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蛋白质经等电聚焦后进行电泳,通过酶谱法和免疫固定法观察其滴定曲线。

Isoelectric focusing following by electrophoresis of proteins for visualizing their titration curves by zymogram and immunofixation.

作者信息

Gianazza E, Gelfi C, Righetti P G

出版信息

J Biochem Biophys Methods. 1980 Aug;3(2):65-75. doi: 10.1016/0165-022x(80)90029-9.

Abstract

After isoelectric focusing followed by electrophoresis at right angles in the same gel slab, it is possible to visualize the titration curve of proteins by zymograms or immunofixation even of an unpurified sample. This information can be very useful for the selection of the proper purification strategy by charge-dependent methods, e.g. ion-exchange chromatography, zone and disc electrophoresis and isotachophoresis. The titration curve also gives information on the stability of the protein as a function of the prevailing pH of the medium, in the pH 3-10 range. A region of instability is found for most proteins in acidic conditions, below pH 4.5, while most proteins are stable in the alkaline pH region, at least up to pH 10. The best method for developing zymograms and immunoprints appears to pH 10. The best method for developing zymograms and immunoprints appears to be the 'sandwich technique', by which a thin agarose slab, cast on an hydrophilic polyester sheet, and impregnated with appropriate reagents, is left in contact with a polyacrylamide gel thin layer used to generate the titration curves.

摘要

在等电聚焦之后,于同一凝胶板中进行直角电泳,即使对于未纯化的样品,也能够通过酶谱或免疫固定来观察蛋白质的滴定曲线。该信息对于通过基于电荷的方法(例如离子交换色谱法、区带电泳和圆盘电泳以及等速电泳)选择合适的纯化策略非常有用。滴定曲线还给出了在pH 3 - 10范围内,蛋白质稳定性随介质中主要pH值变化的信息。在酸性条件下,pH值低于4.5时,大多数蛋白质存在不稳定区域,而大多数蛋白质在碱性pH区域是稳定的,至少在pH值达到10时是稳定的。显影酶谱和免疫印记的最佳方法似乎是“三明治技术”,即把浇铸在亲水性聚酯片上并浸渍有适当试剂的薄琼脂糖板与用于生成滴定曲线的聚丙烯酰胺凝胶薄层接触。

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