Structure-activity relationships in carbohydrates revealed by their hydration
One of the more intriguing aspects of carbohydrate chemistry is that despite having very similar molecular structures, sugars have very different properties. For instance, there is a sensible difference in sweet taste between glucose and trehalose, even though trehalose is a disaccharide that compri...
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Published in | Biochimica et biophysica acta. General subjects Vol. 1861; no. 6; pp. 1486 - 1493 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
01.06.2017
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Subjects | |
Online Access | Get full text |
ISSN | 0304-4165 1872-8006 |
DOI | 10.1016/j.bbagen.2016.12.017 |
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Abstract | One of the more intriguing aspects of carbohydrate chemistry is that despite having very similar molecular structures, sugars have very different properties. For instance, there is a sensible difference in sweet taste between glucose and trehalose, even though trehalose is a disaccharide that comprised two glucose units, suggesting a different ability of these two carbohydrates to bind to sweet receptors. Here we have looked at the hydration of specific sites and at the three-dimensional configuration of water molecules around three carbohydrates (glucose, cellobiose, and trehalose), combining neutron diffraction data with computer modelling. Results indicate that identical chemical groups can have radically different hydration patterns depending on their location on a given molecule. These differences can be linked with the specific activity of glucose, cellobiose, and trehalose as a sweet substance, as building block of cellulose fiber, and as a bioprotective agent, respectively. This article is part of a Special Issue entitled “Recent Advances in Bionanomaterials” Guest Editors: Dr. Marie-Louise Saboungi and Dr. Samuel D. Bader.
•Hydration structure of carbohydrates can be used to predict biological function.•Characterization of water-carbohydrates interactions at the atomic scale.•Possible relevance for sweet taste response. |
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AbstractList | One of the more intriguing aspects of carbohydrate chemistry is that despite having very similar molecular structures, sugars have very different properties. For instance, there is a sensible difference in sweet taste between glucose and trehalose, even though trehalose is a disaccharide that comprised two glucose units, suggesting a different ability of these two carbohydrates to bind to sweet receptors. Here we have looked at the hydration of specific sites and at the three-dimensional configuration of water molecules around three carbohydrates (glucose, cellobiose, and trehalose), combining neutron diffraction data with computer modelling. Results indicate that identical chemical groups can have radically different hydration patterns depending on their location on a given molecule. These differences can be linked with the specific activity of glucose, cellobiose, and trehalose as a sweet substance, as building block of cellulose fiber, and as a bioprotective agent, respectively. This article is part of a Special Issue entitled “Recent Advances in Bionanomaterials” Guest Editors: Dr. Marie-Louise Saboungi and Dr. Samuel D. Bader. One of the more intriguing aspects of carbohydrate chemistry is that despite having very similar molecular structures, sugars have very different properties. For instance, there is a sensible difference in sweet taste between glucose and trehalose, even though trehalose is a disaccharide that comprised two glucose units, suggesting a different ability of these two carbohydrates to bind to sweet receptors. Here we have looked at the hydration of specific sites and at the three-dimensional configuration of water molecules around three carbohydrates (glucose, cellobiose, and trehalose), combining neutron diffraction data with computer modelling. Results indicate that identical chemical groups can have radically different hydration patterns depending on their location on a given molecule. These differences can be linked with the specific activity of glucose, cellobiose, and trehalose as a sweet substance, as building block of cellulose fiber, and as a bioprotective agent, respectively. This article is part of a Special Issue entitled "Recent Advances in Bionanomaterials" Guest Editors: Dr. Marie-Louise Saboungi and Dr. Samuel D. Bader.One of the more intriguing aspects of carbohydrate chemistry is that despite having very similar molecular structures, sugars have very different properties. For instance, there is a sensible difference in sweet taste between glucose