Antigenic properties of the GroEL-like protein of Campylobacter rectus

The purpose of this study was to clarify the antigenic properties of the GroEL‐like protein of Campylobacter rectus using a specific polyclonal antibody directed to the purified 64‐kDa GroEL‐like protein (pAb‐CrGroEL), a polyclonal antibody directed to the Actinobacillus actinomycetemcomitans GroEL‐...

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Veröffentlicht in:Oral microbiology and immunology 2002-02, Vol.17 (1), p.16-21
Hauptverfasser: Hinode, D., Yokoyama, M., Tanabe, S., Yoshioka, M., Nakamura, R.
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Yokoyama, M.
Tanabe, S.
Yoshioka, M.
Nakamura, R.
description The purpose of this study was to clarify the antigenic properties of the GroEL‐like protein of Campylobacter rectus using a specific polyclonal antibody directed to the purified 64‐kDa GroEL‐like protein (pAb‐CrGroEL), a polyclonal antibody directed to the Actinobacillus actinomycetemcomitans GroEL‐like protein (pAb‐AaGroEL) and a monoclonal antibody against the recombinant human HSP60 (mAb‐HuHSP60). In SDS‐PAGE/Western immunoblotting analysis, mAb‐HuHSP60, pAb‐CrGroEL and pAb‐AaGroEL were found to react with the GroEL‐like protein (64‐kDa) present in all C. rectus strains. A 150‐kDa protein in C. rectus ATCC 33238 also reacted strongly with pAb‐CrGroEL. This 150‐kDa protein was found to be present on the surface‐associated material of bacterial cells, as determined by transmission electron microscopy and immunogold labelling of cells with pAb‐CrGroEL. Analysis of the first 20 N‐terminal amino acids of the sequence of the 150‐kDa protein revealed a strong homology (80%) with the C. rectus surface layer (S‐layer) protein. Investigation of the biochemical nature of antigenic determinants using periodic acid and proteolytic enzymes showed that the C. rectus GroEL‐like protein possessed immunodominant epitopes in both peptide and carbohydrate chains, and that the immunoreactive determinants of the 150‐kDa protein belonged to carbohydrate. These results suggest that the GroEL‐like protein and the S‐layer protein of C. rectus may share the same carbohydrate epitopes.
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In SDS‐PAGE/Western immunoblotting analysis, mAb‐HuHSP60, pAb‐CrGroEL and pAb‐AaGroEL were found to react with the GroEL‐like protein (64‐kDa) present in all C. rectus strains. A 150‐kDa protein in C. rectus ATCC 33238 also reacted strongly with pAb‐CrGroEL. This 150‐kDa protein was found to be present on the surface‐associated material of bacterial cells, as determined by transmission electron microscopy and immunogold labelling of cells with pAb‐CrGroEL. Analysis of the first 20 N‐terminal amino acids of the sequence of the 150‐kDa protein revealed a strong homology (80%) with the C. rectus surface layer (S‐layer) protein. Investigation of the biochemical nature of antigenic determinants using periodic acid and proteolytic enzymes showed that the C. rectus GroEL‐like protein possessed immunodominant epitopes in both peptide and carbohydrate chains, and that the immunoreactive determinants of the 150‐kDa protein belonged to carbohydrate. 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In SDS‐PAGE/Western immunoblotting analysis, mAb‐HuHSP60, pAb‐CrGroEL and pAb‐AaGroEL were found to react with the GroEL‐like protein (64‐kDa) present in all C. rectus strains. A 150‐kDa protein in C. rectus ATCC 33238 also reacted strongly with pAb‐CrGroEL. This 150‐kDa protein was found to be present on the surface‐associated material of bacterial cells, as determined by transmission electron microscopy and immunogold labelling of cells with pAb‐CrGroEL. Analysis of the first 20 N‐terminal amino acids of the sequence of the 150‐kDa protein revealed a strong homology (80%) with the C. rectus surface layer (S‐layer) protein. Investigation of the biochemical nature of antigenic determinants using periodic acid and proteolytic enzymes showed that the C. rectus GroEL‐like protein possessed immunodominant epitopes in both peptide and carbohydrate chains, and that the immunoreactive determinants of the 150‐kDa protein belonged to carbohydrate. These results suggest that the GroEL‐like protein and the S‐layer protein of C. rectus may share the same carbohydrate epitopes.