about
P184
Mechanistic Investigations into the Application of Sulfoxides in Carbohydrate SynthesisThermodynamics of binding of 2-methoxy-3-isopropylpyrazine and 2-methoxy-3-isobutylpyrazine to the major urinary proteinLarge oligosaccharide-based glycodendrimers.Chemically defined sialoside scaffolds for investigation of multivalent interactions with sialic acid binding proteins.Design and synthesis of glycodendrimers.Discovery of novel FabF ligands inspired by platensimycin by integrating structure-based design with diversity-oriented synthetic accessibility.Multivalent glycoconjugates as anti-pathogenic agentsTemplating carbohydrate-functionalised polymer-scaffolded dynamic combinatorial libraries with lectins.Methylthioxylose--a jewel in the mycobacterial crown?Bacterial toxin inhibitors based on multivalent scaffolds.Tetra- versus Pentavalent Inhibitors of Cholera Toxin.Dissecting Multivalent Lectin-Carbohydrate Recognition Using Polyvalent Multifunctional Glycan-Quantum Dots.Molecular Recognition-Mediated Transformation of Single-Chain Polymer Nanoparticles into Crosslinked Polymer Films.Compact, Polyvalent Mannose Quantum Dots as Sensitive, Ratiometric FRET Probes for Multivalent Protein-Ligand Interactions.Benzyne arylation of oxathiane glycosyl donors.Design, synthesis and in vitro evaluation of novel bivalent S-adenosylmethionine analogues.Compact, Polyvalent Mannose Quantum Dots as Sensitive, Ratiometric FRET Probes for Multivalent Protein-Ligand Interactions.A protein-based pentavalent inhibitor of the cholera toxin B-subunit.Spirillum Fever in IndiaTowards a structural basis for the relationship between blood group and the severity of El Tor cholera.Mechanistic studies on a sulfoxide transfer reaction mediated by diphenyl sulfoxide/triflic anhydride.Neighbouring group participation vs. addition to oxacarbenium ions: studies on the synthesis of mycobacterial oligosaccharides.Stereoselective glycosylation using oxathiane glycosyl donors.Large-scale millisecond intersubunit dynamics in the B subunit homopentamer of the toxin derived from Escherichia coli O157.Dissecting the cholera toxin-ganglioside GM1 interaction by isothermal titration calorimetry.Identification of the 5-methylthiopentosyl substituent in Mycobacterium tuberculosis lipoarabinomannan.Do glycosyl sulfonium ions engage in neighbouring-group participation? A study of oxathiane glycosyl donors and the basis for their stereoselectivity.Multivalency and cooperativity in supramolecular chemistry.A natural carbohydrate substrate for Mycobacterium tuberculosis methionine sulfoxide reductase A.Probing Multivalent Protein-Carbohydrate Interactions by Quantum Dot-Förster Resonance Energy Transfer.On the value of c: can low affinity systems be studied by isothermal titration calorimetry?Confirmation of a Protein-Protein Interaction in the Pantothenate Biosynthetic Pathway by Using Sortase-Mediated Labelling.Depsipeptide substrates for sortase-mediated N-terminal protein ligation.Carbohydrate inhibitors of cholera toxin.Efficient N-terminal labeling of proteins by use of sortase.Stereoselective glycosylations using oxathiane spiroketal glycosyl donors.Conformer-independent ureidoimidazole motifs--tools to probe conformational and tautomeric effects on the molecular recognition of triply hydrogen-bonded heterodimers.Studies on the synthesis of Lewis-y oligosaccharides.The influence of ligand valency on aggregation mechanisms for inhibiting bacterial toxins.A Protein-Based Pentavalent Inhibitor of the Cholera Toxin B-Subunit
P50
3D Volume Microscopy and TEM Sample Preparation of Complex Hybrid Nanostructures14-ERASynBio: Synthetic Glycobiology - new strategies to build and functionalise proto-cells and proto-tissuesProbing biomolecular interactions by combining ETD-tandem mass spectrometry with chemical footprinting methodologies
P710
Q26770205-385EA359-5C9E-4283-9430-CA2AB1A96CECQ27643110-20C58DE5-5BC9-4D75-B059-EFE5391AB6ABQ31121771-99FBF45B-00BD-4DA8-95FE-8C3BFC24AE48Q33194180-5ECC61CD-1629-47BA-8AF3-C8A8E75978FFQ34692328-D6B0E9B1-CEAC-4A12-997C-1C6231B23039Q35052785-72AEFABE-152E-4F10-AF1D-4B10CAA742A0Q35444698-E264A2AA-CC7C-46A2-9BA2-0C3BDF503D92Q35544423-A9027F70-F33F-4AA2-9E24-2342B3799A37Q38009185-1366F542-B84C-47BA-8B53-221479D216E8Q38069445-E9F792FB-9BF3-49A9-B5D2-523DC7D144D0Q38295903-3825CF69-8A1B-488C-8A2B-8EFAC095BF7CQ40044194-C1836FAA-04E6-46C0-B6A1-52FF12749771Q40083983-7b45824a-4239-8868-a830-b0580888c7afQ40091292-D5574C22-3675-4921-A2E1-4A09496FE267Q40587864-50E03ADB-59A9-4AB8-A042-020AC22AE41FQ40686626-FC434BDA-6323-473B-B41B-CAD0F68BCB62Q40750350-641F6D2F-D1B3-4087-9C2D-7D85C6BC706BQ41125286-02B510C5-D07E-4706-878B-8A9FB52A96BFQ41924257-7180B993-CE56-49F7-B7A5-14229EEA429BQ42027535-CF7CE1CD-3A15-4DDA-BD9D-79F589087808Q42143453-C24C8D5B-F22F-46AB-8E3E-5D54BC960EFAQ43243919-E30AF3CA-A839-42C2-B859-0831240E6E58Q43269969-D3D106B9-7DBB-47A3-85BD-06312B74F983Q44626334-45231BD4-D265-4533-B6EC-9E18DE58838AQ44744391-D809A54E-0A76-4B3C-AC5D-153C1028EF4AQ44993198-7FFD79C7-2751-486A-9190-83FF76E59648Q45835674-401E20DB-530D-43C9-8F6F-0563D7A36FE3Q46077024-3E94259B-02F4-4925-8248-53DBD616DB23Q46198806-B785226B-ADA0-4457-8C8B-D4529D617C47Q47227480-AF7720F0-19EB-45D9-B60A-9A7EA56888C2Q47357121-76C6BD3C-1AF6-4EF2-BCB1-6F5167B8C962Q48252468-ECBE48AF-B356-4E95-A61E-B87B6A33BA93Q51759823-966ADAA1-61E6-4576-9357-55A06EFF2195Q52803001-740887A5-1106-4BF9-8D1A-B63044A478C1Q52842782-D50EF2A8-DC9D-4F61-855F-B4F413C16EC8Q52844377-41BFD555-19F2-478B-933C-B6B81CFD2CA6Q52844578-D3DDA699-4052-41FF-B83F-B4411E537B8AQ52845155-010B2306-84BB-417D-92D5-A758966C0393Q52850490-20F4B7B6-16AF-4382-B7CD-CF039AABA8C2Q56512913-C3FE9805-D420-4069-B356-F03A093A4856
P50
description
researcher
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Bruce Turnbull
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Bruce Turnbull
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Bruce Turnbull
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Bruce Turnbull
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wbturnbull