Chemical Synthesis of Diubiquitin‐Based Photoaffinity Probes for Selectively Profiling Ubiquitin‐Binding Proteins

  • Jun Liang
    Hefei National Laboratory for Physical Sciences at the Microscale University of Science and University of Science and Technology of China Hefei 230026 China
  • Lin Zhang
    MOE Key Laboratory of Bioinformatics, Tsinghua-Peking Joint Center for Life Sciences, School of Life Sciences Tsinghua University Beijing 100084 China
  • Xiang‐Long Tan
    Department of Chemistry Tsinghua University Beijing 100084 China
  • Yun‐Kun Qi
    Department of Chemistry Tsinghua University Beijing 100084 China
  • Shan Feng
    MOE Key Laboratory of Bioinformatics, Tsinghua-Peking Joint Center for Life Sciences, School of Life Sciences Tsinghua University Beijing 100084 China
  • Haiteng Deng
    MOE Key Laboratory of Bioinformatics, Tsinghua-Peking Joint Center for Life Sciences, School of Life Sciences Tsinghua University Beijing 100084 China
  • Yijing Yan
    Hefei National Laboratory for Physical Sciences at the Microscale University of Science and University of Science and Technology of China Hefei 230026 China
  • Ji‐Shen Zheng
    Hefei National Laboratory for Physical Sciences at the Microscale University of Science and University of Science and Technology of China Hefei 230026 China
  • Lei Liu
    Department of Chemistry Tsinghua University Beijing 100084 China
  • Chang‐Lin Tian
    Hefei National Laboratory for Physical Sciences at the Microscale University of Science and University of Science and Technology of China Hefei 230026 China

書誌事項

公開日
2017-02
権利情報
  • http://onlinelibrary.wiley.com/termsAndConditions#vor
DOI
  • 10.1002/anie.201611659
公開者
Wiley

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説明

<jats:title>Abstract</jats:title><jats:p>Biochemical studies of cellular processes involving polyubiquitin have gained increasing attention. More tools are needed to identify ubiquitin (Ub)‐binding proteins. We report diazirine‐based photoaffinity probes that can capture Ub‐binding proteins in cell lysates, and show that diazirines are preferable to aryl azides as the photo‐crosslinking group, since they decrease non‐selective capture. Photoaffinity probes containing at least two Ub units were required to effectively capture Ub‐binding proteins. Different capture selectivity was observed for probes containing diubiquitin moieties with different types of linkages, thus indicating the potential to develop linkage‐dependent probes for selectively profiling Ub‐binding proteins under various cellular conditions.</jats:p>

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