</description><subject>Actinobacillus actinomycetemcomitans</subject><subject>Aggregatibacter actinomycetemcomitans - immunology</subject><subject>antigenic property</subject><subject>Antigens, Bacterial</subject><subject>Bacterial Outer Membrane Proteins - immunology</subject><subject>Bacterial Proteins</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Campylobacter - immunology</subject><subject>Campylobacter rectus</subject><subject>Chaperonin 60 - immunology</subject><subject>Dentistry</subject><subject>Epitopes</subject><subject>Fundamental and applied biological sciences. 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Psychology</topic><topic>GroEL-like protein</topic><topic>Humans</topic><topic>Membrane Glycoproteins</topic><topic>Microbiology</topic><topic>Morphology, structure, chemical composition</topic><topic>S-layer protein</topic><topic>Sequence Homology, Amino Acid</topic><toplevel>online_resources</toplevel><creatorcontrib>Hinode, D.</creatorcontrib><creatorcontrib>Yokoyama, M.</creatorcontrib><creatorcontrib>Tanabe, S.</creatorcontrib><creatorcontrib>Yoshioka, M.</creatorcontrib><creatorcontrib>Nakamura, R.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Oral microbiology and immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hinode, D.</au><au>Yokoyama, M.</au><au>Tanabe, S.</au><au>Yoshioka, M.</au><au>Nakamura, R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antigenic properties of the GroEL-like protein of Campylobacter rectus</atitle><jtitle>Oral microbiology and immunology</jtitle><addtitle>Oral Microbiol Immunol</addtitle><date>2002-02</date><risdate>2002</risdate><volume>17</volume><issue>1</issue><spage>16</spage><epage>21</epage><pages>16-21</pages><issn>0902-0055</issn><eissn>1399-302X</eissn><coden>OMIMEE</coden><abstract>The purpose of this study was to clarify the antigenic properties of the GroEL‐like protein of Campylobacter rectus using a specific polyclonal antibody directed to the purified 64‐kDa GroEL‐like protein (pAb‐CrGroEL), a polyclonal antibody directed to the Actinobacillus actinomycetemcomitans GroEL‐like protein (pAb‐AaGroEL) and a monoclonal antibody against the recombinant human HSP60 (mAb‐HuHSP60). In SDS‐PAGE/Western immunoblotting analysis, mAb‐HuHSP60, pAb‐CrGroEL and pAb‐AaGroEL were found to react with the GroEL‐like protein (64‐kDa) present in all C. rectus strains. A 150‐kDa protein in C. rectus ATCC 33238 also reacted strongly with pAb‐CrGroEL. This 150‐kDa protein was found to be present on the surface‐associated material of bacterial cells, as determined by transmission electron microscopy and immunogold labelling of cells with pAb‐CrGroEL. Analysis of the first 20 N‐terminal amino acids of the sequence of the 150‐kDa protein revealed a strong homology (80%) with the C. rectus surface layer (S‐layer) protein. Investigation of the biochemical nature of antigenic determinants using periodic acid and proteolytic enzymes showed that the C. rectus GroEL‐like protein possessed immunodominant epitopes in both peptide and carbohydrate chains, and that the immunoreactive determinants of the 150‐kDa protein belonged to carbohydrate. These results suggest that the GroEL‐like protein and the S‐layer protein of C. rectus may share the same carbohydrate epitopes.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science, Ltd</pub><pmid>11860551</pmid><doi>10.1046/j.0902-0055.2001.00086.x</doi><tpages>6</tpages></addata></record>
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subjects Actinobacillus actinomycetemcomitans
Aggregatibacter actinomycetemcomitans - immunology
antigenic property
Antigens, Bacterial
Bacterial Outer Membrane Proteins - immunology
Bacterial Proteins
Bacteriology
Biological and medical sciences
Blotting, Western
Campylobacter - immunology
Campylobacter rectus
Chaperonin 60 - immunology
Dentistry
Epitopes
Fundamental and applied biological sciences. Psychology
GroEL-like protein
Humans
Membrane Glycoproteins
Microbiology
Morphology, structure, chemical composition
S-layer protein
Sequence Homology, Amino Acid
title Antigenic properties of the GroEL-like protein of Campylobacter rectus
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