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PARPs and ADP-ribosylation: Deciphering the complexity with molecular tools. | LitMetric

PARPs and ADP-ribosylation: Deciphering the complexity with molecular tools.

Mol Cell

Department of Biochemistry and Molecular Biology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD 21205, USA; Department of Molecular Biology and Genetics, Department of Oncology, and Department of Genetic Medicine, School of Medicine, Johns Hopkins University, Baltimore, MD 21205, USA. Electronic address:

Published: May 2023

AI Article Synopsis

  • PARPs are enzymes that catalyze ADP-ribosylation, a key process involved in DNA repair, immune response, and more.
  • Advancements in chemical biology have allowed researchers to analyze ADP-ribosylated molecules and enzymes on a large scale, enabling the creation of specific inhibitors and therapeutic options.
  • Innovative tools like genetically encoded reporters and improved immunoassays are enhancing the real-time monitoring and understanding of ADP-ribosylation's role in health and disease.

Article Abstract

PARPs catalyze ADP-ribosylation-a post-translational modification that plays crucial roles in biological processes, including DNA repair, transcription, immune regulation, and condensate formation. ADP-ribosylation can be added to a wide range of amino acids with varying lengths and chemical structures, making it a complex and diverse modification. Despite this complexity, significant progress has been made in developing chemical biology methods to analyze ADP-ribosylated molecules and their binding proteins on a proteome-wide scale. Additionally, high-throughput assays have been developed to measure the activity of enzymes that add or remove ADP-ribosylation, leading to the development of inhibitors and new avenues for therapy. Real-time monitoring of ADP-ribosylation dynamics can be achieved using genetically encoded reporters, and next-generation detection reagents have improved the precision of immunoassays for specific forms of ADP-ribosylation. Further development and refinement of these tools will continue to advance our understanding of the functions and mechanisms of ADP-ribosylation in health and disease.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10202152PMC
http://dx.doi.org/10.1016/j.molcel.2023.04.009DOI Listing

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