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Lactose and Galactose Promote the Crystallization of Human Galectin-10

Galectin-10 (Gal-10) forms Charcot–Leyden crystals (CLCs), which play a key role in the symptoms of asthma and allergies and some other diseases. Gal-10 has a carbohydrate-binding site; however, neither the Gal-10 dimer nor the CLCs can bind sugars. To investigate the monomer–dimer equilibrium of Ga...

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Autores principales: Fu, Yu-Fan, Jiang, Si-Cong, Zhang, Zhong-Wei, Yang, Xin-Yue, Li, Zi-Lin, Hu, Jing, Yuan, Shu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9966682/
https://www.ncbi.nlm.nih.gov/pubmed/36838965
http://dx.doi.org/10.3390/molecules28041979
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author Fu, Yu-Fan
Jiang, Si-Cong
Zhang, Zhong-Wei
Yang, Xin-Yue
Li, Zi-Lin
Hu, Jing
Yuan, Shu
author_facet Fu, Yu-Fan
Jiang, Si-Cong
Zhang, Zhong-Wei
Yang, Xin-Yue
Li, Zi-Lin
Hu, Jing
Yuan, Shu
author_sort Fu, Yu-Fan
collection PubMed
description Galectin-10 (Gal-10) forms Charcot–Leyden crystals (CLCs), which play a key role in the symptoms of asthma and allergies and some other diseases. Gal-10 has a carbohydrate-binding site; however, neither the Gal-10 dimer nor the CLCs can bind sugars. To investigate the monomer–dimer equilibrium of Gal-10, high-performance size-exclusion chromatography (SEC) was employed to separate serial dilutions of Gal-10 with and without carbohydrates. We found that both the dimerization and crystallization of Gal-10 were promoted by lactose/galactose binding. A peak position shift for the monomer was observed after treatment with either lactose or galactose, implying that the polarity of the monomer was reduced by lactose/galactose binding. Further experiments indicated that alkaline conditions of pH 8.8 mimicked the lactose/galactose-binding environment, and the time interval between monomers and dimers in the chromatogram decreased from 0.8 min to 0.4 min. Subsequently, the electrostatic potential of the Gal-10 monomers was computed. After lactose/galactose binding, the top side of the monomer shifted from negatively charged to electrically neutral, allowing it to interact with the carbohydrate-binding site of the opposing subunit during dimerization. Since lactose/galactose promotes the crystallization of Gal-10, our findings implied that dairy-free diets (free of lactose/galactose) might be beneficial to patients with CLC-related diseases.
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spelling pubmed-99666822023-02-26 Lactose and Galactose Promote the Crystallization of Human Galectin-10 Fu, Yu-Fan Jiang, Si-Cong Zhang, Zhong-Wei Yang, Xin-Yue Li, Zi-Lin Hu, Jing Yuan, Shu Molecules Article Galectin-10 (Gal-10) forms Charcot–Leyden crystals (CLCs), which play a key role in the symptoms of asthma and allergies and some other diseases. Gal-10 has a carbohydrate-binding site; however, neither the Gal-10 dimer nor the CLCs can bind sugars. To investigate the monomer–dimer equilibrium of Gal-10, high-performance size-exclusion chromatography (SEC) was employed to separate serial dilutions of Gal-10 with and without carbohydrates. We found that both the dimerization and crystallization of Gal-10 were promoted by lactose/galactose binding. A peak position shift for the monomer was observed after treatment with either lactose or galactose, implying that the polarity of the monomer was reduced by lactose/galactose binding. Further experiments indicated that alkaline conditions of pH 8.8 mimicked the lactose/galactose-binding environment, and the time interval between monomers and dimers in the chromatogram decreased from 0.8 min to 0.4 min. Subsequently, the electrostatic potential of the Gal-10 monomers was computed. After lactose/galactose binding, the top side of the monomer shifted from negatively charged to electrically neutral, allowing it to interact with the carbohydrate-binding site of the opposing subunit during dimerization. Since lactose/galactose promotes the crystallization of Gal-10, our findings implied that dairy-free diets (free of lactose/galactose) might be beneficial to patients with CLC-related diseases. MDPI 2023-02-19 /pmc/articles/PMC9966682/ /pubmed/36838965 http://dx.doi.org/10.3390/molecules28041979 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Fu, Yu-Fan
Jiang, Si-Cong
Zhang, Zhong-Wei
Yang, Xin-Yue
Li, Zi-Lin
Hu, Jing
Yuan, Shu
Lactose and Galactose Promote the Crystallization of Human Galectin-10
title Lactose and Galactose Promote the Crystallization of Human Galectin-10
title_full Lactose and Galactose Promote the Crystallization of Human Galectin-10
title_fullStr Lactose and Galactose Promote the Crystallization of Human Galectin-10
title_full_unstemmed Lactose and Galactose Promote the Crystallization of Human Galectin-10
title_short Lactose and Galactose Promote the Crystallization of Human Galectin-10
title_sort lactose and galactose promote the crystallization of human galectin-10
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9966682/
https://www.ncbi.nlm.nih.gov/pubmed/36838965
http://dx.doi.org/10.3390/molecules28041979
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