Investigation of the interaction between peanut agglutinin and synthetic glycopolymeric multivalent ligands.
The interaction between synthetic glycoplymers bearing beta-D-galactose side groups and the lectin peanut agglutinin (PNA) was investigated by UV-difference spectroscopy and isothermal titration calorimetry (ITC). UV-difference spectroscopy indicated that the polymer-lectin interaction was stronger...
| Main Authors: | , , , |
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| Format: | Journal article |
| Language: | English |
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2005
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| _version_ | 1797075927906123776 |
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| author | Ambrosi, M Cameron, N Davis, B Stolnik, S |
| author_facet | Ambrosi, M Cameron, N Davis, B Stolnik, S |
| author_sort | Ambrosi, M |
| collection | OXFORD |
| description | The interaction between synthetic glycoplymers bearing beta-D-galactose side groups and the lectin peanut agglutinin (PNA) was investigated by UV-difference spectroscopy and isothermal titration calorimetry (ITC). UV-difference spectroscopy indicated that the polymer-lectin interaction was stronger than that between PNA and either the corresponding monomer, D-galactose or D-lactose. The thermodynamics of binding (K, DeltaG, DeltaH, DeltaS and n) were determined from ITC data by fitting with a two-site, non-cooperative binding model. It was found that the glycopolymer displayed around a 50 times greater affinity for the lectin than the parent carbohydrate, and around 10 times greater than the monomer, on a valency-corrected basis. Binding was found to be entropically driven, and was accompanied by aggregation and precipitation of protein molecules. Furthermore, interesting differences between polymers prepared either from deacetylated monomers, or by deacetylation of pre-formed polymers, were found. |
| first_indexed | 2024-03-06T23:57:08Z |
| format | Journal article |
| id | oxford-uuid:749daf40-132d-4ebd-8f9c-fd48632ccb57 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-06T23:57:08Z |
| publishDate | 2005 |
| record_format | dspace |
| spelling | oxford-uuid:749daf40-132d-4ebd-8f9c-fd48632ccb572022-03-26T20:04:07ZInvestigation of the interaction between peanut agglutinin and synthetic glycopolymeric multivalent ligands.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:749daf40-132d-4ebd-8f9c-fd48632ccb57EnglishSymplectic Elements at Oxford2005Ambrosi, MCameron, NDavis, BStolnik, SThe interaction between synthetic glycoplymers bearing beta-D-galactose side groups and the lectin peanut agglutinin (PNA) was investigated by UV-difference spectroscopy and isothermal titration calorimetry (ITC). UV-difference spectroscopy indicated that the polymer-lectin interaction was stronger than that between PNA and either the corresponding monomer, D-galactose or D-lactose. The thermodynamics of binding (K, DeltaG, DeltaH, DeltaS and n) were determined from ITC data by fitting with a two-site, non-cooperative binding model. It was found that the glycopolymer displayed around a 50 times greater affinity for the lectin than the parent carbohydrate, and around 10 times greater than the monomer, on a valency-corrected basis. Binding was found to be entropically driven, and was accompanied by aggregation and precipitation of protein molecules. Furthermore, interesting differences between polymers prepared either from deacetylated monomers, or by deacetylation of pre-formed polymers, were found. |
| spellingShingle | Ambrosi, M Cameron, N Davis, B Stolnik, S Investigation of the interaction between peanut agglutinin and synthetic glycopolymeric multivalent ligands. |
| title | Investigation of the interaction between peanut agglutinin and synthetic glycopolymeric multivalent ligands. |
| title_full | Investigation of the interaction between peanut agglutinin and synthetic glycopolymeric multivalent ligands. |
| title_fullStr | Investigation of the interaction between peanut agglutinin and synthetic glycopolymeric multivalent ligands. |
| title_full_unstemmed | Investigation of the interaction between peanut agglutinin and synthetic glycopolymeric multivalent ligands. |
| title_short | Investigation of the interaction between peanut agglutinin and synthetic glycopolymeric multivalent ligands. |
| title_sort | investigation of the interaction between peanut agglutinin and synthetic glycopolymeric multivalent ligands |
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