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Unveiling the Shape of N-Acetylgalactosamine: A Cancer-Associated Sugar Derivative

[Image: see text] In the present work, we report the first rotational study of N-acetylgalactosamine, a cancer-associated sugar derivative, by means of high-resolution rotational spectroscopy. Two different conformers have been conclusively characterized using broadband Fourier transform microwave s...

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Autores principales: Aguado, R., Sanz-Novo, M., Mata, S., León, I., Alonso, J. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9620139/
https://www.ncbi.nlm.nih.gov/pubmed/36099577
http://dx.doi.org/10.1021/acs.jpca.2c04595
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author Aguado, R.
Sanz-Novo, M.
Mata, S.
León, I.
Alonso, J. L.
author_facet Aguado, R.
Sanz-Novo, M.
Mata, S.
León, I.
Alonso, J. L.
author_sort Aguado, R.
collection PubMed
description [Image: see text] In the present work, we report the first rotational study of N-acetylgalactosamine, a cancer-associated sugar derivative, by means of high-resolution rotational spectroscopy. Two different conformers have been conclusively characterized using broadband Fourier transform microwave spectroscopy coupled with a laser ablation vaporization system. Additionally, we performed a comprehensive analysis of the intramolecular interactions that govern these structures, which allowed us to both characterize the existence of intramolecular hydrogen bond networks that drive the intrinsic conformation panorama of N-acetylgalactosamine and further rationalize the biological role of this aminosugar derivative as part of the Tn antigen.
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spelling pubmed-96201392022-11-01 Unveiling the Shape of N-Acetylgalactosamine: A Cancer-Associated Sugar Derivative Aguado, R. Sanz-Novo, M. Mata, S. León, I. Alonso, J. L. J Phys Chem A [Image: see text] In the present work, we report the first rotational study of N-acetylgalactosamine, a cancer-associated sugar derivative, by means of high-resolution rotational spectroscopy. Two different conformers have been conclusively characterized using broadband Fourier transform microwave spectroscopy coupled with a laser ablation vaporization system. Additionally, we performed a comprehensive analysis of the intramolecular interactions that govern these structures, which allowed us to both characterize the existence of intramolecular hydrogen bond networks that drive the intrinsic conformation panorama of N-acetylgalactosamine and further rationalize the biological role of this aminosugar derivative as part of the Tn antigen. American Chemical Society 2022-09-13 2022-10-27 /pmc/articles/PMC9620139/ /pubmed/36099577 http://dx.doi.org/10.1021/acs.jpca.2c04595 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Aguado, R.
Sanz-Novo, M.
Mata, S.
León, I.
Alonso, J. L.
Unveiling the Shape of N-Acetylgalactosamine: A Cancer-Associated Sugar Derivative
title Unveiling the Shape of N-Acetylgalactosamine: A Cancer-Associated Sugar Derivative
title_full Unveiling the Shape of N-Acetylgalactosamine: A Cancer-Associated Sugar Derivative
title_fullStr Unveiling the Shape of N-Acetylgalactosamine: A Cancer-Associated Sugar Derivative
title_full_unstemmed Unveiling the Shape of N-Acetylgalactosamine: A Cancer-Associated Sugar Derivative
title_short Unveiling the Shape of N-Acetylgalactosamine: A Cancer-Associated Sugar Derivative
title_sort unveiling the shape of n-acetylgalactosamine: a cancer-associated sugar derivative
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9620139/
https://www.ncbi.nlm.nih.gov/pubmed/36099577
http://dx.doi.org/10.1021/acs.jpca.2c04595
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