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J R Soc Interface ; 11(99)2014 Oct 06.
Article in English | MEDLINE | ID: mdl-25100324

ABSTRACT

In this paper, we report on a general approach for the detection of a specific tumoural biomarker directly in serum. Such detection is made possible using a protein-binding peptide selected through an improved phage display technique and then conjugated to engineered microparticles (MPs). Protein biomarkers represent an unlimited source of information for non-invasive diagnostic and prognostic tests; MP-based assays are becoming largely used in manipulation of soluble biomarkers, but their direct use in serum is hampered by the complex biomolecular environment. Our technique overcomes the current limitations as it produces a selective MP--engineered with an antifouling layer--that 'captures' the relevant protein staying impervious to the background. Our system succeeds in fishing-out the human tumour necrosis factor alpha directly in serum with a high selectivity degree. Our method could have great impact in soluble protein manipulation and detection for a wide variety of diagnostic applications.


Subject(s)
Biomarkers, Tumor/blood , Blood Proteins/isolation & purification , Peptides/metabolism , Blood Proteins/metabolism , Calorimetry , Cell Surface Display Techniques , Chromatography, High Pressure Liquid , Enzyme-Linked Immunosorbent Assay , Fluorescence , Humans , Microfluidic Analytical Techniques , Microscopy, Confocal , Microscopy, Electron, Transmission , Protein Binding , Solubility , Tumor Necrosis Factor-alpha/blood , Tumor Necrosis Factor-alpha/isolation & purification
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