Site-directed Mutagenesis Reveals Regions Implicated in the Stability and Fiber Formation of Human λ3r Light Chains
Light chain amyloidosis (AL) is a disease that affects vital organs by the fibrillar aggregation of monoclonal light chains. λ3r germ line is significantly implicated in this disease. In this work, we contrasted the thermodynamic stability and aggregation propensity of 3mJL2 (nonamyloidogenic) and 3...
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creator | Villalba, Miryam I. Canul-Tec, Juan C. Luna-Martínez, Oscar D. Sánchez-Alcalá, Rosalba Olamendi-Portugal, Timoteo Rudiño-Piñera, Enrique Rojas, Sonia Sánchez-López, Rosana Fernández-Velasco, Daniel A. Becerril, Baltazar |
description | Light chain amyloidosis (AL) is a disease that affects vital organs by the fibrillar aggregation of monoclonal light chains. λ3r germ line is significantly implicated in this disease. In this work, we contrasted the thermodynamic stability and aggregation propensity of 3mJL2 (nonamyloidogenic) and 3rJL2 (amyloidogenic) λ3 germ lines. Because of an inherent limitation (extremely low expression), Cys at position 34 of the 3r germ line was replaced by Tyr reaching a good expression yield. A second substitution (W91A) was introduced in 3r to obtain a better template to incorporate additional mutations. Although the single mutant (C34Y) was not fibrillogenic, the second mutation located at CDR3 (W91A) induced fibrillogenesis. We propose, for the first time, that CDR3 (position 91) affects the stability and fiber formation of human λ3r light chains. Using the double mutant (3rJL2/YA) as template, other variants were constructed to evaluate the importance of those substitutions into the stability and aggregation propensity of λ3 light chains. A change in position 7 (P7D) boosted 3rJL2/YA fibrillogenic properties. Modification of position 48 (I48M) partially reverted 3rJL2/YA fibril aggregation. Finally, changes at positions 8 (P8S) or 40 (P40S) completely reverted fibril formation. These results confirm the influential roles of N-terminal region (positions 7 and 8) and the loop 40–60 (positions 40 and 48) on AL. X-ray crystallography revealed that the three-dimensional topology of the single and double λ3r mutants was not significantly altered. This mutagenic approach helped to identify key regions implicated in λ3 AL.
Background: λ6a and λ3r are the most implicated germ lines in light chain amyloidosis.
Results: Mutagenesis at N-terminal, loop 40–60, and CDR3 regions affected λ3r fibrillogenesis.
Conclusion: Changes at residues 7, 48, and 91 increased fibril formation while changes at residues 8 and 40 reverted fibrillogenesis.
Significance: Characterization of light chain germ lines helps to identify key regions implicated in amyloidosis. |
doi_str_mv | 10.1074/jbc.M114.629550 |
format | Article |
