ACS Chemical Biology 2015-08-21

A Clickable Aminooxy Probe for Monitoring Cellular ADP-Ribosylation.

Rory K Morgan, Michael S Cohen

文献索引：ACS Chem. Biol. 10 , 1778-84, (2015)

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摘要

ADP-ribosylation is essential for cell function, yet there is a dearth of methods for detecting this post-translational modification in cells. Here, we describe a clickable aminooxy alkyne (AO-alkyne) probe that can detect cellular ADP-ribosylation on acidic amino acids following Cu-catalyzed conjugation to an azide-containing reporter. Using AO-alkyne, we show that PARP10 and PARP11 are auto-ADP-ribosylated in cells. We also demonstrate that AO-alkyne can be used to monitor stimulus-induced ADP-ribosylation in cells. Functional studies using AO-alkyne support a previously unknown mechanism for ADP-ribosylation on acidic amino acids, wherein a glutamate or aspartate at the initial C1'-position of ADP-ribose transfers to the C2' position. This new mechanism for ADP-ribosylation has important implications for how glutamyl/aspartyl-ADP-ribose is recognized by proteins in cells.

相关化合物

  • 咪唑
  • 三氟乙酸五氟苯酯
  • 叔丁氧羰基氨氧基乙...
  • 4-羟乙基哌嗪乙磺酸
  • 苯甲脒
  • 苄磺酰氟
  • 甘油
  • 磷酸二氢钾
  • 酸性红52
  • 氯霉素

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