Isolation of dermatan sulfate proteoglycans from mature bovine articular cartilages
Two species of dermatan sulfate proteoglycans, called DS-PGI and DS-PGII, have been isolated from mature bovine articular cartilages. On sodium dodecyl sulfate-polyacrylamide gel electrophoresis at low ionic strength in 0.01 M phosphate the dermatan sulfate proteoglycans appeared as a single polydis...
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Veröffentlicht in: | The Journal of biological chemistry 1985-05, Vol.260 (10), p.6304-6313 |
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description | Two species of dermatan sulfate proteoglycans, called DS-PGI and DS-PGII, have been isolated from mature bovine articular cartilages. On sodium dodecyl sulfate-polyacrylamide gel electrophoresis at low ionic strength in 0.01 M phosphate the dermatan sulfate proteoglycans appeared as a single polydisperse species whose molecular weight ranged from 80,000 to 140,000. The dermatan sulfate proteoglycans eluted as a single peak on Sepharose CL-4B chromatography in 4 M guanidine hydrochloride and showed no tendency to separate into two components. Following chondroitinase AC and ABC digestion, a core protein was obtained whose molecular weight was 45,000. However, what appeared to be a single dermatan sulfate proteoglycan was consistently separated into two species of distinctly different mobilities by sodium dodecyl sulfate-polyacrylamide gel electrophoresis at high ionic strength in 0.375 M Tris. The molecular weight of the smaller species (DS-PGII) ranged from 87,000 to 120,000. The molecular weight of the larger species (DS-PGI) ranged from 165,000 to 285,000. DS-PGI self-associates in 0.375 M Tris, while DS-PGII does not. This phenomenon was exploited to separate DS-PGI and DS-PGII by preparative electrophoresis on 5 to 20% gradient slab gels. The immunological identities of the individual species, DS-PGI and DS-PGII, were examined by enzyme-linked immunosorbent assay using polyclonal antiserum to cartilage-specific proteoglycan monomer from bovine articular cartilage and polyclonal and monoclonal antibodies to DS-PGII. The polyclonal antiserum to cartilage-specific proteoglycan monomer did not react with DS-PGI or DS-PGII, indicating that DS-PGI and DS-PGII possess different core proteins from cartilage-specific proteoglycan monomer. Polyclonal and monoclonal antibodies raised against the mixture of DS-PGI and DS-PGII reacted strongly with DS-PGII, but weakly or not at all with DS-PGI. These results suggest that DS-PGI and DS-PGII possess different core proteins and may represent two different species of dermatan sulfate proteoglycans. |
doi_str_mv | 10.1016/S0021-9258(18)88971-2 |
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On sodium dodecyl sulfate-polyacrylamide gel electrophoresis at low ionic strength in 0.01 M phosphate the dermatan sulfate proteoglycans appeared as a single polydisperse species whose molecular weight ranged from 80,000 to 140,000. The dermatan sulfate proteoglycans eluted as a single peak on Sepharose CL-4B chromatography in 4 M guanidine hydrochloride and showed no tendency to separate into two components. Following chondroitinase AC and ABC digestion, a core protein was obtained whose molecular weight was 45,000. However, what appeared to be a single dermatan sulfate proteoglycan was consistently separated into two species of distinctly different mobilities by sodium dodecyl sulfate-polyacrylamide gel electrophoresis at high ionic strength in 0.375 M Tris. The molecular weight of the smaller species (DS-PGII) ranged from 87,000 to 120,000. The molecular weight of the larger species (DS-PGI) ranged from 165,000 to 285,000. DS-PGI self-associates in 0.375 M Tris, while DS-PGII does not. This phenomenon was exploited to separate DS-PGI and DS-PGII by preparative electrophoresis on 5 to 20% gradient slab gels. The immunological identities of the individual