首页> 外文OA文献 >Trypsin-induced activation of the thiol esters in α2-macroglobulin generates a short-lived intermediate (‘nascent’ α2M) that can react rapidly to incorporate not only methylamine or putrescine but also proteins lacking proteinase activity

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Trypsin-induced activation of the thiol esters in α2-macroglobulin generates a short-lived intermediate (‘nascent’ α2M) that can react rapidly to incorporate not only methylamine or putrescine but also proteins lacking proteinase activity

机译：胰蛋白酶诱导的α2-巨球蛋白中硫醇酯的活化产生短寿命的中间体（“新生”α2M），该中间体可以快速反应以不仅掺入甲胺或腐胺，还可以掺入缺乏蛋白酶活性的蛋白质

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Sottrup-Jensen Lars; Petersen Torben E.; Magnusson Staffan;
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年度 1981
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外文文献

1. Binding of proteinases to human α2-macroglobulin with its thioester bonds cleaved by methylamine in the presence of a thiol-group-cyanylating reagent [J] . I Bj?rk The biochemical journal . 1985,第2期

机译：在硫醇基氰基化试剂存在下，蛋白酶与人α2-巨球蛋白的硫酯键被甲胺裂解
2. Binding of proteinases to human α2-macroglobulin with its thioester bonds cleaved by methylamine in the presence of a thiol-group-cyanylating reagent [J] . I Bj?rk The biochemical journal . 1985,第2期

机译：在硫醇基氰基化试剂存在下，蛋白酶与人α2-巨球蛋白的硫酯键被甲胺裂解
3. Efficient degradation in vitro of all intermediate filament subunit proteins by the Ca2+-activated neutral thiol proteinase from Ehrlich ascites tumor cells and porcine kidney [J] . Constantin E. Vorgias, Peter Traub Bioscience Reports . 1986,第1期

机译：Ca2 +活化的中性硫醇蛋白酶从Ehrlich腹水肿瘤细胞和猪肾中体外降解所有中间丝亚基蛋白
4. Binding of proteinases to human alpha 2-macroglobulin with its thioester bonds cleaved by methylamine in the presence of a thiol-group-cyanylating reagent. [O] . I Björk 1985

机译：在硫醇基-氰基化试剂的存在下蛋白酶与人α2-巨球蛋白的硫酯键被甲胺裂解。
5. A thiol-ester in α2-macroglobulin cleaved during proteinase complex formation [O] . Sottrup-Jensen Lars, Petersen Torben E., Magnusson Staffan 1980

机译：蛋白酶复合物形成过程中裂解的α2-巨球蛋白中的硫醇酯

Trypsin-induced activation of the thiol esters in α2-macroglobulin generates a short-lived intermediate (‘nascent’ α2M) that can react rapidly to incorporate not only methylamine or putrescine but also proteins lacking proteinase activity

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