Article ID Journal Published Year Pages File Type
1177672 Analytical Chemistry Research 2015 6 Pages PDF
Abstract

•A cross-platform technique for simultaneous detection and quantification of epigenetic modifications on DNA and histone proteins in one sample preparation step.•One-pot chromatin extraction from whole blood using bi-functional magnetic nanoparticles.•Development of biotin–streptavidin mediated enzyme-based immunoassay (EIA) that is highly sensitive with enhanced signal production.•The detection can be accomplished with a few nanograms of sample (usual requirement is in micro grams) that can be obtained from a drop of blood.

Chromatin contains valuable epigenetic information comprising of both DNA and post translational histone modifications. Traditionally, detection of epigenetic modifications on DNA and histone proteins requires different and elaborate preparation steps. In this study we report on a facile and unique approach for the simultaneous detection and quantification of epigenetic modifications on DNA and histone proteins in one sample preparation step. Our novel one-pot technique consists of a chromatin extraction step from whole blood using bi-functional carboxyl-functionalized magnetic nanoparticles as solid-phase absorbents. Leucocytes enrichment from blood and chromatin extracted from the leucocytes by lysis was achieved with the same carboxyl-functionalized magnetic nanoparticles. The isolated chromatin was then eluted from the magnetic nanoparticles with PBS 1×. Using the eluted chromatin as substrate, we developed a quantitative method for simultaneous detection of epigenetic modifications on DNA and histone proteins by a biotin–streptavidin mediated enzyme-based immunosorbent assay (two-step EIA) on a 96-well plate. The simultaneous detection of epigenetic modifications on DNA and histone was validated by DNA-based EIA and histone-based Western blotting analysis performed separately with conventional protocols. By coupling cell separation and chromatin purification with a simple detection module, the global epigenetic information could be evaluated in less than 8 h in leucocytes from blood. Our simplified cross-platform approach can be used by most laboratories for multiplex detection, uses non-hazardous materials and could be integrated with microfabrication methods for onchip analysis.

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Related Topics
Physical Sciences and Engineering Chemistry Analytical Chemistry
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