species, DS-PGI and DS-PGII, were examined by enzyme-linked immunosorbent assay using polyclonal antiserum to cartilage-specific proteoglycan monomer from bovine articular cartilage and polyclonal and monoclonal antibodies to DS-PGII. The polyclonal antiserum to cartilage-specific proteoglycan monomer did not react with DS-PGI or DS-PGII, indicating that DS-PGI and DS-PGII possess different core proteins from cartilage-specific proteoglycan monomer. Polyclonal and monoclonal antibodies raised against the mixture of DS-PGI and DS-PGII reacted strongly with DS-PGII, but weakly or not at all with DS-PGI. These results suggest that DS-PGI and DS-PGII possess different core proteins and may represent two different species of dermatan sulfate proteoglycans.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1016/S0021-9258(18)88971-2</identifier><identifier>PMID: 3997823</identifier><identifier>CODEN: JBCHA3</identifier><language>eng</language><publisher>Bethesda, MD: Elsevier Inc</publisher><subject>Analytical, structural and metabolic biochemistry ; Animals ; Antibodies - immunology ; Biological and medical sciences ; Carbohydrates ; Cartilage, Articular - analysis ; Cattle ; Chondroitin - analogs & derivatives ; Chondroitin Sulfate Proteoglycans - immunology ; Chondroitin Sulfate Proteoglycans - isolation & purification ; Chondroitinases and Chondroitin Lyases ; Dermatan Sulfate - immunology ; Dermatan Sulfate - isolation & purification ; Electrophoresis, Polyacrylamide Gel ; Fundamental and applied biological sciences. Psychology ; Immunochemistry ; Molecular Weight ; Other biological molecules ; Proteoglycans - isolation & purification</subject><ispartof>The Journal of biological chemistry, 1985-05, Vol.260 (10), p.6304-6313</ispartof><rights>1985 © 1985 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><rights>1986 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c530t-6a22529403f6d421226e3f8f38527bf9e88f381823b66fdb8a66d83c995f3a833</citedby><cites>FETCH-LOGICAL-c530t-6a22529403f6d421226e3f8f38527bf9e88f381823b66fdb8a66d83c995f3a833</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8473965$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3997823$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rosenberg, L C</creatorcontrib><creatorcontrib>Choi, H U</creatorcontrib><creatorcontrib>Tang, L H</creatorcontrib><creatorcontrib>Johnson, T L</creatorcontrib><creatorcontrib>Pal, S</creatorcontrib><creatorcontrib>Webber, C</creatorcontrib><creatorcontrib>Reiner, A</creatorcontrib><creatorcontrib>Poole, A R</creatorcontrib><title>Isolation of dermatan sulfate proteoglycans from mature bovine articular cartilages</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Two species of dermatan sulfate proteoglycans, called DS-PGI and DS-PGII, have been isolated from mature bovine articular cartilages. On sodium dodecyl sulfate-polyacrylamide gel electrophoresis at low ionic strength in 0.01 M phosphate the dermatan sulfate proteoglycans appeared as a single polydisperse species whose molecular weight ranged from 80,000 to 140,000. The dermatan sulfate proteoglycans eluted as a single peak on Sepharose CL-4B chromatography in 4 M guanidine hydrochloride and showed no tendency to separate into two components. Following chondroitinase AC and ABC digestion, a core protein was obtained whose molecular weight was 45,000. However, what appeared to be a single dermatan sulfate proteoglycan was consistently separated into two species of distinctly different mobilities by sodium dodecyl sulfate-polyacrylamide gel electrophoresis at high ionic strength in 0.375 M Tris. The molecular weight of the smaller species (DS-PGII) ranged from 87,000 to 120,000. The molecular weight of the larger species (DS-PGI) ranged from 165,000 to 285,000. DS-PGI self-associates in 0.375 M Tris, while DS-PGII does not. This phenomenon was exploited to separate DS-PGI and DS-PGII by preparative electrophoresis