Structural Basis of Carbohydrate Recognition by the Lectin LecB from Pseudomonas aeruginosa
The crystal structure of Pseudomonas aeruginosa fucose-specific lectin LecB was determined in its metal-bound and metal-free state as well as in complex with fucose, mannose and fructopyranose. All three monosaccharides bind isosterically via direct interactions with two calcium ions as well as dire...
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Veröffentlicht in: | Journal of molecular biology 2003-08, Vol.331 (4), p.861-870 |
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description | The crystal structure of Pseudomonas aeruginosa fucose-specific lectin LecB was determined in its metal-bound and metal-free state as well as in complex with fucose, mannose and fructopyranose. All three monosaccharides bind isosterically via direct interactions with two calcium ions as well as direct hydrogen bonds with several side-chains. The higher affinity for fucose is explained by the details of the binding site around C6 and O1 of fucose. In the mannose and fructose complexes, a carboxylate oxygen atom and one or two hydroxyl groups are partly shielded from solvent upon sugar binding, preventing them from completely fulfilling their hydrogen bonding potential. In the fucose complex, no such defects are observed. Instead, C6 makes favourable interactions with a small hydrophobic patch. Upon demetallization, the C terminus as well as the otherwise rigid metal-binding loop become more mobile and adopt multiple conformations. |
doi_str_mv | 10.1016/S0022-2836(03)00754-X |
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All three monosaccharides bind isosterically via direct interactions with two calcium ions as well as direct hydrogen bonds with several side-chains. The higher affinity for fucose is explained by the details of the binding site around C6 and O1 of fucose. In the mannose and fructose complexes, a carboxylate oxygen atom and one or two hydroxyl groups are partly shielded from solvent upon sugar binding, preventing them from completely fulfilling their hydrogen bonding potential. In the fucose complex, no such defects are observed. Instead, C6 makes favourable interactions with a small hydrophobic patch. Upon demetallization, the C terminus as well as the otherwise rigid metal-binding loop become more mobile and adopt multiple conformations.</description><identifier>ISSN: 0022-2836</identifier><identifier>EISSN: 1089-8638</identifier><identifier>DOI: 10.1016/S0022-2836(03)00754-X</identifier><identifier>PMID: 12909014</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>adhesin ; Binding Sites ; Calcium - metabolism ; carbohydrate ; Carbohydrate Conformation ; Carbohydrate Metabolism ; Carbohydrates - chemistry ; Fructose - analogs & derivatives ; Fructose - chemistry ; Fructose - metabolism ; Fucose - chemistry ; Fucose - metabolism ; Hydrogen Bonding ; lectin ; Lectins - chemistry ; Lectins - metabolism ; Mannose - chemistry ; Mannose - metabolism ; Models, Molecular ; Protein Conformation ; Pseudomonas aeruginosa - chemistry ; Structure-Activity Relationship ; Substrate Specificity</subject><ispartof>Journal of molecular biology, 2003-08, Vol.331 (4), p.861-870</ispartof><rights>2003 Elsevier Science Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c458t-c72569b8c323b2208ba070f6c5f83a475643e843cc60287f2734174ecdcc5863</citedby><cites>FETCH-LOGICAL-c458t-c72569b8c323b2208ba070f6c5f83a475643e843cc60287f2734174ecdcc5863</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0022-2836(03)00754-X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3541,27915,27916,45986</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12909014$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Loris, Remy</creatorcontrib><creatorcontrib>Tielker, Denis</creatorcontrib><creatorcontrib>Jaeger, Karl-Erich</creatorcontrib><creatorcontrib>Wyns, Lode</creatorcontrib><title>Structural Basis of Carbohydrate Recognition by the Lectin LecB from Pseudomonas aeruginosa</title><title>Journal of molecular biology</title><addtitle>J Mol Biol</addtitle><description>The crystal structure of Pseudomonas aeruginosa fucose-specific lectin LecB was determined in its metal-bound and metal-free state as well as in complex with fucose, mannose and fructopyranose. All three monosaccharides bind isosterically via direct interactions with two calcium ions as well as direct hydrogen bonds with several side-chains. The higher affinity for fucose is explained by the details of the binding site around C6 and O1 of fucose. In the mannose and fructose complexes, a carboxylate oxygen atom and one or two hydroxyl groups are partly shielded from solvent upon sugar binding, preventing them from completely fulfilling their hydrogen bonding potential. In the fucose complex, no such defects are observed. Instead, C6 makes favourable interactions with a small hydrophobic patch. Upon demetallization, the C terminus as well as the otherwise rigid metal-binding loop become more mobile and adopt multiple conformations.