substrate to a variety of proteinases, and cleavage in this domain causes a conformational change of the molecule. In addition, PZP forms tetramers when reacted with proteinase. As a result of the conformational change the thiol ester, which is hidden in the native structure, becomes readily accessible, and rapidly reacts with available nucleophiles preferably from the surface of the 'attacking' proteinase. The proteinase is thus covalently linked to alpha 2M/PZP but its active site is not affected. However, due to the structural changes in activated alpha 2M/PZP, bound proteinase is entrapped and its activity towards other than small substrates is sterically hindered. Presentation of receptor recognition sites (maximum four per tetramer) is also a consequence of reaction with proteinase. alpha 2M constitutes a large part of the plasma proteins and in early childhood serum contains as much as 4-5 g/l. Nearly all alpha 2M in the blood is native, since alpha 2M-proteinase complex is subject to rapid receptor-mediated clearance. The serum concentration in adults is about 2 g/l and shows little variation with age. The level is slightly higher in women than in men, and a modest (approximately 20%), possibly oestrogen induced, increase is observed during pregnancy. Sexual hormones, in particular androgens, might also account for the difference between childhood and adult alpha 2M levels. Yet, the reason for the downregulation during adolescence is not firmly established. In contrast to several of its animal homologues, human alpha 2M is not an acute phase protein. The serum level may change during acute and chronic disease, but the change is generally moderate and is not associated with any particular disease. Decreased alpha 2M concentration typically results from enhanced clearance of alpha 2M-proteinase complex and occurs in states of increased proteolytic activity, e.g. pancreatitis. Increased serum alpha 2M is frequently seen in nephrotic conditions and may mirror a change in plasma volume as well as in alpha 2M metabolism. Normal PZP serum levels are > 100 fold lower than those of alpha 2M. Male and female levels are similar in childhood, but unlike alpha 2M, PZP is strongly influenced by hormones.(ABSTRACT TRUNCATED AT 400 WORDS)
α2-巨球蛋白是一种720 kDa的四聚体,妊娠区蛋白是一种360 kDa的二聚体,它们是人类血浆中高度同源的糖蛋白蛋白酶抑制剂。α2M和PZP单体包含两个具有决定性功能重要性的区域,即诱饵区和硫酯区。诱饵区作为多种蛋白酶的底物,该结构域的裂解会导致分子构象改变。此外,PZP与蛋白酶反应时会形成四聚体。构象改变的结果是,原本隐藏在天然结构中的硫酯变得易于接近,并迅速与可用的亲核试剂反应,这些亲核试剂最好来自“攻击”蛋白酶的表面。因此,蛋白酶与α2M/PZP共价连接,但其活性位点不受影响。然而,由于活化的α2M/PZP的结构变化,结合的蛋白酶被截留,并且其对除小底物之外的其他底物的活性受到空间位阻。与蛋白酶反应的另一个结果是呈现受体识别位点(每个四聚体最多四个)。α2M构成血浆蛋白的很大一部分,在儿童早期血清中含量高达4 - 5 g/l。血液中几乎所有的α2M都是天然的,因为α2M - 蛋白酶复合物会被快速的受体介导清除。成年人的血清浓度约为2 g/l,且随年龄变化不大。女性的水平略高于男性,在怀孕期间会观察到适度(约20%)的升高,可能是由雌激素诱导的。性激素,特别是雄激素,也可能是儿童期和成人期α2M水平差异的原因。然而,青春期期间α2M下调的原因尚未完全确定。与它的几种动物同源物不同,人类α2M不是急性期蛋白。血清水平在急性和慢性疾病期间可能会发生变化,但变化通常较为适度,且与任何特定疾病无关。α2M浓度降低通常是由于α2M - 蛋白酶复合物清除增强所致,发生在蛋白水解活性增加的状态下,例如胰腺炎。血清α2M升高在肾病状态下经常出现,可能反映了血浆量以及α2M代谢的变化。正常的PZP血清水平比α2M低100倍以上。儿童期男性和女性的水平相似,但与α2M不同,PZP受到激素的强烈影响。(摘要截取自400字)