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Advanced Identification of Proteins in Uncharacterized Proteomes by Pulsed in Vivo Stable Isotope Labeling-based Mass Spectrometry*

机译:通过基于体内稳定同位素标记的脉冲质谱技术对未表征蛋白质组中的蛋白质进行高级鉴定*

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摘要

Despite progress in the characterization of their genomes, proteomes of several model organisms are often only poorly characterized. This problem is aggravated by the presence of large numbers of expressed sequence tag clones that lack homologues in other species, which makes it difficult to identify new proteins irrespective of whether such molecules are involved in species-specific biological processes. We have used a pulsed stable isotope labeling with amino acids in cell culture (SILAC)-based mass spectrometry method, which is based on the detection of paired peptides after [13C6]lysine incorporation into proteins in vivo, to greatly increase the confidence of protein identification in cross-species database searches. The method was applied to identify nearly 3000 proteins in regenerating tails of the urodele amphibian Notophthalmus viridescens, which possesses outstanding capabilities in the regeneration of complex tissues. We reason that pulsed in vivo SILAC represents a versatile tool to identify new proteins in species for which only limited sequence information exists.
机译:尽管在其基因组的表征方面取得了进展,但几种模式生物的蛋白质组通常仅具有较差的表征。由于存在大量表达的序列标签克隆,而这些克隆在其他物种中缺乏同源性,这使问题变得更加严重,这使得无论这些分子是否参与物种特异性生物学过程,都很难鉴定出新的蛋白质。我们在基于细胞培养(SILAC)的质谱法中使用了氨基酸进行脉冲稳定同位素标记的方法,该方法基于在体内将[13C6]赖氨酸掺入蛋白质后检测配对的肽,从而大大提高了蛋白质的可信度跨物种数据库搜索中的识别。该方法用于鉴定近距离繁殖的尾部两栖野线菌(Notophthalmus viridescens)尾巴中的近3000种蛋白质,该蛋白质在复杂组织的再生中具有出色的能力。我们认为,体内脉冲SILAC代表了一种通用的工具,可用于在仅存在有限序列信息的物种中鉴定新蛋白质。

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