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The Complex Multimeric Composition of Factor VIII/von Willebrand Factor
We have analyzed the multimeric structure of factor VIII/von Willebrand factor in plasma by sodium dodecyl sulfate electrophoresis using gels of varying porosity and a discontinuous buffer system. Factor VIII/von Willebrand factor bands were identified by reaction with 125l-labeled affinity-purified...
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Published in: | Blood 1981-06, Vol.57 (6), p.1140-1143 |
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description | We have analyzed the multimeric structure of factor VIII/von Willebrand factor in plasma by sodium dodecyl sulfate electrophoresis using gels of varying porosity and a discontinuous buffer system. Factor VIII/von Willebrand factor bands were identified by reaction with 125l-labeled affinity-purified antibody and subsequent autoradiography. In 1% agarose gels, normal plasma displayed a series of sharply defined oligomers. However, increasing the agarose concentration to 2.0% or utilizing mixtures of 0.8% agarose-1.75% acrylamide revealed two bands of lesser intensity interposed between the major bands. When the acrylamide concentration in the gels was increased to 2.5%, bands with a faster mobility than IgM and fibronectin were now evident. Type IIA von Willebrand’s disease showed not only an absence of the larger multimers but also a relative increase in several of the newly identified bands as compared to type IIB, type I, and normal. These studies suggest that factor VIII/von Willebrand factor in IIA von Willebrand’s disease is structurally different from that in other forms of the disorder. They also indicate that the multimeric composition of factor VIII/von Willebrand factor is more complex than can be explained by simple linear polymerization of a single protomer. |
doi_str_mv | 10.1182/blood.V57.6.1140.1140 |
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Factor VIII/von Willebrand factor bands were identified by reaction with 125l-labeled affinity-purified antibody and subsequent autoradiography. In 1% agarose gels, normal plasma displayed a series of sharply defined oligomers. However, increasing the agarose concentration to 2.0% or utilizing mixtures of 0.8% agarose-1.75% acrylamide revealed two bands of lesser intensity interposed between the major bands. When the acrylamide concentration in the gels was increased to 2.5%, bands with a faster mobility than IgM and fibronectin were now evident. Type IIA von Willebrand’s disease showed not only an absence of the larger multimers but also a relative increase in several of the newly identified bands as compared to type IIB, type I, and normal. These studies suggest that factor VIII/von Willebrand factor in IIA von Willebrand’s disease is structurally different from that in other forms of the disorder. 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They also indicate that the multimeric composition of factor VIII/von Willebrand factor is more complex than can be explained by simple linear polymerization of a single protomer.</description><subject>Blood Coagulation Factors</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Factor VIII</subject><subject>Humans</subject><subject>Immunoglobulin M</subject><subject>Molecular Weight</subject><subject>Polymers</subject><subject>von Willebrand Factor</subject><issn>0006-4971</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1981</creationdate><recordtype>article</recordtype><recordid>eNqFkDFPwzAQhS0EKqXwEyplYktrO7bjTAhVtEQqYilltBLnIoySuNhJBf-eNI1YWe6k9-7u6T6E5gQvCJF0mVfWFos9jxeiFxgeygWaEk5liDHFl2iKMRYhS2JyjW68_8SYsIjyCZqIWLI4YVO02X1AsLL1oYLv4KWrWlODM3qQrDetsU1gy2Cd6da6YJ-m6fLYS--mqiB3WVOM1i26KrPKw93YZ-ht_bRbPYfb1026etyGOpISh1GMJdBIMCpoIogkmhSSYN7rGeSY5RGnRRxpyMtEa0LKQoqERknGY0oYF9EM3Z_vHpz96sC3qjZeQ1VlDdjOq5gLKhLG-kF-HtTOeu-gVAdn6sz9KILVCaAaAKoeoBLqxG4o_d58DOjyGoq_rZFY7z-cfei_PBpwymsDjYbCONCtKqz5J-EXU2iAkA</recordid><startdate>198106</startdate><enddate>198106</enddate><creator>Ruggeri, Zaverio M.</creator><creator>Zimmerman, Theodore S.</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</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>198106</creationdate><title>The Complex Multimeric Composition of Factor VIII/von Willebrand Factor</title><author>Ruggeri, Zaverio M. ; Zimmerman, Theodore S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3880-3708e236426296181c1d8105370aeb04b352d73cebf9cc11fd869239a57214563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1981</creationdate><topic>Blood Coagulation Factors</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Factor VIII</topic><topic>Humans</topic><topic>Immunoglobulin M</topic><topic>Molecular Weight</topic><topic>Polymers</topic><topic>von Willebrand Factor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ruggeri, Zaverio M.</creatorcontrib><creatorcontrib>Zimmerman, Theodore S.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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>Blood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ruggeri, Zaverio M.</au><au>Zimmerman, Theodore S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Complex Multimeric Composition of Factor VIII/von Willebrand Factor</atitle><jtitle>Blood</jtitle><addtitle>Blood</addtitle><date>1981-06</date><risdate>1981</risdate><volume>57</volume><issue>6</issue><spage>1140</spage><epage>1143</epage><pages>1140-1143</pages><issn>0006-4971</issn><eissn>1528-0020</eissn><abstract>We have analyzed the multimeric structure of factor VIII/von Willebrand factor in plasma by sodium dodecyl sulfate electrophoresis using gels of varying porosity and a discontinuous buffer system. Factor VIII/von Willebrand factor bands were identified by reaction with 125l-labeled affinity-purified antibody and subsequent autoradiography. In 1% agarose gels, normal plasma displayed a series of sharply defined oligomers. However, increasing the agarose concentration to 2.0% or utilizing mixtures of 0.8% agarose-1.75% acrylamide revealed two bands of lesser intensity interposed between the major bands. When the acrylamide concentration in the gels was increased to 2.5%, bands with a faster mobility than IgM and fibronectin were now evident. Type IIA von Willebrand’s disease showed not only an absence of the larger multimers but also a relative increase in several of the newly identified bands as compared to type IIB, type I, and normal. These studies suggest that factor VIII/von Willebrand factor in IIA von Willebrand’s disease is structurally different from that in other forms of the disorder. 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subjects | Blood Coagulation Factors Electrophoresis, Polyacrylamide Gel Factor VIII Humans Immunoglobulin M Molecular Weight Polymers von Willebrand Factor |
title | The Complex Multimeric Composition of Factor VIII/von Willebrand Factor |
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