fullrecord | <record><control><sourceid>pubmed_osti_</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4317031</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0021925820492361</els_id><sourcerecordid>25505244</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3850-89fe8c425b5ab7e4127af76894c42b55a7cbe3baf8acaadadad22e4969680bcf3</originalsourceid><addsrcrecordid>eNp1kc1qGzEUhUVpady06-6K6H4c_XpGm0IxcRNwCDQJdCckzR2PgkdjJNmQZ-s79JmqYdrQLiItLlx991xxDkIfKVlSUouLR-uWN5SK5YopKckrtKCk4RWX9MdrtCCE0Uox2Zyhdyk9knKEom_RGSusZEIsUL7zGarWR3AZWnxzzGYHAZJP-DucwOynuvNjSPh6OOy9MxPmA8494LtsrN_7_IRNaPHGW4h4M8bB5DKAxw5fHQcT8K-fPOKt3_UZr3vjQ3qP3nRFGT78qefoYXN5v76qtrffrtdft5XjjSRVozponGDSSmNrEJTVpqtXjRKlaaU0tbPAreka44xpp8sYCLVSq4ZY1_Fz9GXWPRztAK2DkKPZ60P0g4lPejRe__8SfK9340kLTmvCaRH4PAuMKXudXPHK9W4MobilKReKSFKgixlycUwpQve8gBI9paRLSnpKSc8plYlP__7rmf8bSwHUDEBx5-QhTrshOJiD0u3oXxT_DTKVpKA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Site-directed Mutagenesis Reveals Regions Implicated in the Stability and Fiber Formation of Human λ3r Light Chains</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Villalba, Miryam I. ; Canul-Tec, Juan C. ; Luna-Martínez, Oscar D. ; Sánchez-Alcalá, Rosalba ; Olamendi-Portugal, Timoteo ; Rudiño-Piñera, Enrique ; Rojas, Sonia ; Sánchez-López, Rosana ; Fernández-Velasco, Daniel A. ; Becerril, Baltazar</creator><creatorcontrib>Villalba, Miryam I. ; Canul-Tec, Juan C. ; Luna-Martínez, Oscar D. ; Sánchez-Alcalá, Rosalba ; Olamendi-Portugal, Timoteo ; Rudiño-Piñera, Enrique ; Rojas, Sonia ; Sánchez-López, Rosana ; Fernández-Velasco, Daniel A. ; Becerril, Baltazar ; National Autonomous Univ. of Mexico, Mexico City (Mexico)</creatorcontrib><description>Light chain amyloidosis (AL) is a disease that affects vital organs by the fibrillar aggregation of monoclonal light chains. λ3r germ line is significantly implicated in this disease. In this work, we contrasted the thermodynamic stability and aggregation propensity of 3mJL2 (nonamyloidogenic) and 3rJL2 (amyloidogenic) λ3 germ lines. Because of an inherent limitation (extremely low expression), Cys at position 34 of the 3r germ line was replaced by Tyr reaching a good expression yield. A second substitution (W91A) was introduced in 3r to obtain a better template to incorporate additional mutations. Although the single mutant (C34Y) was not fibrillogenic, the second mutation located at CDR3 (W91A) induced fibrillogenesis. We propose, for the first time, that CDR3 (position 91) affects the stability and fiber formation of human λ3r light chains. Using the double mutant (3rJL2/YA) as template, other variants were constructed to evaluate the importance of those substitutions into the stability and aggregation propensity of λ3 light chains. A change in position 7 (P7D) boosted 3rJL2/YA fibrillogenic properties. Modification of position 48 (I48M) partially reverted 3rJL2/YA fibril aggregation. Finally, changes at positions 8 (P8S) or 40 (P40S) completely reverted fibril formation. These results confirm the influential roles of N-terminal region (positions 7 and 8) and the loop 40–60 (positions 40 and 48) on AL. X-ray crystallography revealed that the three-dimensional topology of the single and double λ3r mutants was not significantly altered. This mutagenic approach helped to identify key regions implicated in λ3 AL.
Background: λ6a and λ3r are the most implicated germ lines in light chain amyloidosis.
Results: Mutagenesis at N-terminal, loop 40–60, and CDR3 regions affected λ3r fibrillogenesis.
Conclusion: Changes at residues 7, 48, and 91 increased fibril formation while changes at residues 8 and 40 reverted fibrillogenesis.
