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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The American journal of pathology 2001-05, Vol.158 (5), p.1859-1866
Hauptverfasser: Ying, Wei-Zhong, Sanders, Paul W.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1866
container_issue 5
container_start_page 1859
container_title The American journal of pathology
container_volume 158
creator Ying, Wei-Zhong
Sanders, Paul W.
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
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1891942</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0002944010641429</els_id><sourcerecordid>73093097</sourcerecordid><originalsourceid>FETCH-LOGICAL-c551t-eb726571a83ef3259ac50154cbed190619689c5061663ef3e98cf64697906a4d3</originalsourceid><addsrcrecordid>eNqFkU1v1DAQhi0EokvhJ4AiVPFxCHgS24kvIFg-WmkRSC1ny-s4u14ldrCTVv33TLqrUrhwsmfmmXdm9BLyFOgboCDenlNKi1wyRl8BfS0YMIzukQXwgucFSLhPFrfIEXmU0g5DUdb0ITkCKMuqrNmCnH_Tw-D8Jhu3NvvofDP_P4VeO5-FNjvr-8mHTRfWU4eZldtsx2y5xWrK2hCzC933-WmIqdVdl_2IYbTOPyYPMEz2yeE9Jj-_fL5Ynuar71_Plh9WueEcxtyuq0LwCnRd2rYsuNSGU-DMrG0DkgqQopaYEiDETFhZm1YwISssataUx-TdXneY1r1tjPVj1J0aout1vFZBO_V3xbut2oRLBbUEyQoUeHEQiOHXZNOoepeM7TrtbZiSqmhdVELM4PN_wF2YosfjVIFiXAjJEOJ7yMSQUrTt7SZA1eyZuvFMzYbMqRvPlMS-Z3fP-NN1MAmBkwOgk9FdG7U3Lt1RF5xWJWIv99gWXbpy0arUoyuoCkrvBuC14ng6nye-35MW3bl0NqpknPXGNthlRtUE95-dfwPjaL9n</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>218956694</pqid></control><display><type>article</type><title>Mapping the Binding Domain of Immunoglobulin Light Chains for Tamm-Horsfall Protein</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>Ying, Wei-Zhong ; Sanders, Paul W.</creator><creatorcontrib>Ying, Wei-Zhong ; Sanders, Paul W.</creatorcontrib><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><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&amp;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. Myelofibrosis</subject><subject>Medical sciences</subject><subject>Mucoproteins - genetics</subject><subject>Mucoproteins - metabolism</subject><subject>Oligopeptides - chemical synthesis</subject><subject>Oligopeptides - metabolism</subject><subject>Protein Binding</subject><subject>Regular</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Two-Hybrid System Techniques</subject><subject>Uromodulin</subject><issn>0002-9440</issn><issn>1525-2191</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkU1v1DAQhi0EokvhJ4AiVPFxCHgS24kvIFg-WmkRSC1ny-s4u14ldrCTVv33TLqrUrhwsmfmmXdm9BLyFOgboCDenlNKi1wyRl8BfS0YMIzukQXwgucFSLhPFrfIEXmU0g5DUdb0ITkCKMuqrNmCnH_Tw-D8Jhu3NvvofDP_P4VeO5-FNjvr-8mHTRfWU4eZldtsx2y5xWrK2hCzC933-WmIqdVdl_2IYbTOPyYPMEz2yeE9Jj-_fL5Ynuar71_Plh9WueEcxtyuq0LwCnRd2rYsuNSGU-DMrG0DkgqQopaYEiDETFhZm1YwISssataUx-TdXneY1r1tjPVj1J0aout1vFZBO_V3xbut2oRLBbUEyQoUeHEQiOHXZNOoepeM7TrtbZiSqmhdVELM4PN_wF2YosfjVIFiXAjJEOJ7yMSQUrTt7SZA1eyZuvFMzYbMqRvPlMS-Z3fP-NN1MAmBkwOgk9FdG7U3Lt1RF5xWJWIv99gWXbpy0arUoyuoCkrvBuC14ng6nye-35MW3bl0NqpknPXGNthlRtUE95-dfwPjaL9n</recordid><startdate>20010501</startdate><enddate>20010501</enddate><creator>Ying, Wei-Zhong</creator><creator>Sanders, Paul W.</creator><general>Elsevier Inc</general><general>ASIP</general><general>American Society for Investigative Pathology</general><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20010501</creationdate><title>Mapping the Binding Domain of Immunoglobulin Light Chains for Tamm-Horsfall Protein</title><author>Ying, Wei-Zhong ; Sanders, Paul W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c551t-eb726571a83ef3259ac50154cbed190619689c5061663ef3e98cf64697906a4d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Binding Sites</topic><topic>Binding, Competitive</topic><topic>Biological and medical sciences</topic><topic>Complementarity Determining Regions - genetics</topic><topic>Complementarity Determining Regions - metabolism</topic><topic>Epitope Mapping</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>Immunoglobulin Light Chains - genetics</topic><topic>Immunoglobulin Light Chains - metabolism</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Medical sciences</topic><topic>Mucoproteins - genetics</topic><topic>Mucoproteins - metabolism</topic><topic>Oligopeptides - chemical synthesis</topic><topic>Oligopeptides - metabolism</topic><topic>Protein Binding</topic><topic>Regular</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Two-Hybrid System Techniques</topic><topic>Uromodulin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ying, Wei-Zhong</creatorcontrib><creatorcontrib>Sanders, Paul W.</creatorcontrib><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>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The American journal of pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ying, Wei-Zhong</au><au>Sanders, Paul W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mapping the Binding Domain of Immunoglobulin Light Chains for Tamm-Horsfall Protein</atitle><jtitle>The American journal of pathology</jtitle><addtitle>Am J Pathol</addtitle><date>2001-05-01</date><risdate>2001</risdate><volume>158</volume><issue>5</issue><spage>1859</spage><epage>1866</epage><pages>1859-1866</pages><issn>0002-9440</issn><eissn>1525-2191</eissn><coden>AJPAA4</coden><abstract>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.</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>
fulltext fulltext
identifier ISSN: 0002-9440
ispartof The American journal of pathology, 2001-05, Vol.158 (5), p.1859-1866
issn 0002-9440
1525-2191
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1891942
source MEDLINE; Elsevier ScienceDirect Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-03T07%3A39%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Mapping%20the%20Binding%20Domain%20of%20Immunoglobulin%20Light%20Chains%20for%20Tamm-Horsfall%20Protein&rft.jtitle=The%20American%20journal%20of%20pathology&rft.au=Ying,%20Wei-Zhong&rft.date=2001-05-01&rft.volume=158&rft.issue=5&rft.spage=1859&rft.epage=1866&rft.pages=1859-1866&rft.issn=0002-9440&rft.eissn=1525-2191&rft.coden=AJPAA4&rft_id=info:doi/10.1016/S0002-9440(10)64142-9&rft_dat=%3Cproquest_pubme%3E73093097%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=218956694&rft_id=info:pmid/11337384&rft_els_id=S0002944010641429&rfr_iscdi=true