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人类继发性淀粉样变性中淀粉样蛋白A的特征:血清淀粉样蛋白A1的主要沉积

Characterization of amyloid A protein in human secondary amyloidosis: the predominant deposition of serum amyloid A1.

作者信息

Liepnieks J J, Kluve-Beckerman B, Benson M D

机构信息

Richard L. Roudebush Veterans Affairs Medical Center, Indianapolis, IN 46202.

出版信息

Biochim Biophys Acta. 1995 Jan 25;1270(1):81-6. doi: 10.1016/0925-4439(94)00076-3.

Abstract

Serum amyloid A protein (SAA) is the plasma precursor for amyloid A protein (AA), the subunit protein in amyloid deposits of secondary or reactive amyloidosis. Several forms of acute phase SAA have been identified in human plasma. To elucidate whether one of these forms of SAA predominates in the formation of AA amyloid deposits, the amino acid sequence of the subunit protein in six cases of reactive amyloidosis was investigated. Minimal heterogeneity was present at the N-terminus as all samples started with residue 1, 2, or 3 of SAA. The C-terminus, however, was more heterogeneous with the AA protein in each case terminating at multiple sites from residue 58 to 84 of SAA. Since less than 20% of the AA protein in each case contained sequence past residue 67 of SAA, the sequence and recovery of tryptic peptides containing residues 52, 57, and 60 where human SAA1 and 2 differ was used to determine the relative amounts of SAA1 and 2 present. One sample contained only SAA1 sequence, four contained approx. 11% or less of SAA2 sequence, and the sixth contained 24-33% of SAA2 sequence. Thus, while five of the six AA samples contained both SAA1 and 2, the predominant form in all cases was SAA1. In three of the six cases, the protein defensin was isolated along with the AA protein from the fibrils. This may suggest neutrophil involvement in SAA processing to AA fibrils.

摘要

血清淀粉样蛋白A(SAA)是淀粉样蛋白A(AA)的血浆前体,AA是继发性或反应性淀粉样变性淀粉样沉积物中的亚基蛋白。已在人血浆中鉴定出几种急性期SAA形式。为了阐明这些SAA形式中的一种是否在AA淀粉样沉积物的形成中占主导地位,研究了6例反应性淀粉样变性患者亚基蛋白的氨基酸序列。N端存在最小异质性,因为所有样本均以SAA的第1、2或3位残基开始。然而,C端的异质性更大,每种情况下的AA蛋白在SAA的第58至84位残基的多个位点处终止。由于每种情况下不到20%的AA蛋白包含超过SAA第67位残基的序列,因此使用包含人SAA1和2不同的第52、57和60位残基的胰蛋白酶肽的序列和回收率来确定存在的SAA1和2的相对量。一个样本仅包含SAA1序列,四个样本包含约11%或更少的SAA2序列,第六个样本包含24 - 33%的SAA2序列。因此,虽然六个AA样本中的五个同时包含SAA1和2,但所有情况下的主要形式都是SAA1。在六个病例中的三个病例中,从纤维中分离出了与AA蛋白一起的防御素蛋白。这可能表明中性粒细胞参与了SAA加工成AA纤维的过程。

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