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Degradation artefacts during sample preparation for sodium dodecyl sulphate polyacrylamide gel electrophoresis

机译:十二烷基硫酸钠聚丙烯酰胺凝胶电泳样品制备过程中的降解伪影

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Preparation of samples for sodium dodecyl sulphate polyacrylamide gel electrophoresis routinely involves heating the protein in solution containing detergent and reducing agent for at least two minutes. Here we show that this treatment causes fragmentation of the protein glycogen phosphorylase, whether purified or as a component of a skeletal muscle preparation. The fragments are detected as minor bands on western blots and represent the products of discrete breakage point in the peptide sequence. Protease inhibitors cannot suppress the fragmentation.Such small amounts of immunoreactive fragments may be incorrectly identified on western blots as contaminants that were originally present in the antigen preparation. They may also be a source of ambiguity in studies that search for degradation intermediates during proteolysis.
机译:十二烷基硫酸钠聚丙烯酰胺凝胶电泳样品的制备通常涉及将蛋白质在含有去污剂和还原剂的溶液中加热至少两分钟。在这里,我们显示该处理导致蛋白糖原磷酸化酶的片段化,无论是纯化的还是作为骨骼肌制剂的组分。片段在Western印迹上检测为次要条带,代表肽序列中离散断裂点的产物。蛋白酶抑制剂不能抑制片段化。在免疫印迹中可能会错误地识别出少量的免疫反应片段,这些片段是抗原制剂中最初存在的污染物。它们也可能是在蛋白水解过程中寻找降解中间体的研究中含糊不清的来源。

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