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Hepatocyte growth factor (HGF) in fecal samples: rapid detection by surface plasmon resonance

BACKGROUND: 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. METHOD: We utilised SPR to detect hepatocyte growth factor (HGF)...

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Autores principales: Nayeri, Fariba, Aili, Daniel, Nayeri, Tayeb, Xu, Junyang, Almer, Sven, Lundström, Ingemar, Åkerlind, Britt, Liedberg, Bo
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1090571/
https://www.ncbi.nlm.nih.gov/pubmed/15826299
http://dx.doi.org/10.1186/1471-230X-5-13
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author Nayeri, Fariba
Aili, Daniel
Nayeri, Tayeb
Xu, Junyang
Almer, Sven
Lundström, Ingemar
Åkerlind, Britt
Liedberg, Bo
author_facet Nayeri, Fariba
Aili, Daniel
Nayeri, Tayeb
Xu, Junyang
Almer, Sven
Lundström, Ingemar
Åkerlind, Britt
Liedberg, Bo
author_sort Nayeri, Fariba
collection PubMed
description BACKGROUND: 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. METHOD: We 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. RESULTS: We 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. CONCLUSION: Determination 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.
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spelling pubmed-10905712005-05-07 Hepatocyte growth factor (HGF) in fecal samples: rapid detection by surface plasmon resonance Nayeri, Fariba Aili, Daniel Nayeri, Tayeb Xu, Junyang Almer, Sven Lundström, Ingemar Åkerlind, Britt Liedberg, Bo BMC Gastroenterol Technical Advance BACKGROUND: 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. METHOD: We 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. RESULTS: We 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. CONCLUSION: Determination 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. BioMed Central 2005-04-12 /pmc/articles/PMC1090571/ /pubmed/15826299 http://dx.doi.org/10.1186/1471-230X-5-13 Text en Copyright © 2005 Nayeri et al; licensee BioMed Central Ltd.
spellingShingle Technical Advance
Nayeri, Fariba
Aili, Daniel
Nayeri, Tayeb
Xu, Junyang
Almer, Sven
Lundström, Ingemar
Åkerlind, Britt
Liedberg, Bo
Hepatocyte growth factor (HGF) in fecal samples: rapid detection by surface plasmon resonance
title Hepatocyte growth factor (HGF) in fecal samples: rapid detection by surface plasmon resonance
title_full Hepatocyte growth factor (HGF) in fecal samples: rapid detection by surface plasmon resonance
title_fullStr Hepatocyte growth factor (HGF) in fecal samples: rapid detection by surface plasmon resonance
title_full_unstemmed Hepatocyte growth factor (HGF) in fecal samples: rapid detection by surface plasmon resonance
title_short Hepatocyte growth factor (HGF) in fecal samples: rapid detection by surface plasmon resonance
title_sort hepatocyte growth factor (hgf) in fecal samples: rapid detection by surface plasmon resonance
topic Technical Advance
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1090571/
https://www.ncbi.nlm.nih.gov/pubmed/15826299
http://dx.doi.org/10.1186/1471-230X-5-13
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