The TIM Barrel Architecture Facilitated the Early Evolution of Protein-Mediated Metabolism
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  • 作者:Aaron David Goldman ; Joshua T. Beatty ; Laura F. Landweber
  • 关键词:TIM barrel ; RNA–protein world ; LUCA ; RNA world ; Prebiotic chemistry
  • 刊名:Journal of Molecular Evolution
  • 出版年:2016
  • 出版时间:January 2016
  • 年:2016
  • 卷:82
  • 期:1
  • 页码:17-26
  • 全文大小:3,144 KB
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  • 作者单位:Aaron David Goldman (1)
    Joshua T. Beatty (1)
    Laura F. Landweber (2)

    1. Department of Biology, Oberlin College, Oberlin, OH, 44074, USA
    2. Department of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ, 08544, USA
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Life Sciences
    Cell Biology
    Microbiology
    Plant Sciences
  • 出版者:Springer New York
  • ISSN:1432-1432
文摘
The triosephosphate isomerase (TIM) barrel protein fold is a structurally repetitive architecture that is present in approximately 10 % of all enzymes. It is generally assumed that this ubiquity in modern proteomes reflects an essential historical role in early protein-mediated metabolism. Here, we provide quantitative and comparative analyses to support several hypotheses about the early importance of the TIM barrel architecture. An information theoretical analysis of protein structures supports the hypothesis that the TIM barrel architecture could arise more easily by duplication and recombination compared to other mixed α/β structures. We show that TIM barrel enzymes corresponding to the most taxonomically broad superfamilies also have the broadest range of functions, often aided by metal and nucleotide-derived cofactors that are thought to reflect an earlier stage of metabolic evolution. By comparison to other putatively ancient protein architectures, we find that the functional diversity of TIM barrel proteins cannot be explained simply by their antiquity. Instead, the breadth of TIM barrel functions can be explained, in part, by the incorporation of a broad range of cofactors, a trend that does not appear to be shared by proteins in general. These results support the hypothesis that the simple and functionally general TIM barrel architecture may have arisen early in the evolution of protein biosynthesis and provided an ideal scaffold to facilitate the metabolic transition from ribozymes, peptides, and geochemical catalysts to modern protein enzymes. Keywords TIM barrel RNA–protein world LUCA RNA world Prebiotic chemistry
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