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Linking Protein Mass with Function via Organismal Massome Networks

机译:通过有机体Massome Network将蛋白质与功能连接

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With the human genome sequenced, attention has been shifting to proteins and their function. Several technologies including mass spectrometry and gel electrophoresis have traditionally been used to study proteins. These technologies rely on proteins' masses to characterize and/or identify them. Once identified, the discovered proteins' are often analyzed for their functional relevance. In this paper, we present an alternative approach to studying protein function directly, based on protein mass. By analyzing proteins with similar mass ranges (bins), we discovered that certain biological functions are associated with specific mass bins more frequently than would be expected by chance. Biological functional classes found in this manner could be seen across the three examined organisms: human, worm and fly. We found no sequence-based homology across significant mass-function proteins in the three different organisms. This investigation leads to useful property that the mass-based biological functional classes are preserved across the organisms. Thus, this paper describes a potential constraint for evolution of similar function based on mass constraints. Finally, this work yields a roadmap for experimental design for functional exploration of proteomes in mass-based technologies such as gel electrophoresis and mass spectrometry.
机译:随着人类基因组测序,注意力已经转移到蛋白质和它们的功能。传统上用于研究蛋白质,包括质谱和凝胶电泳等几种技术。这些技术依赖于蛋白质的群众来表征和/或识别它们。一旦鉴定,发现发现的蛋白质“通常用于其功能相关性。本文基于蛋白质,我们提出了一种直接研究蛋白质功能的替代方法。通过分析具有类似质量范围(箱)的蛋白质,我们发现某些生物学功能与特定的质量箱更频繁地相关,而不是偶然的机会。在三次检查的生物体中可以看到以这种方式发现的生物功能类:人类,蠕虫和飞行。我们在三种不同的生物体中发现了在显着的质量功能蛋白上没有基于序列的同源性。该研究导致有用的性质,即在生物体中保存了基于群众的生物功能类。因此,本文介绍了基于质量约束的类似功能的演变的潜在约束。最后,这项工作产生了一种用于实验设计的路线图,用于蛋白质谱中的蛋白质谱中的凝胶电泳和质谱法的功能探测。

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