Significance: Characterization of light chain germ lines helps to identify key regions implicated in amyloidosis.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M114.629550</identifier><identifier>PMID: 25505244</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>60 APPLIED LIFE SCIENCES ; Amino Acid Sequence ; Amyloid ; Amyloidosis - metabolism ; Antibody ; BASIC BIOLOGICAL SCIENCES ; Crystallography, X-Ray ; Fibril ; Humans ; Immunoglobulin lambda-Chains - chemistry ; Immunoglobulin lambda-Chains - metabolism ; Immunoglobulin Light Chains - chemistry ; Immunoglobulin Light Chains - metabolism ; Mutagenesis in Vitro ; Mutagenesis, Site-Directed - methods ; Protein Denaturation ; Protein Structure and Folding ; Protein Structure, Secondary ; Protein Structure, Tertiary ; Thermodynamics</subject><ispartof>The Journal of biological chemistry, 2015-01, Vol.290 (5), p.2577-2592</ispartof><rights>2015 © 2015 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><rights>2015 by The American Society for Biochemistry and Molecular Biology, Inc.</rights><rights>2015 by The American Society for Biochemistry and Molecular Biology, Inc. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3850-89fe8c425b5ab7e4127af76894c42b55a7cbe3baf8acaadadad22e4969680bcf3</citedby><cites>FETCH-LOGICAL-c3850-89fe8c425b5ab7e4127af76894c42b55a7cbe3baf8acaadadad22e4969680bcf3</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/PMC4317031/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4317031/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,725,778,782,883,27911,27912,53778,53780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25505244$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/servlets/purl/1349050$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Villalba, Miryam I.</creatorcontrib><creatorcontrib>Canul-Tec, Juan C.</creatorcontrib><creatorcontrib>Luna-Martínez, Oscar D.</creatorcontrib><creatorcontrib>Sánchez-Alcalá, Rosalba</creatorcontrib><creatorcontrib>Olamendi-Portugal, Timoteo</creatorcontrib><creatorcontrib>Rudiño-Piñera, Enrique</creatorcontrib><creatorcontrib>Rojas, Sonia</creatorcontrib><creatorcontrib>Sánchez-López, Rosana</creatorcontrib><creatorcontrib>Fernández-Velasco, Daniel A.</creatorcontrib><creatorcontrib>Becerril, Baltazar</creatorcontrib><creatorcontrib>National Autonomous Univ. of Mexico, Mexico City (Mexico)</creatorcontrib><title>Site-directed Mutagenesis Reveals Regions Implicated in the Stability and Fiber Formation of Human λ3r Light Chains</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Light chain amyloidosis (AL) is a disease that affects vital organs by the fibrillar aggregation of monoclonal light chains. λ3r germ line is significantly implicated in this disease. In this work, we contrasted the thermodynamic stability and aggregation propensity of 3mJL2 (nonamyloidogenic) and 3rJL2 (amyloidogenic) λ3 germ lines. Because of an inherent limitation (extremely low expression), Cys at position 34 of the 3r germ line was replaced by Tyr reaching a good expression yield. A second substitution (W91A) was introduced in 3r to obtain a better template to incorporate additional mutations. Although the single mutant (C34Y) was not fibrillogenic, the second mutation located at CDR3 (W91A) induced fibrillogenesis. We propose, for the first time, that CDR3 (position 91) affects the stability and fiber formation of human λ3r light chains. Using the double mutant (3rJL2/YA) as template, other variants were constructed to evaluate the importance of those substitutions into the stability and aggregation propensity of λ3 light chains. A change in position 7 (P7D) boosted 3rJL2/YA fibrillogenic properties. Modification of position 48 (I48M) partially reverted 3rJL2/YA fibril aggregation. Finally, changes at positions 8 (P8S) or 40 (P40S) completely reverted fibril formation. These results confirm the influential roles of N-terminal region (positions 7 and 8) and the loop 40–60 (positions 40 and 48) on AL. X-ray crystallography revealed that the three-dimensional topology of the single and double λ3r mutants was not significantly altered. This mutagenic approach helped to identify key regions implicated in λ3 AL.
Background: λ6a and λ3r are the most implicated germ lines in light chain amyloidosis.
Results: Mutagenesis at N-terminal, loop 40–60, and CDR3 regions affected λ3r fibrillogenesis.
Conclusion: Changes at residues 7, 48, and 91 increased fibril formation while changes at residues 8 and 40 reverted fibrillogenesis.
