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NAD Analogs in Aid of Chemical Biology and Medicinal Chemistry

Nicotinamide adenine dinucleotide (NAD) serves as an essential redox co-factor and mediator of multiple biological processes. Besides its well-established role in electron transfer reactions, NAD serves as a substrate for other biotransformations, which, at the molecular level, can be classified as...

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Autores principales: Depaix, Anais, Kowalska, Joanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6891637/
https://www.ncbi.nlm.nih.gov/pubmed/31752261
http://dx.doi.org/10.3390/molecules24224187
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author Depaix, Anais
Kowalska, Joanna
author_facet Depaix, Anais
Kowalska, Joanna
author_sort Depaix, Anais
collection PubMed
description Nicotinamide adenine dinucleotide (NAD) serves as an essential redox co-factor and mediator of multiple biological processes. Besides its well-established role in electron transfer reactions, NAD serves as a substrate for other biotransformations, which, at the molecular level, can be classified as protein post-translational modifications (protein deacylation, mono-, and polyADP-ribosylation) and formation of signaling molecules (e.g., cyclic ADP ribose). These biochemical reactions control many crucial biological processes, such as cellular signaling and recognition, DNA repair and epigenetic modifications, stress response, immune response, aging and senescence, and many others. However, the links between the biological effects and underlying molecular processes are often poorly understood. Moreover, NAD has recently been found to tag the 5′-ends of some cellular RNAs, but the function of these NAD-capped RNAs remains largely unrevealed. Synthetic NAD analogs are invaluable molecular tools to detect, monitor, structurally investigate, and modulate activity of NAD-related enzymes and biological processes in order to aid their deeper understanding. Here, we review the recent advances in the design and development of NAD analogs as probes for various cellular NAD-related enzymes, enzymatic inhibitors with anticancer or antimicrobial therapeutic potential, and other NAD-related chemical biology tools. We focus on research papers published within the last 10 years.
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spelling pubmed-68916372019-12-12 NAD Analogs in Aid of Chemical Biology and Medicinal Chemistry Depaix, Anais Kowalska, Joanna Molecules Review Nicotinamide adenine dinucleotide (NAD) serves as an essential redox co-factor and mediator of multiple biological processes. Besides its well-established role in electron transfer reactions, NAD serves as a substrate for other biotransformations, which, at the molecular level, can be classified as protein post-translational modifications (protein deacylation, mono-, and polyADP-ribosylation) and formation of signaling molecules (e.g., cyclic ADP ribose). These biochemical reactions control many crucial biological processes, such as cellular signaling and recognition, DNA repair and epigenetic modifications, stress response, immune response, aging and senescence, and many others. However, the links between the biological effects and underlying molecular processes are often poorly understood. Moreover, NAD has recently been found to tag the 5′-ends of some cellular RNAs, but the function of these NAD-capped RNAs remains largely unrevealed. Synthetic NAD analogs are invaluable molecular tools to detect, monitor, structurally investigate, and modulate activity of NAD-related enzymes and biological processes in order to aid their deeper understanding. Here, we review the recent advances in the design and development of NAD analogs as probes for various cellular NAD-related enzymes, enzymatic inhibitors with anticancer or antimicrobial therapeutic potential, and other NAD-related chemical biology tools. We focus on research papers published within the last 10 years. MDPI 2019-11-19 /pmc/articles/PMC6891637/ /pubmed/31752261 http://dx.doi.org/10.3390/molecules24224187 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Depaix, Anais
Kowalska, Joanna
NAD Analogs in Aid of Chemical Biology and Medicinal Chemistry
title NAD Analogs in Aid of Chemical Biology and Medicinal Chemistry
title_full NAD Analogs in Aid of Chemical Biology and Medicinal Chemistry
title_fullStr NAD Analogs in Aid of Chemical Biology and Medicinal Chemistry
title_full_unstemmed NAD Analogs in Aid of Chemical Biology and Medicinal Chemistry
title_short NAD Analogs in Aid of Chemical Biology and Medicinal Chemistry
title_sort nad analogs in aid of chemical biology and medicinal chemistry
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6891637/
https://www.ncbi.nlm.nih.gov/pubmed/31752261
http://dx.doi.org/10.3390/molecules24224187
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