Effect of covalent attachment of polyethylene glycol on immunogenicity and circulating life of bovine liver catalase

Methoxypolyethylene glycols of 1900 daltons (PEG-1900) or 5000 daltons (PEG-5000) were covalently attached to bovine liver catalase using 2,4,6-trichloro-s-triazine as the coupling agent. Rabbits were immunized by the intravenous and intramuscular routes with catalase modified by covalent attachment...

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Veröffentlicht in:The Journal of biological chemistry 1977-06, Vol.252 (11), p.3582-3586
Hauptverfasser: Abuchowski, A, McCoy, J R, Palczuk, N C, van Es, T, Davis, F F
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container_end_page 3586
container_issue 11
container_start_page 3582
container_title The Journal of biological chemistry
container_volume 252
creator Abuchowski, A
McCoy, J R
Palczuk, N C
van Es, T
Davis, F F
description Methoxypolyethylene glycols of 1900 daltons (PEG-1900) or 5000 daltons (PEG-5000) were covalently attached to bovine liver catalase using 2,4,6-trichloro-s-triazine as the coupling agent. Rabbits were immunized by the intravenous and intramuscular routes with catalase modified by covalent attachment of PEG-1900 to 43% of the amino groups (PEG-1900-catalase). The intravenous antiserum did not yield detectable antibodies against PEG-1900-catalase or native catalase, as determined by Ouchterlony and complement fixation methods, whereas the intramuscular antiserum contained antibodies to both PEG-1900-catalase and catalase. PEG-1900 did not react with either antiserum. Catalase was prepared in which PEG-5000 was attached to 40% of the amino groups (PEG-5000-catalase). This catalase preparation did not react with either antiserum. PEG-1900-catalase retained 93% of its enzymatic activity; PEG-5000-catalase retained 95%. PEG-5000-catalase resisted digestion by trypsin, chymotrypsin, and a protease from Streptomyces griseus. PEG-1900-catalase and PEG-5000-catalase exhibited enhanced circulating lives in the blood of acatalasemic mice during repetitive intravenous injections. No evidence was seen of an immune response to injections of the modified enzymes. Mice injected repetitively with PEG-5000-catalase remained immune competent for unmodieied catalase, and no evidence of tissue or organ damage was seen.
doi_str_mv 10.1016/s0021-9258(17)40292-4
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Rabbits were immunized by the intravenous and intramuscular routes with catalase modified by covalent attachment of PEG-1900 to 43% of the amino groups (PEG-1900-catalase). The intravenous antiserum did not yield detectable antibodies against PEG-1900-catalase or native catalase, as determined by Ouchterlony and complement fixation methods, whereas the intramuscular antiserum contained antibodies to both PEG-1900-catalase and catalase. PEG-1900 did not react with either antiserum. Catalase was prepared in which PEG-5000 was attached to 40% of the amino groups (PEG-5000-catalase). This catalase preparation did not react with either antiserum. PEG-1900-catalase retained 93% of its enzymatic activity; PEG-5000-catalase retained 95%. PEG-5000-catalase resisted digestion by trypsin, chymotrypsin, and a protease from Streptomyces griseus. PEG-1900-catalase and PEG-5000-catalase exhibited enhanced circulating lives in the blood of acatalasemic mice during repetitive intravenous injections. No evidence was seen of an immune response to injections of the modified enzymes. Mice injected repetitively with PEG-5000-catalase remained immune competent for unmodieied catalase, and no evidence of tissue or organ damage was seen.</description><subject>Acatalasia</subject><subject>Animals</subject><subject>Antibody Formation - drug effects</subject><subject>Catalase - blood</subject><subject>Catalase - immunology</subject><subject>Cattle</subject><subject>Complement Fixation Tests</subject><subject>Hot Temperature</subject><subject>Hydrogen-Ion Concentration</subject><subject>Immunodiffusion</subject><subject>Liver</subject><subject>Mice</subject><subject>Molecular Weight</subject><subject>Peptide Hydrolases</subject><subject>Polyethylene Glycols - pharmacology</subject><subject>Rabbits</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1977</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkF2L1TAQhoO46HH1F4gQEEQvqpkk_cilLOsHLHihgnchTSankbQ5NumR_ntbz6JzM8O87zsDDyEvgL0FBs27zBiHSvG6ew3tG8m44pV8QA7AOlGJGn48JId_lsfkSc4_2VZSwSNyBY1i7YGUW-_RFpo8telsIk6FmlKMHcZ93NanFFcsw7pJSI9xtSnSNNEwjsuUjjgFG8pKzeSoDbNdoilhOtIYPO7pPp3DlovhjDO1pphoMj4lV97EjM_u-zX5_uH2282n6u7Lx8837-8qK1VdKkAnALhqOfS-921rbCNl02LjG-e8c-iMQyOlqZVVHe9FL3lnLbYoOgtCXJNXl7unOf1aMBc9hmwxRjNhWrLuhGpkzdvNWF-Mdk45z-j1aQ6jmVcNTO-s9dcdpN5Bamj1X9Zabrnn9w-WfkT3P7XD3dSXF3UIx-F3mFH3IdkBR81rrgG0qDsu_gB3ZokK</recordid><startdate>19770610</startdate><enddate>19770610</enddate><creator>Abuchowski, A</creator><creator>McCoy, J R</creator><creator>Palczuk, N C</creator><creator>van Es, T</creator><creator>Davis, F F</creator><general>American Society for Biochemistry and Molecular Biology</general><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>19770610</creationdate><title>Effect of covalent attachment of polyethylene glycol on immunogenicity and circulating life of bovine liver catalase</title><author>Abuchowski, A ; McCoy, J R ; Palczuk, N C ; van Es, T ; Davis, F F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c495t-1ed31129721bfbf77ac64467e6f6ddfddedadea44a59c982b3b428cce7e38c133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1977</creationdate><topic>Acatalasia</topic><topic>Animals</topic><topic>Antibody Formation - drug effects</topic><topic>Catalase - blood</topic><topic>Catalase - immunology</topic><topic>Cattle</topic><topic>Complement Fixation Tests</topic><topic>Hot Temperature</topic><topic>Hydrogen-Ion Concentration</topic><topic>Immunodiffusion</topic><topic>Liver</topic><topic>Mice</topic><topic>Molecular Weight</topic><topic>Peptide Hydrolases</topic><topic>Polyethylene Glycols - pharmacology</topic><topic>Rabbits</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abuchowski, A</creatorcontrib><creatorcontrib>McCoy, J R</creatorcontrib><creatorcontrib>Palczuk, N C</creatorcontrib><creatorcontrib>van Es, T</creatorcontrib><creatorcontrib>Davis, F F</creatorcontrib><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>Abuchowski, A</au><au>McCoy, J R</au><au>Palczuk, N C</au><au>van Es, T</au><au>Davis, F F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of covalent attachment of polyethylene glycol on immunogenicity and circulating life of bovine liver catalase</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>1977-06-10</date><risdate>1977</risdate><volume>252</volume><issue>11</issue><spage>3582</spage><epage>3586</epage><pages>3582-3586</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Methoxypolyethylene glycols of 1900 daltons (PEG-1900) or 5000 daltons (PEG-5000) were covalently attached to bovine liver catalase using 2,4,6-trichloro-s-triazine as the coupling agent. Rabbits were immunized by the intravenous and intramuscular routes with catalase modified by covalent attachment of PEG-1900 to 43% of the amino groups (PEG-1900-catalase). The intravenous antiserum did not yield detectable antibodies against PEG-1900-catalase or native catalase, as determined by Ouchterlony and complement fixation methods, whereas the intramuscular antiserum contained antibodies to both PEG-1900-catalase and catalase. PEG-1900 did not react with either antiserum. Catalase was prepared in which PEG-5000 was attached to 40% of the amino groups (PEG-5000-catalase). This catalase preparation did not react with either antiserum. PEG-1900-catalase retained 93% of its enzymatic activity; PEG-5000-catalase retained 95%. PEG-5000-catalase resisted digestion by trypsin, chymotrypsin, and a protease from Streptomyces griseus. PEG-1900-catalase and PEG-5000-catalase exhibited enhanced circulating lives in the blood of acatalasemic mice during repetitive intravenous injections. 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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Acatalasia
Animals
Antibody Formation - drug effects
Catalase - blood
Catalase - immunology
Cattle
Complement Fixation Tests
Hot Temperature
Hydrogen-Ion Concentration
Immunodiffusion
Liver
Mice
Molecular Weight
Peptide Hydrolases
Polyethylene Glycols - pharmacology
Rabbits
title Effect of covalent attachment of polyethylene glycol on immunogenicity and circulating life of bovine liver catalase
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