Significance: Characterization of light chain germ lines helps to identify key regions implicated in amyloidosis.</description><subject>60 APPLIED LIFE SCIENCES</subject><subject>Amino Acid Sequence</subject><subject>Amyloid</subject><subject>Amyloidosis - metabolism</subject><subject>Antibody</subject><subject>BASIC BIOLOGICAL SCIENCES</subject><subject>Crystallography, X-Ray</subject><subject>Fibril</subject><subject>Humans</subject><subject>Immunoglobulin lambda-Chains - chemistry</subject><subject>Immunoglobulin lambda-Chains - metabolism</subject><subject>Immunoglobulin Light Chains - chemistry</subject><subject>Immunoglobulin Light Chains - metabolism</subject><subject>Mutagenesis in Vitro</subject><subject>Mutagenesis, Site-Directed - methods</subject><subject>Protein Denaturation</subject><subject>Protein Structure and Folding</subject><subject>Protein Structure, Secondary</subject><subject>Protein Structure, Tertiary</subject><subject>Thermodynamics</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1qGzEUhUVpady06-6K6H4c_XpGm0IxcRNwCDQJdCckzR2PgkdjJNmQZ-s79JmqYdrQLiItLlx991xxDkIfKVlSUouLR-uWN5SK5YopKckrtKCk4RWX9MdrtCCE0Uox2Zyhdyk9knKEom_RGSusZEIsUL7zGarWR3AZWnxzzGYHAZJP-DucwOynuvNjSPh6OOy9MxPmA8494LtsrN_7_IRNaPHGW4h4M8bB5DKAxw5fHQcT8K-fPOKt3_UZr3vjQ3qP3nRFGT78qefoYXN5v76qtrffrtdft5XjjSRVozponGDSSmNrEJTVpqtXjRKlaaU0tbPAreka44xpp8sYCLVSq4ZY1_Fz9GXWPRztAK2DkKPZ60P0g4lPejRe__8SfK9340kLTmvCaRH4PAuMKXudXPHK9W4MobilKReKSFKgixlycUwpQve8gBI9paRLSnpKSc8plYlP__7rmf8bSwHUDEBx5-QhTrshOJiD0u3oXxT_DTKVpKA</recordid><startdate>20150130</startdate><enddate>20150130</enddate><creator>Villalba, Miryam I.</creator><creator>Canul-Tec, Juan C.</creator><creator>Luna-Martínez, Oscar D.</creator><creator>Sánchez-Alcalá, Rosalba</creator><creator>Olamendi-Portugal, Timoteo</creator><creator>Rudiño-Piñera, Enrique</creator><creator>Rojas, Sonia</creator><creator>Sánchez-López, Rosana</creator><creator>Fernández-Velasco, Daniel A.</creator><creator>Becerril, Baltazar</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</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>OIOZB</scope><scope>OTOTI</scope><scope>5PM</scope></search><sort><creationdate>20150130</creationdate><title>Site-directed Mutagenesis Reveals Regions Implicated in the Stability and Fiber Formation of Human λ3r Light Chains</title><author>Villalba, Miryam I. ; Canul-Tec, Juan C. ; Luna-Martínez, Oscar D. ; Sánchez-Alcalá, Rosalba ; Olamendi-Portugal, Timoteo ; Rudiño-Piñera, Enrique ; Rojas, Sonia ; Sánchez-López, Rosana ; Fernández-Velasco, Daniel A. ; Becerril, Baltazar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3850-89fe8c425b5ab7e4127af76894c42b55a7cbe3baf8acaadadad22e4969680bcf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>60 APPLIED LIFE SCIENCES</topic><topic>Amino Acid Sequence</topic><topic>Amyloid</topic><topic>Amyloidosis - metabolism</topic><topic>Antibody</topic><topic>BASIC BIOLOGICAL SCIENCES</topic><topic>Crystallography, X-Ray</topic><topic>Fibril</topic><topic>Humans</topic><topic>Immunoglobulin lambda-Chains - chemistry</topic><topic>Immunoglobulin lambda-Chains - metabolism</topic><topic>Immunoglobulin Light Chains - chemistry</topic><topic>Immunoglobulin Light Chains - metabolism</topic><topic>Mutagenesis in Vitro</topic><topic>Mutagenesis, Site-Directed - methods</topic><topic>Protein Denaturation</topic><topic>Protein Structure and Folding</topic><topic>Protein Structure, Secondary</topic><topic>Protein Structure, Tertiary</topic><topic>Thermodynamics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Villalba, Miryam I.</creatorcontrib><creatorcontrib>Canul-Tec, Juan C.</creatorcontrib><creatorcontrib>Luna-Martínez, Oscar D.</creatorcontrib><creatorcontrib>Sánchez-Alcalá, Rosalba</creatorcontrib><creatorcontrib>Olamendi-Portugal, Timoteo</creatorcontrib><creatorcontrib>Rudiño-Piñera, Enrique</creatorcontrib><creatorcontrib>Rojas, Sonia</creatorcontrib><creatorcontrib>Sánchez-López, Rosana</creatorcontrib><creatorcontrib>Fernández-Velasco, Daniel A.