on 5 to 20% gradient slab gels. The immunological identities of the individual species, DS-PGI and DS-PGII, were examined by enzyme-linked immunosorbent assay using polyclonal antiserum to cartilage-specific proteoglycan monomer from bovine articular cartilage and polyclonal and monoclonal antibodies to DS-PGII. The polyclonal antiserum to cartilage-specific proteoglycan monomer did not react with DS-PGI or DS-PGII, indicating that DS-PGI and DS-PGII possess different core proteins from cartilage-specific proteoglycan monomer. Polyclonal and monoclonal antibodies raised against the mixture of DS-PGI and DS-PGII reacted strongly with DS-PGII, but weakly or not at all with DS-PGI. These results suggest that DS-PGI and DS-PGII possess different core proteins and may represent two different species of dermatan sulfate proteoglycans.</description><subject>Analytical, structural and metabolic biochemistry</subject><subject>Animals</subject><subject>Antibodies - immunology</subject><subject>Biological and medical sciences</subject><subject>Carbohydrates</subject><subject>Cartilage, Articular - analysis</subject><subject>Cattle</subject><subject>Chondroitin - analogs & derivatives</subject><subject>Chondroitin Sulfate Proteoglycans - immunology</subject><subject>Chondroitin Sulfate Proteoglycans - isolation & purification</subject><subject>Chondroitinases and Chondroitin Lyases</subject><subject>Dermatan Sulfate - immunology</subject><subject>Dermatan Sulfate - isolation & purification</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Immunochemistry</subject><subject>Molecular Weight</subject><subject>Other biological molecules</subject><subject>Proteoglycans - isolation & purification</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkF1LHTEQhkNR7KntTxACSqkX2-ZjN5tcSRFbBcELW-hdyGYn56RkN5rsKv57s57DuTU3MzDPmxkehE4o-U4JFT_uCWG0UqyR36g8l1K1tGIf0IoSySve0H8HaLVHPqJPOf8n5dWKHqEjrlQrGV-h-5scg5l8HHF0uIc0mMmMOM_BmQnwQ4oTxHV4sWbM2KU44ALMCXAXn_wI2KTJ2zmYhO3SBrOG_BkdOhMyfNnVY_T319Wfy-vq9u73zeXP28o2nEyVMIw1TNWEO9HXjDImgDvpuGxY2zkFculpObMTwvWdNEL0klulGseN5PwYfd3-W658nCFPevDZQghmhDhn3QrKCa1lAZstaFPMOYHTD8kPJr1oSvQiU7_J1IspTaV-k6lZyZ3sFszdAP0-tbNX5me7ucnWBJfMaH3eY7JuuRJNwU632MavN88-ge58tBsYNBPLfi04qQt1saWgKHvykHS2HkYLfUnYSffRv3PuKyBanJA</recordid><startdate>19850525</startdate><enddate>19850525</enddate><creator>Rosenberg, L C</creator><creator>Choi, H U</creator><creator>Tang, L H</creator><creator>Johnson, T L</creator><creator>Pal, S</creator><creator>Webber, C</creator><creator>Reiner, A</creator><creator>Poole, A R</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19850525</creationdate><title>Isolation of dermatan sulfate proteoglycans from mature bovine articular cartilages</title><author>Rosenberg, L C ; Choi, H U ; Tang, L H ; Johnson, T L ; Pal, S ; Webber, C ; Reiner, A ; Poole, A R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c530t-6a22529403f6d421226e3f8f38527bf9e88f381823b66fdb8a66d83c995f3a833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Analytical, structural and metabolic biochemistry</topic><topic>Animals</topic><topic>Antibodies - immunology</topic><topic>Biological and medical sciences</topic><topic>Carbohydrates</topic><topic>Cartilage, Articular - analysis</topic><topic>Cattle</topic><topic>Chondroitin - analogs & derivatives</topic><topic>Chondroitin Sulfate Proteoglycans - immunology</topic><topic>Chondroitin Sulfate Proteoglycans - isolation & purification</topic><topic>Chondroitinases and Chondroitin Lyases</topic><topic>Dermatan Sulfate - immunology</topic><topic>Dermatan Sulfate - isolation & purification</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Immunochemistry</topic><topic>Molecular Weight</topic><topic>Other biological molecules</topic><topic>Proteoglycans - isolation & purification</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rosenberg, L C</creatorcontrib><creatorcontrib>Choi, H U</creatorcontrib><creatorcontrib>Tang, L