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Photo-assisted peptide enrichment in protein complex cross-linking analysis of a model homodimeric protein using mass spectrometry.

机译:使用质谱法对模型同型二聚体蛋白质进行蛋白质复合物交联分析时,光辅助肽富集。

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MS analysis of cross-linked peptides can be used to probe protein contact sites in macromolecular complexes. We have developed a photo-cleavable cross-linker that enhances peptide enrichment, improving the signal-to-noise ratio of the cross-linked peptides in mass spectrometry analysis. This cross-linker utilizes nitro-benzyl alcohol group that can be cleaved by UV irradiation and is stable during the multiple washing steps used for peptide enrichment. The enrichment method utilizes a cross-linker that aids in eliminating contamination resulting from protein-based retrieval systems, and thus, facilitates the identification of cross-linked peptides. Homodimeric pilM protein from Pseudomonas aeruginosa 2192 (pilM) was investigated to test the specificity and experimental conditions. As predicted, the known pair of lysine side chains within 14 A was cross-linked. An unexpected cross-link involving the protein's amino terminus was also detected. This is consistent with the predicted mobility of the amino terminus that may bring the amino groups within 19 A of one another in solution. These technical improvements allow this method to be used for investigating protein-protein interactions in complex biological samples.
机译:交联肽的MS分析可用于探测大分子复合物中的蛋白质接触位点。我们已经开发出一种可光裂解的交联剂,可增强肽的富集度,并改善质谱分析中交联肽的信噪比。该交联剂利用硝基苄基醇基团,该基团可以被紫外线照射裂解,并且在用于肽富集的多个洗涤步骤中稳定。富集方法利用了一种交联剂,该交联剂有助于消除基于蛋白质的检索系统造成的污染,从而有助于鉴定交联的肽。研究了铜绿假单胞菌2192(pilM)的同源二聚体pilM蛋白,以测试其特异性和实验条件。如所预测的,在14 A内已知的一对赖氨酸侧链是交联的。还检测到涉及该蛋白质氨基末端的意外交联。这与氨基末端的预测的迁移率相一致,氨基末端可以将氨基在溶液中彼此转移至19 A之内。这些技术改进使该方法可用于研究复杂生物样品中的蛋白质-蛋白质相互作用。

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