and trehalose, even though trehalose is a disaccharide that comprised two glucose units, suggesting a different ability of these two carbohydrates to bind to sweet receptors. Here we have looked at the hydration of specific sites and at the three-dimensional configuration of water molecules around three carbohydrates (glucose, cellobiose, and trehalose), combining neutron diffraction data with computer modelling. Results indicate that identical chemical groups can have radically different hydration patterns depending on their location on a given molecule. These differences can be linked with the specific activity of glucose, cellobiose, and trehalose as a sweet substance, as building block of cellulose fiber, and as a bioprotective agent, respectively. This article is part of a Special Issue entitled "Recent Advances in Bionanomaterials" Guest Editors: Dr. Marie-Louise Saboungi and Dr. Samuel D. Bader. One of the more intriguing aspects of carbohydrate chemistry is that despite having very similar molecular structures, sugars have very different properties. For instance, there is a sensible difference in sweet taste between glucose and trehalose, even though trehalose is a disaccharide that comprised two glucose units, suggesting a different ability of these two carbohydrates to bind to sweet receptors. Here we have looked at the hydration of specific sites and at the three-dimensional configuration of water molecules around three carbohydrates (glucose, cellobiose, and trehalose), combining neutron diffraction data with computer modelling. Results indicate that identical chemical groups can have radically different hydration patterns depending on their location on a given molecule. These differences can be linked with the specific activity of glucose, cellobiose, and trehalose as a sweet substance, as building block of cellulose fiber, and as a bioprotective agent, respectively. This article is part of a Special Issue entitled “Recent Advances in Bionanomaterials” Guest Editors: Dr. Marie-Louise Saboungi and Dr. Samuel D. Bader. •Hydration structure of carbohydrates can be used to predict biological function.•Characterization of water-carbohydrates interactions at the atomic scale.•Possible relevance for sweet taste response. |
Author | Pardo, Luis Carlos McLain, Sylvia E. Busch, Sebastian Bruni, Fabio Ricci, Maria Antonietta Maugeri, Laura |
Author_xml | – sequence: 1 givenname: Laura surname: Maugeri fullname: Maugeri, Laura organization: Dipartimento di Scienze, Università degli Studi Roma Tre, Via della Vasca Navale 84, Roma 00146, Italy – sequence: 2 givenname: Sebastian surname: Busch fullname: Busch, Sebastian organization: German Engineering Materials Science Centre (GEMS) at Heinz Maier-Leibnitz Zentrum (MLZ), Helmholtz-Zentrum Geesthacht GmbH, Lichtenbergstr. Garching bei München 1 85747, Germany – sequence: 3 givenname: Sylvia E. surname: McLain fullname: McLain, Sylvia E. organization: Department of Biochemistry, University of Oxford, South Park Road, Oxford, Oxfordshire OX1 3QU, UK – sequence: 4 givenname: Luis Carlos surname: Pardo fullname: Pardo, Luis Carlos organization: Departament de Física i Enginyeria Nuclear, Universitat Politècnica de Catalunya Barcelona 08028, Catalonia, Spain – sequence: 5 givenname: Fabio surname: Bruni fullname: Bruni, Fabio organization: Dipartimento di Scienze, Università degli Studi Roma Tre, Via della Vasca Navale 84, Roma 00146, Italy – sequence: 6 givenname: Maria Antonietta surname: Ricci fullname: Ricci, Maria Antonietta email: mariaantonietta.ricci@uniroma3.it organization: Dipartimento di Scienze, Università degli Studi Roma Tre, Via della Vasca Navale 84, Roma 00146, Italy |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28011302$$D View this record in MEDLINE/PubMed |
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Keywords | Water Computer modelling Sweet taste Water-carbohydrates interactions Neutron diffraction Structure-function relationship |
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SubjectTerms | Carbohydrate Conformation cellobiose Cellobiose - chemistry Cellobiose - metabolism cellulosic fibers Computer modelling computers glucose Glucose - chemistry Glucose - metabolism Humans Ligands Models, Chemical Molecular Docking Simulation Neutron Diffraction receptors Receptors, G-Protein-Coupled - metabolism Signal Transduction Structure-Activity Relationship structure-activity relationships Structure-function relationship Sweet taste Taste Taste Perception trehalose Trehalose - chemistry Trehalose - metabolism Water Water - chemistry Water-carbohydrates interactions |
Title | Structure-activity relationships in carbohydrates revealed by their hydration |
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