4.8 Article

Benzoboroxole-Functionalized Magnetic Core/Shell Microspheres for Highly Specifi c Enrichment of Glycoproteins under Physiological Conditions

Journal

SMALL
Volume 10, Issue 7, Pages 1379-1386

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.201302841

Keywords

Fe3O4; PAA-AOPB core; shell microspheres; benzoboroxole; selective enrichment; glycoproteins; physiological condition

Funding

  1. National Science and Technology Key Project of China [2012AA020204]
  2. National Science Foundation of China [21034003, 21128001, 51073040]
  3. Science and Technology Commission of Shanghai [13JC1400500, 13520720200]

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Efficient enrichment of specific glycoproteins from complex biological samples is of great importance towards the discovery of disease biomarkers in biological systems. Recently, phenylboronic acid-based functional materials have been widely used for enrichment of glycoproteins. However, such enrichment was mainly carried out under alkaline conditions, which is different to the status of glycoproteins in neutral physiological conditions and may cause some unpredictable degradation. In this study, on-demand neutral enrichment of glycoproteins from crude biological samples is accomplished by utilizing the reversible interaction between the cis-diols of glycoproteins and benzoboroxole-functionalized magnetic composite microspheres (Fe3O4/PAA-AOPB). The Fe3O4/PAA-AOPB composite microspheres are deliberately designed and constructed with a high-magnetic-response magnetic supraparticle (MSP) core and a crosslinked poly(acrylic acid) (PAA) shell anchoring abundant benzoboroxole functional groups on the surface. These nanocomposites possessed many merits, such as large enrichment capacity (93.9 mg/g, protein/beads), low non-specific adsorption, quick enrichment process (10 min) and magnetic separation speed (20 s), and high recovery efficiency. Furthermore, the as-prepared Fe3O4/PAA-AOPB microspheres display high selectivity to glycoproteins even in the E. coli lysate or fetal bovine serum, showing great potential in the identify of low-abundance glycoproteins as biomarkers in real complex biological systems for clinical diagnoses.

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