Voltammetric determination of Os(VI)-modified oligosaccharides at nanomolar level
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
22763419
DOI
10.1016/j.bioelechem.2012.04.005
PII: S1567-5394(12)00076-X
Knihovny.cz E-resources
- MeSH
- Adsorption MeSH
- Alkenes chemistry MeSH
- Time Factors MeSH
- Electrochemistry instrumentation methods MeSH
- Electrodes MeSH
- Limit of Detection MeSH
- Oligosaccharides analysis chemistry MeSH
- Organometallic Compounds chemistry MeSH
- Osmium chemistry MeSH
- Mercury chemistry MeSH
- Temperature MeSH
- Carbon chemistry MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- 2,3-dimethyl-2-butene MeSH Browser
- Alkenes MeSH
- mannopentaose MeSH Browser
- Oligosaccharides MeSH
- Organometallic Compounds MeSH
- Osmium MeSH
- Mercury MeSH
- Carbon MeSH
Glycoproteins participate in various biological events, including disease progression. Currently, there is a pressing need for development of new simple and inexpensive methods for glycoprotein carbohydrate component (mostly oligosaccharides, OLSs) analysis and electrochemical methods were little applied in their analysis. Polysaccharides and OLS were long time considered as electroinactive compounds. We show that OLS adducts with six-valent osmium complexes are electroactive and can be determined at mercury and carbon electrodes. Adducts of OLSs with complex of Os(VI) with N,N,N',N'-tetramethylethylenediamine (tmen) can be prepared by mixing of OLS with [Os(VI)tmen] either at 37°C overnight or at 75°C in 10-15min. We modified 3α,6α-mannopentaose (MPO), stachyose and γ-cyclodextrin with [Os(VI)tmen]. The OLS adducts produced CV redox couples at hanging mercury drop electrode (HMDE) and at pyrolytic graphite electrode (PGE). 6nM MPO was determined by conventional adsorptive stripping at HMDE with RSD 5.3% directly in the reaction mixture. Similar determination at PGE was much less sensitive. Using adsorptive transfer (ex situ) stripping at PGE, μL volumes of OLS were sufficient for the analysis. Protein glycosylation stands at present in focus of medicinal chemistry because of its importance in various diseases and their diagnostics. Our paper represents first steps toward application of electrochemical methods in biomedical analysis of OLS.
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