Mechanical properties that influence antimicrobial peptide activity in lipid membranes
Antimicrobial peptides are small amphiphilic proteins found in animals and plants as essential components of the innate immune system and whose function is to control bacterial infectious activity. In order to accomplish their function, antimicrobial peptides use different mechanisms of action which...
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Veröffentlicht in: | Applied microbiology and biotechnology 2016-12, Vol.100 (24), p.10251-10263 |
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description | Antimicrobial peptides are small amphiphilic proteins found in animals and plants as essential components of the innate immune system and whose function is to control bacterial infectious activity. In order to accomplish their function, antimicrobial peptides use different mechanisms of action which have been deeply studied in view of their potential exploitation to treat antibiotic-resistant bacterial infections. One of the main mechanisms of action of these peptides is the disruption of the bacterial membrane through pore formation, which, in some cases, takes place via a monomer to oligomer cooperative transition. Previous studies have shown that lipid composition, and the presence of exogenous components, such as cholesterol in model membranes or carotenoids in bacteria, can affect the potency of distinct antimicrobial peptides. At the same time, considering the membrane as a two-dimensional material, it has been shown that membrane composition defines its mechanical properties which might be relevant in many membrane-related processes. Nevertheless, the correlation between the mechanical properties of the membrane and antimicrobial peptide potency has not been considered according to the importance it deserves. The relevance of these mechanical properties in membrane deformation due to peptide insertion is reviewed here for different types of pores in order to elucidate if indeed membrane composition affects antimicrobial peptide activity by modulation of the mechanical properties of the membrane. This would also provide a better understanding of the mechanisms used by bacteria to overcome antimicrobial peptide activity. |
doi_str_mv | 10.1007/s00253-016-7975-9 |
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In order to accomplish their function, antimicrobial peptides use different mechanisms of action which have been deeply studied in view of their potential exploitation to treat antibiotic-resistant bacterial infections. One of the main mechanisms of action of these peptides is the disruption of the bacterial membrane through pore formation, which, in some cases, takes place via a monomer to oligomer cooperative transition. Previous studies have shown that lipid composition, and the presence of exogenous components, such as cholesterol in model membranes or carotenoids in bacteria, can affect the potency of distinct antimicrobial peptides. At the same time, considering the membrane as a two-dimensional material, it has been shown that membrane composition defines its mechanical properties which might be relevant in many membrane-related processes. Nevertheless, the correlation between the mechanical properties of the membrane and antimicrobial peptide potency has not been considered according to the importance it deserves. The relevance of these mechanical properties in membrane deformation due to peptide insertion is reviewed here for different types of pores in order to elucidate if indeed membrane composition affects antimicrobial peptide activity by modulation of the mechanical properties of the membrane. This would also provide a better understanding of the mechanisms used by bacteria to overcome antimicrobial peptide activity.</description><identifier>ISSN: 0175-7598</identifier><identifier>EISSN: 1432-0614</identifier><identifier>DOI: 10.1007/s00253-016-7975-9</identifier><identifier>PMID: 27837316</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Anti-Infective Agents - chemistry ; Anti-Infective Agents - metabolism ; Antibiotic resistance ; Antimicrobial agents ; Antimicrobial Cationic Peptides - chemistry ; Antimicrobial Cationic Peptides - metabolism ; Bacteria ; Bacterial diseases ; Bacterial infections ; Binding sites ; Biomedical and Life Sciences ; Biotechnology ; Carotenoids ; Chemical Phenomena ; Immune system ; Life Sciences ; Lipid Bilayers - chemistry ; Lipid membranes ; Lipids ; Mechanical properties ; Membrane Proteins - metabolism ; Membranes ; Microbial Genetics and Genomics ; Microbiology ; Mini-Review ; Peptides ; Permeability ; Physiological aspects ; Proteins ; Studies</subject><ispartof>Applied microbiology and biotechnology, 2016-12, Vol.100 (24), p.10251-10263</ispartof><rights>Springer-Verlag Berlin Heidelberg 2016</rights><rights>COPYRIGHT 2016 Springer</rights><rights>Applied Microbiology and Biotechnology is a copyright of Springer, 2016.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c543t-e2466e27bd2648c62d3c1fee5c8770c9b3e4000782d93e970292de6422dedb5b3</citedby><cites>FETCH-LOGICAL-c543t-e2466e27bd2648c62d3c1fee5c8770c9b3e4000782d93e970292de6422dedb5b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00253-016-7975-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00253-016-7975-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27837316$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Marín-Medina, Nathaly</creatorcontrib><creatorcontrib>Ramírez, Diego Alejandro</creatorcontrib><creatorcontrib>Trier, Steve</creatorcontrib><creatorcontrib>Leidy, Chad</creatorcontrib><title>Mechanical properties that influence antimicrobial peptide activity in lipid membranes</title><title>Applied microbiology and biotechnology</title><addtitle>Appl Microbiol Biotechnol</addtitle><addtitle>Appl Microbiol Biotechnol</addtitle><description>Antimicrobial peptides are small amphiphilic proteins found in animals and plants as essential components of the innate immune system and whose function is to control bacterial infectious activity. In order to accomplish their function, antimicrobial peptides use different mechanisms