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Details

Autor(en) / Beteiligte
Titel
An Improved Ultrasensitive Enzyme-Linked Immunosorbent Assay Using Hydrangea-Like Antibody–Enzyme–Inorganic Three-in-One Nanocomposites
Ist Teil von
  • ACS applied materials & interfaces, 2016-03, Vol.8 (10), p.6329-6335
Ort / Verlag
United States: American Chemical Society
Erscheinungsjahr
2016
Quelle
MEDLINE
Beschreibungen/Notizen
  • Protein–inorganic nanoflowers, composed of protein and copper­(II) phosphate (Cu3(PO4)2), have recently grabbed people’s attention. Because the synthetic method requires no organic solvent and because of the distinct hierarchical nanostructure, protein–inorganic nanoflowers display enhanced catalytic activity and stability and would be a promising tool in biocatalytical processes and biological and biomedical fields. In this work, we first coimmobilized the enzyme, antibody, and Cu3(PO4)2 into a three-in-one hybrid protein–inorganic nanoflower to enable it to possess dual functions: (1) the antibody portion retains the ability to specifically capture the corresponding antigen; (2) the nanoflower has enhanced enzymatic activity and stability to produce an amplified signal. The prepared antibody–enzyme–inorganic nanoflower was first applied in an enzyme-linked immunosorbent assay to serve as a novel enzyme-labeled antibody for Escherichia coli O157:H7 (E. coli O157:H7) determination. The detection limit is 60 CFU L–1, which is far superior to commercial ELISA systems. The three-in-one antibody (anti-E. coli O157:H7 antibody)–enzyme (horseradish peroxidase)–inorganic (Cu3(PO4)2) nanoflower has some advantages over commercial enzyme–antibody conjugates. First, it is much easier to prepare and does not need any complex covalent modification. Second, it has fairly high capture capability and catalytic activity because it is presented as aggregates of abundant antibodies and enzymes. Third, it has enhanced enzymatic stability compared to the free form of enzyme due to the unique hierarchical nanostructure.
Sprache
Englisch
Identifikatoren
ISSN: 1944-8244
eISSN: 1944-8252
DOI: 10.1021/acsami.5b11834
Titel-ID: cdi_proquest_miscellaneous_1774158615

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