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在8M尿素中通过等电聚焦-电泳联用对多肽链进行滴定曲线分析。

Titration curves of polypeptide chains by combined isoelectric focusing-electrophoresis in 8 M urea.

作者信息

Righetti P G, Krishnamoorthy F, Lapoumeroulie C, Labie D

出版信息

J Chromatogr. 1979 Sep 21;177(2):219-25. doi: 10.1016/s0021-9673(01)96317-4.

Abstract

Titration curves of reduced and alkylated polypeptide chains can be successfully performed in 8 M urea-polyacrylamide gel plates by electrophoresis perpendicular to a stationary stack of focused carrier ampholytes. All buffers and thiol reagents with pK values in the range pH 3--10 should be removed, since their pH-dependent ionization affects the migration and apparent pI values of the protein chains. No blurring of the patterns below pH 4.5 is observed, as usually found in titration curves in the absence of urea, thus allowing the direct titration of Glu and Asp residues. It is not possible by the present technique to titrate any group below pH ca. 3 and above pH ca. 10, due to the lack of suitable carrier ampholytes and to a "flooding" phenomenon, with concomitant identical electrophoretic mobility for all protein species, irrespective of their relative pI values and amino acid composition. The "electrophoretic titration curves" thus obtained were well correlated with the overall amino acid composition of the polypeptide chains analyzed.

摘要

还原和烷基化多肽链的滴定曲线可以通过垂直于固定聚焦载体两性电解质堆叠进行电泳,在8M尿素-聚丙烯酰胺凝胶板中成功完成。所有pK值在pH 3-10范围内的缓冲液和硫醇试剂都应去除,因为它们的pH依赖性电离会影响蛋白质链的迁移和表观pI值。在pH 4.5以下未观察到图案模糊,这与在没有尿素的滴定曲线中通常发现的情况相同,从而允许直接滴定Glu和Asp残基。由于缺乏合适的载体两性电解质以及“淹没”现象,对于所有蛋白质种类,无论其相对pI值和氨基酸组成如何,都具有相同的电泳迁移率,因此用本技术不可能在pH约3以下和pH约10以上滴定任何基团。由此获得的“电泳滴定曲线”与所分析的多肽链的整体氨基酸组成密切相关。

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