of action which have been deeply studied in view of their potential exploitation to treat antibiotic-resistant bacterial infections. One of the main mechanisms of action of these peptides is the disruption of the bacterial membrane through pore formation, which, in some cases, takes place via a monomer to oligomer cooperative transition. Previous studies have shown that lipid composition, and the presence of exogenous components, such as cholesterol in model membranes or carotenoids in bacteria, can affect the potency of distinct antimicrobial peptides. At the same time, considering the membrane as a two-dimensional material, it has been shown that membrane composition defines its mechanical properties which might be relevant in many membrane-related processes. Nevertheless, the correlation between the mechanical properties of the membrane and antimicrobial peptide potency has not been considered according to the importance it deserves. The relevance of these mechanical properties in membrane deformation due to peptide insertion is reviewed here for different types of pores in order to elucidate if indeed membrane composition affects antimicrobial peptide activity by modulation of the mechanical properties of the membrane. This would also provide a better understanding of the mechanisms used by bacteria to overcome antimicrobial peptide activity.</description><subject>Anti-Infective Agents - chemistry</subject><subject>Anti-Infective Agents - metabolism</subject><subject>Antibiotic resistance</subject><subject>Antimicrobial agents</subject><subject>Antimicrobial Cationic Peptides - chemistry</subject><subject>Antimicrobial Cationic Peptides - metabolism</subject><subject>Bacteria</subject><subject>Bacterial diseases</subject><subject>Bacterial infections</subject><subject>Binding sites</subject><subject>Biomedical and Life Sciences</subject><subject>Biotechnology</subject><subject>Carotenoids</subject><subject>Chemical Phenomena</subject><subject>Immune system</subject><subject>Life Sciences</subject><subject>Lipid Bilayers - chemistry</subject><subject>Lipid membranes</subject><subject>Lipids</subject><subject>Mechanical properties</subject><subject>Membrane Proteins - metabolism</subject><subject>Membranes</subject><subject>Microbial Genetics and Genomics</subject><subject>Microbiology</subject><subject>Mini-Review</subject><subject>Peptides</subject><subject>Permeability</subject><subject>Physiological aspects</subject><subject>Proteins</subject><subject>Studies</subject><issn>0175-7598</issn><issn>1432-0614</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkluLFDEQhYMo7jj6A3yRBl_0odfc03lcFi8LK4K315BOV89m6ZtJWtx_bw2zXkYUJJBA5TuHquQQ8pjRU0apeZEp5UrUlOnaWKNqe4dsmBS8pprJu2RDGRaNss0JeZDzNaWMN1rfJyfcNMIIpjfk81sIV36KwQ_VkuYFUomQq3LlSxWnflhhClD5qcQxhjS3cc_BUmKH1VDi11huEKyGuMSuGmFsk58gPyT3ej9keHR7bsmnVy8_nr-pL9-9vjg_u6yDkqLUwKXWwE3bcS2boHknAusBVGiMocG2AiTFSRveWQHWUG55B1py3LtWtWJLnh18sfcvK-TixpgDDAM2Ma_ZsUZRoxsum_9AhWVcKGsQffoHej2vacJBkJJccsGs-kXt_AAOH2suyYe9qTuThnFKBfptyelfKFwd4IvOE_QR60eC50cCZAp8Kzu_5uwuPrw_ZtmBxa_JOUHvlhRHn24co24fEXeIiMOIuH1EnEXNk9vh1naE7qfiRyYQ4Acg49W0g_Tb9P90_Q7HIcM0</recordid><startdate>20161201</startdate><enddate>20161201</enddate><creator>Marín-Medina, Nathaly</creator><creator>Ramírez, Diego Alejandro</creator><creator>Trier, Steve</creator><creator>Leidy, Chad</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><general>Springer Nature B.V</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>ISR</scope><scope>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7WY</scope><scope>7WZ</scope><scope>7X7</scope><scope>7XB</scope><scope>87Z</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FL</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BEZIV</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FRNLG</scope><scope>FYUFA</scope><scope>F~G</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K60</scope><scope>K6~</scope><scope>K9.</scope><scope>L.-</scope><scope>LK8</scope><scope>M0C</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQBIZ</scope><scope>PQBZA</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>7QO</scope></search><sort><creationdate>20161201</creationdate><title>Mechanical properties that influence antimicrobial peptide activity in lipid membranes</title><author>Marín-Medina, Nathaly ; Ramírez, Diego Alejandro ; Trier, Steve ; Leidy, Chad</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c543t-e2466e27bd2648c62d3c1fee5c8770c9b3e4000782d93e970292de6422dedb5b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Anti-Infective Agents - 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Nevertheless, the correlation between the mechanical properties of the membrane and antimicrobial peptide potency has not been considered according to the importance it deserves. The relevance of these mechanical properties in membrane deformation due to peptide insertion is reviewed here for different types of pores in order to elucidate if indeed membrane composition affects antimicrobial peptide activity by modulation of the mechanical properties of the membrane. This would also provide a better understanding of the mechanisms used by bacteria to overcome antimicrobial peptide activity.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>27837316</pmid><doi>10.1007/s00253-016-7975-9</doi><tpages>13</tpages></addata></record> |
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subjects | Anti-Infective Agents - chemistry Anti-Infective Agents - metabolism Antibiotic resistance Antimicrobial agents Antimicrobial Cationic Peptides - chemistry Antimicrobial Cationic Peptides - metabolism Bacteria Bacterial diseases Bacterial infections Binding sites Biomedical and Life Sciences Biotechnology Carotenoids Chemical Phenomena Immune system Life Sciences Lipid Bilayers - chemistry Lipid membranes Lipids Mechanical properties Membrane Proteins - metabolism Membranes Microbial Genetics and Genomics Microbiology Mini-Review Peptides Permeability Physiological aspects Proteins Studies |
title | Mechanical properties that influence antimicrobial peptide activity in lipid membranes |
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