Umeå universitets logga

umu.sePublikationer
Ändra sökning
RefereraExporteraLänk till posten
Permanent länk

Direktlänk
Referera
Referensformat
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annat format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annat språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf
Carbamate linker strategy in solid-phase synthesis of amino-functionalized glycoconjugates for attachment to solid surfaces and investigation of protein-carbohydrate interactions
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Kemiska institutionen.
Institut für Organische Chemie, Universität Mainz, Duesbergweg 10-14, 55128 Mainz, Germany.
Otto Diels Institute of Organic Chemistry, Christiana Albertina University of Kiel,Otto-Hahn-Platz 4, 24098 Kiel, Germany.
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Kemiska institutionen.
2009 (Engelska)Ingår i: European Journal of Organic Chemistry, ISSN 1434-193X, E-ISSN 1099-0690, nr 3, s. 349-57Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Amino-functionalized serine-based galactose and glucose neoglycolipids were prepared by solid-phase synthesis using a carbamate strategy for anchoring amino functionalities to a (2-fluoro-4-hydroxymethylphenoxy)acetic acid linker resin. Key synthetic steps were monitored with gel-phase 19F NMR spectroscopy. Cleavage from the solid support was performed with trifluoroacetic acid. The terminal amine of the neoglycolipids was conjugated with didecyl squarate and then immobilized in amino-functionalized microtiter plates and the glycoconjugates were successfully probed with a galactose-binding lectin.

Ort, förlag, år, upplaga, sidor
Weinheim: WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim , 2009. nr 3, s. 349-57
Nyckelord [en]
Solid-phase synthesis, Glycoconjugates, Carbohydrates, Proteins, Carbohydrate protein interactions, Carbamate linker, Gel-phase 19F NMR spectroscopy, Microtiter plates
Nationell ämneskategori
Annan medicinsk grundvetenskap
Identifikatorer
URN: urn:nbn:se:umu:diva-11489DOI: 10.1002/ejoc.200800670Scopus ID: 2-s2.0-58649118203OAI: oai:DiVA.org:umu-11489DiVA, id: diva2:151160
Tillgänglig från: 2009-01-12 Skapad: 2009-01-12 Senast uppdaterad: 2023-03-23Bibliografiskt granskad
Ingår i avhandling
1. Glycoconjugates: synthesis and investigation of carbohydrate-protein interactions
Öppna denna publikation i ny flik eller fönster >>Glycoconjugates: synthesis and investigation of carbohydrate-protein interactions
2010 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

To study the functions of glycoconjugates in biological systems reliable and efficient protocols for glycoconjugate synthesis are needed. To reach this goal we have developed methods for solid-phase synthesis of glycoconjugates that can be monitored with gel-phase 19F spectroscopy using fluorinated linkers, building blocks, and protecting groups. We have developed a new fluorine containing linker suitable for solid-phase synthesis of glycoconjugates. The linker was more acid-labile than similar linkers in order to enable cleavage under mild conditions of the target compound from the linker resin.  A carbamate-based strategy has been applied to attach a spacer carrying an amino group to a fluorinated Wang linker for synthesis of amino-functionalized glycoconjugates using thioglycoside donors with fluorinated protective groups. Cleavage from the solid support was performed with trifluoroacetic acid and subsequent protecting group removal gave the target compound. The terminal amine was conjugated with didecyl squarate and this derivative can be attached to various proteins and solid surfaces carrying primary or secondary amines. To evaluate this methodology we have immobilized glycoconjugates in amino-functionalized microtiter plates and successfully probed them with lectin. In addition, a novel fluorine containing protecting group has been designed, synthesized and evaluated. The protecting group was used for protection of the unreactive 4-OH in a galactose building block that was applied in the synthesis of 6-aminohexyl galabioside and was removed with TBAF in THF.

Adenovirus serotype 8 (Ad8), Ad19, and Ad37 cause the severe ocular infection, epidemic keratoconjunctivities (EKC). During infection, the adenoviruses interact with sialic acid containing glycoconjugates on the epithelial cells via fiber structures extending from the viral particles. The virus particle most likely binds to the host cell in a multivalent way by simultaneously using multiple fiber proteins and binding sites. Multivalent sialic acid containing conjugates could efficiently inhibit Ad37 cell attachment and subsequent infection of human corneal epithelial (HCE) cells. Three compact tri- and tetravalent sialic acid conjugates were prepared and evaluated as inhibitors of adenoviral host cell attachment and subsequent infection and all conjugates were potent as anti-adenoviral agents. The conjugates can readily be synthesized from accessible starting materials. A crystal structure of the Ad37 fiber knob protein and the trivalent sialic acid conjugate showed that the three binding sites were all occupied by one sialic acid residue each.

Ort, förlag, år, upplaga, sidor
Umeå: Kemiska institutionen, Umeå universitet, 2010. s. 77
Nyckelord
Glycoconjugates, Carbohydrates, Galactose, Glucose, Solid-phase synthesis, SPOS, Glycosylation, Gel-phase 19F NMR spectroscopy, Fluorinated linker, Carbohydrate array, Microtiter plates, Carbohydrate-protein interactions, carbamate linker, Fsec, Protecting group, Fluorinated protecting group, Multivalent glycoconjugates, Adenovirus, Ad37, Epidemic keratoconjunctivitis, EKC, Sialic acid, Adenovirus inhibitor, Trivalent, Tetravalent, X-ray crystal structure
Nationell ämneskategori
Organisk kemi
Forskningsämne
organisk kemi
Identifikatorer
urn:nbn:se:umu:diva-33841 (URN)978-91-7459-014-2 (ISBN)
Disputation
2010-06-04, KBC-huset, KB3B1, Umeå Universitet, Umeå, 10:00 (Svenska)
Opponent
Handledare
Tillgänglig från: 2010-05-14 Skapad: 2010-05-07 Senast uppdaterad: 2018-06-08Bibliografiskt granskad

Open Access i DiVA

Fulltext saknas i DiVA

Övriga länkar

Förlagets fulltextScopus

Person

Spjut, SaraElofsson, Mikael

Sök vidare i DiVA

Av författaren/redaktören
Spjut, SaraElofsson, Mikael
Av organisationen
Kemiska institutionen
I samma tidskrift
European Journal of Organic Chemistry
Annan medicinsk grundvetenskap

Sök vidare utanför DiVA

GoogleGoogle Scholar

doi
urn-nbn

Altmetricpoäng

doi
urn-nbn
Totalt: 402 träffar
RefereraExporteraLänk till posten
Permanent länk

Direktlänk
Referera
Referensformat
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annat format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annat språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf