"Doubly Selective" Antimicrobial Polymers: How Do They Differentiate between Bacteria?
We have investigated how doubly selective synthetic mimics of antimicrobial peptides (SMAMPs), which can differentiate not only between bacteria and mammalian cells, but also between Gram‐negative and Gram‐positive bacteria, make the latter distinction. By dye‐leakage experiments on model vesicles a...
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Veröffentlicht in: | Chemistry : a European journal 2009-11, Vol.15 (43), p.11710-11714 |
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creator | Lienkamp, Karen Kumar, Kushi-Nidhi Som, Abhigyan Nüsslein, Klaus Tew, Gregory N. |
description | We have investigated how doubly selective synthetic mimics of antimicrobial peptides (SMAMPs), which can differentiate not only between bacteria and mammalian cells, but also between Gram‐negative and Gram‐positive bacteria, make the latter distinction. By dye‐leakage experiments on model vesicles and complementary experiments on bacteria, we were able to relate the Gram selectivity to structural differences of these bacteria types. We showed that the double membrane of E. coli rather than the difference in lipid composition between E. coli and S. aureus was responsible for Gram selectivity. The molecular‐weight‐dependent antimicrobial activity of the SMAMPs was shown to be a sieving effect: while the 3000 g mol−1 SMAMP was able to penetrate the peptidoglycan layer of the Gram‐positive S. aureus bacteria, the 50000 g mol−1 SMAMP got stuck and consequently did not have antimicrobial activity.
Discriminating tastes: “Doubly selective” antimicrobial polymers differentiate not only between bacteria and the cells of the host organism, but also between Gram‐negative and Gram‐positive bacteria. We rationalize this observation by dye‐leakage studies on model vesicles that mimic E. coli and S. aureus, and complementary experiments with bacteria cells. |
doi_str_mv | 10.1002/chem.200802558 |
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Discriminating tastes: “Doubly selective” antimicrobial polymers differentiate not only between bacteria and the cells of the host organism, but also between Gram‐negative and Gram‐positive bacteria. We rationalize this observation by dye‐leakage studies on model vesicles that mimic E. coli and S. aureus, and complementary experiments with bacteria cells.</description><identifier>ISSN: 0947-6539</identifier><identifier>EISSN: 1521-3765</identifier><identifier>DOI: 10.1002/chem.200802558</identifier><identifier>PMID: 19790208</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>Anti-Infective Agents - chemistry ; antibacterial polymers ; Antiinfectives and antibacterials ; Bacteria ; biological activity ; Biomimetic Materials - chemistry ; Dyes ; Escherichia coli ; Escherichia coli - drug effects ; Lipids ; Mammals ; Microbial Sensitivity Tests ; Peptidoglycan - chemistry ; peptidomimetics ; Polymers ; Polymers - chemistry ; ring-opening polymerization ; Selectivity ; Staphylococcus aureus ; Staphylococcus aureus - drug effects ; Vesicles</subject><ispartof>Chemistry : a European journal, 2009-11, Vol.15 (43), p.11710-11714</ispartof><rights>Copyright © 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4468-b85b22a91f11984c3bc0df1a00ea8f9a18695fdd4c4c40c9a1707fccf5f2e9a83</citedby><cites>FETCH-LOGICAL-c4468-b85b22a91f11984c3bc0df1a00ea8f9a18695fdd4c4c40c9a1707fccf5f2e9a83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fchem.200802558$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fchem.200802558$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19790208$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lienkamp, Karen</creatorcontrib><creatorcontrib>Kumar, Kushi-Nidhi</creatorcontrib><creatorcontrib>Som, Abhigyan</creatorcontrib><creatorcontrib>Nüsslein, Klaus</creatorcontrib><creatorcontrib>Tew, Gregory N.</creatorcontrib><title>"Doubly Selective" Antimicrobial Polymers: How Do They Differentiate between Bacteria?</title><title>Chemistry : a European journal</title><addtitle>Chem. Eur. J</addtitle><description>We have investigated how doubly selective synthetic mimics of antimicrobial peptides (SMAMPs), which can differentiate not only between bacteria and mammalian cells, but also between Gram‐negative and Gram‐positive bacteria, make the latter distinction. By dye‐leakage experiments on model vesicles and complementary experiments on bacteria, we were able to relate the Gram selectivity to structural differences of these bacteria types. We showed that the double membrane of E. coli rather than the difference in lipid composition between E. coli and S. aureus was responsible for Gram selectivity. The molecular‐weight‐dependent antimicrobial activity of the SMAMPs was shown to be a sieving effect: while the 3000 g mol−1 SMAMP was able to penetrate the peptidoglycan layer of the Gram‐positive S. aureus bacteria, the 50000 g mol−1 SMAMP got stuck and consequently did not have antimicrobial activity.
Discriminating tastes: “Doubly selective” antimicrobial polymers differentiate not only between bacteria and the cells of the host organism, but also between Gram‐negative and Gram‐positive bacteria. We rationalize this observation by dye‐leakage studies on model vesicles that mimic E. coli and S. aureus, and complementary experiments with bacteria cells.</description><subject>Anti-Infective Agents - chemistry</subject><subject>antibacterial polymers</subject><subject>Antiinfectives and antibacterials</subject><subject>Bacteria</subject><subject>biological activity</subject><subject>Biomimetic Materials - chemistry</subject><subject>Dyes</subject><subject>Escherichia coli</subject><subject>Escherichia coli - drug effects</subject><subject>Lipids</subject><subject>Mammals</subject><subject>Microbial Sensitivity Tests</subject><subject>Peptidoglycan - chemistry</subject><subject>peptidomimetics</subject><subject>Polymers</subject><subject>Polymers - chemistry</subject><subject>ring-opening polymerization</subject><subject>Selectivity</subject><subject>Staphylococcus aureus</subject><subject>Staphylococcus aureus - drug effects</subject><subject>Vesicles</subject><issn>0947-6539</issn><issn>1521-3765</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1vEzEQxS0EomngyhFZPRQuG_yxXttcUEnaBKl8SC3p0fI6Y9Wwm23tTcP-93WVqHAqmpFGGv3eO7yH0BtKJpQQ9sFdQzthhCjChFDP0IgKRgsuK_EcjYguZVEJrg_QYUq_CCG64vwlOqBaasKIGqHl0azb1M2AL6AB14c7OMIn6z60wcWuDrbBP7pmaCGmj3jRbfGsw5fXMOBZ8B4iZNL2gGvotwBr_Nm6HmKwn16hF942CV7v7xj9PDu9nC6K8-_zL9OT88KVZaWKWomaMaupp1Sr0vHakZWnlhCwymtLVaWFX61Kl4e4_JBEeue88Ay0VXyM3u18b2J3u4HUmzYkB01j19BtkpG8pLTkecfo-EmSUVpVOaAMvn8SpFJKrbUoRUYnOzRnlVIEb25iaG0cDCXmoR7zUI95rCcL3u69N3ULq7_4vo8M6B2wDQ0M_7Ez08Xp13_Ni502pB7-PGpt_G0qyaUwV9_mZrmYL_mFuDKK3wO7-KqX</recordid><startdate>20091102</startdate><enddate>20091102</enddate><creator>Lienkamp, Karen</creator><creator>Kumar, Kushi-Nidhi</creator><creator>Som, Abhigyan</creator><creator>Nüsslein, Klaus</creator><creator>Tew, Gregory N.</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</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>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7QL</scope><scope>7T7</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20091102</creationdate><title>"Doubly Selective" Antimicrobial Polymers: How Do They Differentiate between Bacteria?</title><author>Lienkamp, Karen ; Kumar, Kushi-Nidhi ; Som, Abhigyan ; Nüsslein, Klaus ; Tew, Gregory N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4468-b85b22a91f11984c3bc0df1a00ea8f9a18695fdd4c4c40c9a1707fccf5f2e9a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Anti-Infective Agents - chemistry</topic><topic>antibacterial polymers</topic><topic>Antiinfectives and antibacterials</topic><topic>Bacteria</topic><topic>biological activity</topic><topic>Biomimetic Materials - chemistry</topic><topic>Dyes</topic><topic>Escherichia coli</topic><topic>Escherichia coli - drug effects</topic><topic>Lipids</topic><topic>Mammals</topic><topic>Microbial Sensitivity Tests</topic><topic>Peptidoglycan - chemistry</topic><topic>peptidomimetics</topic><topic>Polymers</topic><topic>Polymers - chemistry</topic><topic>ring-opening polymerization</topic><topic>Selectivity</topic><topic>Staphylococcus aureus</topic><topic>Staphylococcus aureus - drug effects</topic><topic>Vesicles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lienkamp, Karen</creatorcontrib><creatorcontrib>Kumar, Kushi-Nidhi</creatorcontrib><creatorcontrib>Som, Abhigyan</creatorcontrib><creatorcontrib>Nüsslein, Klaus</creatorcontrib><creatorcontrib>Tew, Gregory N.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Chemistry : a European journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lienkamp, Karen</au><au>Kumar, Kushi-Nidhi</au><au>Som, Abhigyan</au><au>Nüsslein, Klaus</au><au>Tew, Gregory N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>"Doubly Selective" Antimicrobial Polymers: How Do They Differentiate between Bacteria?</atitle><jtitle>Chemistry : a European journal</jtitle><addtitle>Chem. Eur. J</addtitle><date>2009-11-02</date><risdate>2009</risdate><volume>15</volume><issue>43</issue><spage>11710</spage><epage>11714</epage><pages>11710-11714</pages><issn>0947-6539</issn><eissn>1521-3765</eissn><abstract>We have investigated how doubly selective synthetic mimics of antimicrobial peptides (SMAMPs), which can differentiate not only between bacteria and mammalian cells, but also between Gram‐negative and Gram‐positive bacteria, make the latter distinction. By dye‐leakage experiments on model vesicles and complementary experiments on bacteria, we were able to relate the Gram selectivity to structural differences of these bacteria types. We showed that the double membrane of E. coli rather than the difference in lipid composition between E. coli and S. aureus was responsible for Gram selectivity. The molecular‐weight‐dependent antimicrobial activity of the SMAMPs was shown to be a sieving effect: while the 3000 g mol−1 SMAMP was able to penetrate the peptidoglycan layer of the Gram‐positive S. aureus bacteria, the 50000 g mol−1 SMAMP got stuck and consequently did not have antimicrobial activity.
Discriminating tastes: “Doubly selective” antimicrobial polymers differentiate not only between bacteria and the cells of the host organism, but also between Gram‐negative and Gram‐positive bacteria. We rationalize this observation by dye‐leakage studies on model vesicles that mimic E. coli and S. aureus, and complementary experiments with bacteria cells.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><pmid>19790208</pmid><doi>10.1002/chem.200802558</doi><tpages>5</tpages></addata></record> |
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subjects | Anti-Infective Agents - chemistry antibacterial polymers Antiinfectives and antibacterials Bacteria biological activity Biomimetic Materials - chemistry Dyes Escherichia coli Escherichia coli - drug effects Lipids Mammals Microbial Sensitivity Tests Peptidoglycan - chemistry peptidomimetics Polymers Polymers - chemistry ring-opening polymerization Selectivity Staphylococcus aureus Staphylococcus aureus - drug effects Vesicles |
title | "Doubly Selective" Antimicrobial Polymers: How Do They Differentiate between Bacteria? |
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