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C1抑制剂铰链区突变通过不同机制导致功能障碍。

C1 inhibitor hinge region mutations produce dysfunction by different mechanisms.

作者信息

Davis A E, Aulak K, Parad R B, Stecklein H P, Eldering E, Hack C E, Kramer J, Strunk R C, Bissler J, Rosen F S

机构信息

Division of Nephrology, Children's Hospital Research Foundation, Cincinnati, Ohio.

出版信息

Nat Genet. 1992 Aug;1(5):354-8. doi: 10.1038/ng0892-354.

Abstract

Heterozygosity for a mutant dysfunctional C1 inhibitor protein, a member of the serine proteinase inhibitor (serpin) superfamily, results in type II hereditary angioneurotic oedema. We identified a "hinge" region mutation in C1 inhibitor with a Val to Glu replacement at P14 Val-432. Recombinant C1 inhibitors P10 Ala-->Thr and P14Val-->Glu did not form stable complexes with fluid phase C1s or kallikrein. The P14 Val-->Glu mutant, however, was cleaved to a 96K form by C1s, while the P10 Ala-->Thr mutant was not. The recombinant P10 mutant also did not complex with C1s, kallikrein or beta-factor Xlla-Sepharose. The two mutations, therefore, result in dysfunction by different mechanisms: in one (P14 Val-->Glu), the inhibitor is converted to a substrate, while in the other (P10 Ala-->Thr), interaction with target protease is blocked.

摘要

突变的功能失调性C1抑制蛋白(丝氨酸蛋白酶抑制剂(serpin)超家族的成员)杂合子会导致II型遗传性血管性水肿。我们在C1抑制剂中鉴定出一个“铰链”区突变,在P14 Val-432处发生了缬氨酸到谷氨酸的替换。重组C1抑制剂P10 Ala→Thr和P14Val→Glu不能与液相C1s或激肽释放酶形成稳定的复合物。然而,P14 Val→Glu突变体被C1s切割成96K形式,而P10 Ala→Thr突变体则不会。重组P10突变体也不能与C1s、激肽释放酶或β-因子Xlla-琼脂糖形成复合物。因此,这两个突变通过不同机制导致功能失调:在一个突变(P14 Val→Glu)中,抑制剂转化为底物,而在另一个突变(P10 Ala→Thr)中,与靶蛋白酶的相互作用被阻断。

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