</creatorcontrib><creatorcontrib>Becerril, Baltazar</creatorcontrib><creatorcontrib>National Autonomous Univ. of Mexico, Mexico City (Mexico)</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>OSTI.GOV - Hybrid</collection><collection>OSTI.GOV</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Villalba, Miryam I.</au><au>Canul-Tec, Juan C.</au><au>Luna-Martínez, Oscar D.</au><au>Sánchez-Alcalá, Rosalba</au><au>Olamendi-Portugal, Timoteo</au><au>Rudiño-Piñera, Enrique</au><au>Rojas, Sonia</au><au>Sánchez-López, Rosana</au><au>Fernández-Velasco, Daniel A.</au><au>Becerril, Baltazar</au><aucorp>National Autonomous Univ. of Mexico, Mexico City (Mexico)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Site-directed Mutagenesis Reveals Regions Implicated in the Stability and Fiber Formation of Human λ3r Light Chains</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2015-01-30</date><risdate>2015</risdate><volume>290</volume><issue>5</issue><spage>2577</spage><epage>2592</epage><pages>2577-2592</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Light chain amyloidosis (AL) is a disease that affects vital organs by the fibrillar aggregation of monoclonal light chains. λ3r germ line is significantly implicated in this disease. In this work, we contrasted the thermodynamic stability and aggregation propensity of 3mJL2 (nonamyloidogenic) and 3rJL2 (amyloidogenic) λ3 germ lines. Because of an inherent limitation (extremely low expression), Cys at position 34 of the 3r germ line was replaced by Tyr reaching a good expression yield. A second substitution (W91A) was introduced in 3r to obtain a better template to incorporate additional mutations. Although the single mutant (C34Y) was not fibrillogenic, the second mutation located at CDR3 (W91A) induced fibrillogenesis. We propose, for the first time, that CDR3 (position 91) affects the stability and fiber formation of human λ3r light chains. Using the double mutant (3rJL2/YA) as template, other variants were constructed to evaluate the importance of those substitutions into the stability and aggregation propensity of λ3 light chains. A change in position 7 (P7D) boosted 3rJL2/YA fibrillogenic properties. Modification of position 48 (I48M) partially reverted 3rJL2/YA fibril aggregation. Finally, changes at positions 8 (P8S) or 40 (P40S) completely reverted fibril formation. These results confirm the influential roles of N-terminal region (positions 7 and 8) and the loop 40–60 (positions 40 and 48) on AL. X-ray crystallography revealed that the three-dimensional topology of the single and double λ3r mutants was not significantly altered. This mutagenic approach helped to identify key regions implicated in λ3 AL.
Background: λ6a and λ3r are the most implicated germ lines in light chain amyloidosis.
Results: Mutagenesis at N-terminal, loop 40–60, and CDR3 regions affected λ3r fibrillogenesis.
Conclusion: Changes at residues 7, 48, and 91 increased fibril formation while changes at residues 8 and 40 reverted fibrillogenesis.
Significance: Characterization of light chain germ lines helps to identify key regions implicated in amyloidosis.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25505244</pmid><doi>10.1074/jbc.M114.629550</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 60 APPLIED LIFE SCIENCES Amino Acid Sequence Amyloid Amyloidosis - metabolism Antibody BASIC BIOLOGICAL SCIENCES Crystallography, X-Ray Fibril Humans Immunoglobulin lambda-Chains - chemistry Immunoglobulin lambda-Chains - metabolism Immunoglobulin Light Chains - chemistry Immunoglobulin Light Chains - metabolism Mutagenesis in Vitro Mutagenesis, Site-Directed - methods Protein Denaturation Protein Structure and Folding Protein Structure, Secondary Protein Structure, Tertiary Thermodynamics |
title | Site-directed Mutagenesis Reveals Regions Implicated in the Stability and Fiber Formation of Human λ3r Light Chains |
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