Abstract

BackgroundThe development of biosensors, based on surface plasmon resonance (SPR) technology, enables monitoring of a variety of biospecific interactions without the need for chemical-, biological- or radiological-labelled reagents.MethodWe utilised SPR to detect hepatocyte growth factor (HGF) in reconstituted faecal samples and studied samples from patients with infectious gastroenteritis (n = 20) and normal controls (n = 10). Mouse anti-human HGF monoclonal antibodies and recombinant human HGF receptor (c-Met)/Fc chimera were immobilised in flow cells of a CM5 biosensor chip.ResultsWe found that infectious gastroenteritis produced a higher signal response compared to controls, due to binding of HGF to monoclonal anti-HGF antibody as well as binding of HGF to c-Met receptor (p < 0.01). The SPR signal response correlated with results from ELISA (r = 72%, p > 0.001). The signal response decreased significantly (p < 0.05) when samples were diluted with dextran, because of reduction in both specific as well as unspecific binding of HGF to dextran. The decrease in the specific response might imply that the dextran- binding site for HGF overlaps with the antibody binding epitope, or that dextran binding induces a conformational change of the HGF molecule. Bands corresponding to HGF were found by gel electrophoresis of purified faeces in an affinity chromatography column immobilised by HGF ligands.ConclusionDetermination of HGF by SPR might be beneficial in diagnosis of acute situations that present with symptoms of gastroenteritis and may, possibly, guide appropriate medical treatments. This is to our knowledge the first report on the use of SPR for detection of HGF in faeces samples.

Highlights

  • The development of biosensors, based on surface plasmon resonance (SPR) technology, enables monitoring of a variety of biospecific interactions without the need for chemical, biological- or radiological-labelled reagents

  • Correlation with ELISA Determination of hepatocyte growth factor (HGF) in faeces by utilising SPR correlated significantly (n = 20, r = 72%, p < 0.001) with the levels measured by ELISA (Fig 3)

  • Correlation with age We found a negative correlation between the SPR signal intensity and age in patients with infectious gastroenteritis (n = 20, r = - 0.55, p = 0.010) (Fig 4)

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Summary

Introduction

The development of biosensors, based on surface plasmon resonance (SPR) technology, enables monitoring of a variety of biospecific interactions without the need for chemical-, biological- or radiological-labelled reagents. The change in refractive index will shift the angle of incidence at which the SPR excitation occurs. This shift in the angle is tracked by monitoring the movement of intensity minima of the reflected light with time using the Kretschmann configuration, and the binding event is presented as a sensorgram [1]. The sensor surface of the SPR apparatus consists of a carboxy-methylated dextran matrix, which is a hydrogel providing a solution-like environment in which the biospecific interactions occur. The carboxyl groups in the dextran matrix enable covalent coupling of ligands (proteins, receptors, DNA etc) to the surface

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