Document Detail


Development of fructosyl valine binding polymers by covalent imprinting.
MedLine Citation:
PMID:  17419046     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Molecularly imprinted polymers (MIPs) against fructosyl valine (Fru-Val), the N-terminal constituent of hemoglobin A1c beta-chains, were prepared by cross-linking of beta-D-Fru-Val-O-bis(4-vinylphenylboronate) with an excess of ethylene glycol dimethacrylate (EDMA) or trimethylolpropane trimethacrylate (TRIM). Control MIPs were prepared in analogy by cross-linking the corresponding vinylphenylboronate esters of fructose and pinacol. After template extraction batch rebinding studies were performed using different pH values and buffer compositions. The Fru-Val imprinted TRIM cross-linked polymer binds about 1.4 times more Fru-Val than the fructose imprinted polymer and 2.7 times more Fru-Val than pinacol imprinted polymer. The highest imprinting effect was obtained in 100 mM sodium carbonate/10% methanol (pH 11.4). The TRIM cross-linked Fru-Val imprinted polymer showed a better specificity than the EDMA cross-linked polymer. The binding of valine was very low. Thermo gravimetric analysis indicated that the generated Fru-Val imprinted polymer has high thermo stability. No change in binding was observed after incubation of the polymers in buffer at 80 degrees C for 36 h. Since the functional group of the polymers (phenyl boronic acid) targets the sugar part of Fru-Val the imprint technique used should also be applicable for the development of MIPs against other glycated amino acids and peptides.
Authors:
Rajagopal Rajkumar; Axel Warsinke; Helmuth Möhwald; Frieder W Scheller; Martin Katterle
Related Documents :
15777166 - Four-year follow-up of poly-l-lactic acid cages for lumbar interbody fusion in goats.
17336066 - Synthesis and characterisation of a new ph-sensitive amphotericin b--poly(ethylene glyc...
1064016 - Elucidation of hydrocarbon structure in an enzyme-catalyzed benzo[a]pyrene-poly (g) cov...
19093646 - Enamel deproteinization and its effect on acid etching: an in vitro study.
6867606 - Why concentration of serum ferritin does not in all circumstances reflect storage iron ...
14732686 - Direct interactions between epstein-barr virus leader protein lp and the ebna2 acidic d...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2007-03-07
Journal Detail:
Title:  Biosensors & bioelectronics     Volume:  22     ISSN:  0956-5663     ISO Abbreviation:  Biosens Bioelectron     Publication Date:  2007 Jun 
Date Detail:
Created Date:  2007-05-21     Completed Date:  2007-07-26     Revised Date:  2009-07-14    
Medline Journal Info:
Nlm Unique ID:  9001289     Medline TA:  Biosens Bioelectron     Country:  England    
Other Details:
Languages:  eng     Pagination:  3318-25     Citation Subset:  IM    
Affiliation:
Analytical Biochemistry, Potsdam University, D-14476 Potsdam, Germany.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Hemoglobin A, Glycosylated / analysis*
Humans
Hydroxylamines
Methacrylates / chemistry*
Polymers / chemistry*
Temperature
Valine / analogs & derivatives*,  chemistry
Chemical
Reg. No./Substance:
0/Hemoglobin A, Glycosylated; 0/Hydroxylamines; 0/Methacrylates; 0/N,O-dimethacryloylhydroxylamine; 0/Polymers; 0/hemoglobin A1c protein, human; 10003-64-2/fructosylvaline; 3290-92-4/trimethylolpropane trimethacrylate; 7004-03-7/Valine; 97-90-5/ethylene dimethacrylate

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Life cycle assessment of a national policy proposal - the case of a Swedish waste incineration tax.
Next Document:  Structural aspects of AMPA receptor activation, desensitization and deactivation.