{"title":"Monoclonal antibody identification of a potentially lithogenic protein extracted from human renal calculi.","authors":"L B Kandel, T C Whyard, M J Gonder","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>In an attempt to identify potentially lithogenic proteins, a detergent soluble extract of human renal calculi was used to produce a unique monoclonal antibody. The monoclonal antibody was found to detect the presence of a specific epitope in 77% of individually extracted kidney stones from our patients' stone bank at The Long Island Kidney Stone Unit, State University of New York, Stony Brook. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis, immunoprecipitation, and Western Blot analysis revealed this monoclonal antibody to be specific to a protein of 83,000 dalton molecular weight. A secondary source of protein reactive to the monoclonal antibody was subjected to enzyme kinetic studies, those studies suggested that the 83,000 dalton protein is a member of the protein-glutamine gammaglutamyltransferase (transglutaminase) family of enzymes. It was not determined in the present investigation whether a member of this family of enzymes initiates or is necessary for lithiasis.</p>","PeriodicalId":80218,"journal":{"name":"The Journal of stone disease","volume":"4 4","pages":"283-8"},"PeriodicalIF":0.0000,"publicationDate":"1992-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of stone disease","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
In an attempt to identify potentially lithogenic proteins, a detergent soluble extract of human renal calculi was used to produce a unique monoclonal antibody. The monoclonal antibody was found to detect the presence of a specific epitope in 77% of individually extracted kidney stones from our patients' stone bank at The Long Island Kidney Stone Unit, State University of New York, Stony Brook. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis, immunoprecipitation, and Western Blot analysis revealed this monoclonal antibody to be specific to a protein of 83,000 dalton molecular weight. A secondary source of protein reactive to the monoclonal antibody was subjected to enzyme kinetic studies, those studies suggested that the 83,000 dalton protein is a member of the protein-glutamine gammaglutamyltransferase (transglutaminase) family of enzymes. It was not determined in the present investigation whether a member of this family of enzymes initiates or is necessary for lithiasis.