The Many Faces of Histidine Triad Nucleotide Binding Protein 1 (HINT1)

Maxwell Dillenburg, Jacob Smith, Carston R. Wagner

Research output: Contribution to journalReview articlepeer-review

2 Scopus citations

Abstract

The histidine triad nucleotide binding protein 1 (HINT1) is a nucleoside phosphoramidase that has garnered interest due to its widespread expression and participation in a broad range of biological processes. Herein, we discuss the role of HINT1 as a regulator of several CNS functions, tumor suppressor, and mast cell activator via its interactions with multiple G-protein-coupled receptors and transcription factors. Importantly, altered HINT1 expression and mutation are connected to the progression of multiple disease states, including several neuropsychiatric disorders, peripheral neuropathy, and tumorigenesis. Additionally, due to its involvement in the activation of several clinically used phosphoramidate prodrugs, tremendous efforts have been made to better understand the interactions behind nucleoside binding and phosphoramidate hydrolysis by HINT1. We detail the substrate specificity and catalytic mechanism of HINT1 hydrolysis, while highlighting the structural biology behind these efforts. The aim of this review is to summarize the multitude of biological and pharmacological functions in which HINT1 participates while addressing the areas of need for future research.

Original languageEnglish (US)
Pages (from-to)1310-1322
Number of pages13
JournalACS Pharmacology and Translational Science
Volume6
Issue number10
DOIs
StatePublished - Oct 13 2023

Bibliographical note

Publisher Copyright:
© 2023 American Chemical Society.

Keywords

  • ProTide
  • amino acyl t-RNA synthetase
  • histidine triad nucleotide binding protein
  • inherited peripheral neuopathy
  • opioid tolerance
  • pain
  • pronucleotide

PubMed: MeSH publication types

  • Journal Article
  • Review

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