Mapping the Binding Domain of Immunoglobulin Light Chains for Tamm-Horsfall Protein
Cast nephropathy, or myeloma kidney, is a potentially reversible cause of chronic renal failure. In this condition, filtered light chains bind to a common site on Tamm-Horsfall protein (THP), which is produced by cells of the thick ascending limb of the loop of Henle. Subsequent aggregation of these...
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Veröffentlicht in: | The American journal of pathology 2001-05, Vol.158 (5), p.1859-1866 |
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description | Cast nephropathy, or myeloma kidney, is a potentially reversible cause of chronic renal failure. In this condition, filtered light chains bind to a common site on Tamm-Horsfall protein (THP), which is produced by cells of the thick ascending limb of the loop of Henle. Subsequent aggregation of these proteins produces casts that obstruct tubule fluid flow and results in renal failure. In the present study, we used the yeast two-hybrid system to determine the site of interaction of light chains with THP. The third complementarity-determining region (CDR3) of both κ and λ light chains interacted with THP. These findings were confirmed in a series of competition studies using a synthetic peptide that corresponded to the CDR3 region and purified THP and light chains. Variations in the CDR3 sequence of the light chain affected binding. Thus, the current studies increase our understanding of the process of cast formation and provide an opportunity to develop strategies that may inhibit this interaction and prevent the clinical manifestations of myeloma kidney. |
doi_str_mv | 10.1016/S0002-9440(10)64142-9 |
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In this condition, filtered light chains bind to a common site on Tamm-Horsfall protein (THP), which is produced by cells of the thick ascending limb of the loop of Henle. Subsequent aggregation of these proteins produces casts that obstruct tubule fluid flow and results in renal failure. In the present study, we used the yeast two-hybrid system to determine the site of interaction of light chains with THP. The third complementarity-determining region (CDR3) of both κ and λ light chains interacted with THP. These findings were confirmed in a series of competition studies using a synthetic peptide that corresponded to the CDR3 region and purified THP and light chains. Variations in the CDR3 sequence of the light chain affected binding. Thus, the current studies increase our understanding of the process of cast formation and provide an opportunity to develop strategies that may inhibit this interaction and prevent the clinical manifestations of myeloma kidney.</description><identifier>ISSN: 0002-9440</identifier><identifier>EISSN: 1525-2191</identifier><identifier>DOI: 10.1016/S0002-9440(10)64142-9</identifier><identifier>PMID: 11337384</identifier><identifier>CODEN: AJPAA4</identifier><language>eng</language><publisher>Bethesda, MD: Elsevier Inc</publisher><subject>Binding Sites ; Binding, Competitive ; Biological and medical sciences ; Complementarity Determining Regions - genetics ; Complementarity Determining Regions - metabolism ; Epitope Mapping ; Hematologic and hematopoietic diseases ; Humans ; Immunoglobulin Light Chains - genetics ; Immunoglobulin Light Chains - metabolism ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Medical sciences ; Mucoproteins - genetics ; Mucoproteins - metabolism ; Oligopeptides - chemical synthesis ; Oligopeptides - metabolism ; Protein Binding ; Regular ; Saccharomyces cerevisiae - genetics ; Two-Hybrid System Techniques ; Uromodulin</subject><ispartof>The American journal of pathology, 2001-05, Vol.158 (5), p.1859-1866</ispartof><rights>2001 American Society for Investigative Pathology</rights><rights>2001 INIST-CNRS</rights><rights>Copyright American Society for Investigative Pathology May 2001</rights><rights>Copyright © 2001, American Society for Investigative Pathology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c551t-eb726571a83ef3259ac50154cbed190619689c5061663ef3e98cf64697906a4d3</citedby><cites>FETCH-LOGICAL-c551t-eb726571a83ef3259ac50154cbed190619689c5061663ef3e98cf64697906a4d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1891942/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0002944010641429$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3537,27901,27902,53766,53768,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1065073$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11337384$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ying, Wei-Zhong</creatorcontrib><creatorcontrib>Sanders, Paul W.</creatorcontrib><title>Mapping the Binding Domain of Immunoglobulin Light Chains for Tamm-Horsfall Protein</title><title>The American journal of pathology</title><addtitle>Am J Pathol</addtitle><description>Cast nephropathy, or myeloma kidney, is a potentially reversible cause of chronic renal failure. In this condition, filtered light chains bind to a common site on Tamm-Horsfall protein (THP), which is produced by cells of the thick ascending limb of the loop of Henle. Subsequent aggregation of these proteins produces casts that obstruct tubule fluid flow and results in renal failure. In the present study, we used the yeast two-hybrid system to determine the site of interaction of light chains with THP. The third complementarity-determining region (CDR3) of both κ and λ light chains interacted with THP. These findings were confirmed in a series of competition studies using a synthetic peptide that corresponded to the CDR3 region and purified THP and light chains. Variations in the CDR3 sequence of the light chain affected binding. Thus, the current studies increase our understanding of the process of cast formation and provide an opportunity to develop strategies that may inhibit this interaction and prevent the clinical manifestations of myeloma kidney.</description><subject>Binding Sites</subject><subject>Binding, Competitive</subject><subject>Biological and medical sciences</subject><subject>Complementarity Determining Regions - genetics</subject><subject>Complementarity Determining Regions - metabolism</subject><subject>Epitope Mapping</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Immunoglobulin Light Chains - genetics</subject><subject>Immunoglobulin Light Chains - metabolism</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. 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In this condition, filtered light chains bind to a common site on Tamm-Horsfall protein (THP), which is produced by cells of the thick ascending limb of the loop of Henle. Subsequent aggregation of these proteins produces casts that obstruct tubule fluid flow and results in renal failure. In the present study, we used the yeast two-hybrid system to determine the site of interaction of light chains with THP. The third complementarity-determining region (CDR3) of both κ and λ light chains interacted with THP. These findings were confirmed in a series of competition studies using a synthetic peptide that corresponded to the CDR3 region and purified THP and light chains. Variations in the CDR3 sequence of the light chain affected binding. Thus, the current studies increase our understanding of the process of cast formation and provide an opportunity to develop strategies that may inhibit this interaction and prevent the clinical manifestations of myeloma kidney.</abstract><cop>Bethesda, MD</cop><pub>Elsevier Inc</pub><pmid>11337384</pmid><doi>10.1016/S0002-9440(10)64142-9</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Binding Sites Binding, Competitive Biological and medical sciences Complementarity Determining Regions - genetics Complementarity Determining Regions - metabolism Epitope Mapping Hematologic and hematopoietic diseases Humans Immunoglobulin Light Chains - genetics Immunoglobulin Light Chains - metabolism Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Medical sciences Mucoproteins - genetics Mucoproteins - metabolism Oligopeptides - chemical synthesis Oligopeptides - metabolism Protein Binding Regular Saccharomyces cerevisiae - genetics Two-Hybrid System Techniques Uromodulin |
title | Mapping the Binding Domain of Immunoglobulin Light Chains for Tamm-Horsfall Protein |
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