H</creatorcontrib><creatorcontrib>Johnson, T L</creatorcontrib><creatorcontrib>Pal, S</creatorcontrib><creatorcontrib>Webber, C</creatorcontrib><creatorcontrib>Reiner, A</creatorcontrib><creatorcontrib>Poole, A R</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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>MEDLINE - Academic</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rosenberg, L C</au><au>Choi, H U</au><au>Tang, L H</au><au>Johnson, T L</au><au>Pal, S</au><au>Webber, C</au><au>Reiner, A</au><au>Poole, A R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Isolation of dermatan sulfate proteoglycans from mature bovine articular cartilages</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>1985-05-25</date><risdate>1985</risdate><volume>260</volume><issue>10</issue><spage>6304</spage><epage>6313</epage><pages>6304-6313</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><coden>JBCHA3</coden><abstract>Two species of dermatan sulfate proteoglycans, called DS-PGI and DS-PGII, have been isolated from mature bovine articular cartilages. On sodium dodecyl sulfate-polyacrylamide gel electrophoresis at low ionic strength in 0.01 M phosphate the dermatan sulfate proteoglycans appeared as a single polydisperse species whose molecular weight ranged from 80,000 to 140,000. The dermatan sulfate proteoglycans eluted as a single peak on Sepharose CL-4B chromatography in 4 M guanidine hydrochloride and showed no tendency to separate into two components. Following chondroitinase AC and ABC digestion, a core protein was obtained whose molecular weight was 45,000. However, what appeared to be a single dermatan sulfate proteoglycan was consistently separated into two species of distinctly different mobilities by sodium dodecyl sulfate-polyacrylamide gel electrophoresis at high ionic strength in 0.375 M Tris. The molecular weight of the smaller species (DS-PGII) ranged from 87,000 to 120,000. The molecular weight of the larger species (DS-PGI) ranged from 165,000 to 285,000. DS-PGI self-associates in 0.375 M Tris, while DS-PGII does not. This phenomenon was exploited to separate DS-PGI and DS-PGII by preparative electrophoresis on 5 to 20% gradient slab gels. The immunological identities of the individual species, DS-PGI and DS-PGII, were examined by enzyme-linked immunosorbent assay using polyclonal antiserum to cartilage-specific proteoglycan monomer from bovine articular cartilage and polyclonal and monoclonal antibodies to DS-PGII. The polyclonal antiserum to cartilage-specific proteoglycan monomer did not react with DS-PGI or DS-PGII, indicating that DS-PGI and DS-PGII possess different core proteins from cartilage-specific proteoglycan monomer. Polyclonal and monoclonal antibodies raised against the mixture of DS-PGI and DS-PGII reacted strongly with DS-PGII, but weakly or not at all with DS-PGI. These results suggest that DS-PGI and DS-PGII possess different core proteins and may represent two different species of dermatan sulfate proteoglycans.</abstract><cop>Bethesda, MD</cop><pub>Elsevier Inc</pub><pmid>3997823</pmid><doi>10.1016/S0021-9258(18)88971-2</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analytical, structural and metabolic biochemistry Animals Antibodies - immunology Biological and medical sciences Carbohydrates Cartilage, Articular - analysis Cattle Chondroitin - analogs & derivatives Chondroitin Sulfate Proteoglycans - immunology Chondroitin Sulfate Proteoglycans - isolation & purification Chondroitinases and Chondroitin Lyases Dermatan Sulfate - immunology Dermatan Sulfate - isolation & purification Electrophoresis, Polyacrylamide Gel Fundamental and applied biological sciences. Psychology Immunochemistry Molecular Weight Other biological molecules Proteoglycans - isolation & purification |
title | Isolation of dermatan sulfate proteoglycans from mature bovine articular cartilages |
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