</description><subject>adhesin</subject><subject>Binding Sites</subject><subject>Calcium - metabolism</subject><subject>carbohydrate</subject><subject>Carbohydrate Conformation</subject><subject>Carbohydrate Metabolism</subject><subject>Carbohydrates - chemistry</subject><subject>Fructose - analogs & derivatives</subject><subject>Fructose - chemistry</subject><subject>Fructose - metabolism</subject><subject>Fucose - chemistry</subject><subject>Fucose - metabolism</subject><subject>Hydrogen Bonding</subject><subject>lectin</subject><subject>Lectins - chemistry</subject><subject>Lectins - metabolism</subject><subject>Mannose - chemistry</subject><subject>Mannose - metabolism</subject><subject>Models, Molecular</subject><subject>Protein Conformation</subject><subject>Pseudomonas aeruginosa - chemistry</subject><subject>Structure-Activity Relationship</subject><subject>Substrate Specificity</subject><issn>0022-2836</issn><issn>1089-8638</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1P3DAURa0KVAban1DkFSqLwPNHbGdVlVGhSCNRdWaB1IXlOC_gahKDnVSaf0-GGdElq7s59129Q8gXBhcMmLpcAnBecCPUVxDnALqUxf0HMmNgqsIoYQ7I7A05Isc5_wWAUkjzkRwxXkEFTM7In-WQRj-Mya3plcsh09jSuUt1fNw0yQ1If6OPD30YQuxpvaHDI9IF-iH027iibYod_ZVxbGIXe5epwzQ-hD5m94kctm6d8fM-T8jq-sdq_rNY3N3czr8vCi9LMxRe81JVtfGCi5pzMLUDDa3yZWuEk7pUUqCRwnsF3OiWayGZlugb78vp0xNytjv7lOLziHmwXcge12vXYxyz1UKxSgj2LsiMUVIrPYHlDvQp5pywtU8pdC5tLAO7tW9f7dutWgvCvtq391PvdD8w1h02_1t73RPwbQfgpONfwGSzD9h7bEKanNomhncmXgCG2pPs</recordid><startdate>20030822</startdate><enddate>20030822</enddate><creator>Loris, Remy</creator><creator>Tielker, Denis</creator><creator>Jaeger, Karl-Erich</creator><creator>Wyns, Lode</creator><general>Elsevier Ltd</general><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>7QL</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>20030822</creationdate><title>Structural Basis of Carbohydrate Recognition by the Lectin LecB from Pseudomonas aeruginosa</title><author>Loris, Remy ; Tielker, Denis ; Jaeger, Karl-Erich ; Wyns, Lode</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c458t-c72569b8c323b2208ba070f6c5f83a475643e843cc60287f2734174ecdcc5863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>adhesin</topic><topic>Binding Sites</topic><topic>Calcium - metabolism</topic><topic>carbohydrate</topic><topic>Carbohydrate Conformation</topic><topic>Carbohydrate Metabolism</topic><topic>Carbohydrates - chemistry</topic><topic>Fructose - analogs & derivatives</topic><topic>Fructose - chemistry</topic><topic>Fructose - metabolism</topic><topic>Fucose - chemistry</topic><topic>Fucose - metabolism</topic><topic>Hydrogen Bonding</topic><topic>lectin</topic><topic>Lectins - chemistry</topic><topic>Lectins - metabolism</topic><topic>Mannose - chemistry</topic><topic>Mannose - metabolism</topic><topic>Models, Molecular</topic><topic>Protein Conformation</topic><topic>Pseudomonas aeruginosa - chemistry</topic><topic>Structure-Activity Relationship</topic><topic>Substrate Specificity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Loris, Remy</creatorcontrib><creatorcontrib>Tielker, Denis</creatorcontrib><creatorcontrib>Jaeger, Karl-Erich</creatorcontrib><creatorcontrib>Wyns, Lode</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Loris, Remy</au><au>Tielker, Denis</au><au>Jaeger, Karl-Erich</au><au>Wyns, Lode</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural Basis of Carbohydrate Recognition by the Lectin LecB from Pseudomonas aeruginosa</atitle><jtitle>Journal of molecular biology</jtitle><addtitle>J Mol Biol</addtitle><date>2003-08-22</date><risdate>2003</risdate><volume>331</volume><issue>4</issue><spage>861</spage><epage>870</epage><pages>861-870</pages><issn>0022-2836</issn><eissn>1089-8638</eissn><abstract>The crystal structure of Pseudomonas aeruginosa fucose-specific lectin LecB was determined in its metal-bound and metal-free state as well as in complex with fucose, mannose and fructopyranose. All three monosaccharides bind isosterically via direct interactions with two calcium ions as well as direct hydrogen bonds with several side-chains. The higher affinity for fucose is explained by the details of the binding site around C6 and O1 of fucose. In the mannose and fructose complexes, a carboxylate oxygen atom and one or two hydroxyl groups are partly shielded from solvent upon sugar binding, preventing them from completely fulfilling their hydrogen bonding potential. In the fucose complex, no such defects are observed. Instead, C6 makes favourable interactions with a small hydrophobic patch. Upon demetallization, the C terminus as well as the otherwise rigid metal-binding loop become more mobile and adopt multiple conformations.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>12909014</pmid><doi>10.1016/S0022-2836(03)00754-X</doi><tpages>10</tpages></addata></record> |
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subjects | adhesin Binding Sites Calcium - metabolism carbohydrate Carbohydrate Conformation Carbohydrate Metabolism Carbohydrates - chemistry Fructose - analogs & derivatives Fructose - chemistry Fructose - metabolism Fucose - chemistry Fucose - metabolism Hydrogen Bonding lectin Lectins - chemistry Lectins - metabolism Mannose - chemistry Mannose - metabolism Models, Molecular Protein Conformation Pseudomonas aeruginosa - chemistry Structure-Activity Relationship Substrate Specificity |
title | Structural Basis of Carbohydrate Recognition by the Lectin LecB from Pseudomonas aeruginosa |
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