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rivas.xml

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<Publisher>
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		<PublisherName>University of South Bohemia, Ceske Budejovice and Versita, Warsaw</PublisherName>
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	<Journal>
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			<JournalPrintISSN>1214-021X</JournalPrintISSN>
			<JournalElectronicISSN>1214-0287</JournalElectronicISSN>
			<JournalTitle>Journal of Applied Biomedicine</JournalTitle>
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		<Volume>
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				<VolumeNumber>8</VolumeNumber>
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			<Issue>
				<IssueInfo IssueType="Regular">
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						<CoverDate Year="2010" Month="9" Day="1"/>
						<CoverDisplay>Number 3 / September 2010</CoverDisplay>
					</IssuePublicationDate>
					<IssueID>W7U4305X5R35</IssueID>
					<IssueURL>http://versita.metapress.com/link.asp?target=issue&amp;id=W7U4305X5R35</IssueURL>
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				<Article ArticleType="Original">
					<ArticleInfo Free="No" ESM="No">
						<ArticleDOI>10.2478/v10136-009-0019-3</ArticleDOI>
						<ArticlePII>612887H7X1W59254</ArticlePII>
						<ArticleSequenceNumber>5</ArticleSequenceNumber>
						<ArticleTitle Language="En">Membrane-active peptides as anti-infectious agents</ArticleTitle>
						<ArticleFirstPage>159</ArticleFirstPage>
						<ArticleLastPage>167</ArticleLastPage>
						<ArticleHistory>
							<RegistrationDate>20100708</RegistrationDate>
							<ReceivedDate>20100708</ReceivedDate>
							<Accepted>20100708</Accepted>
							<OnlineDate>20100708</OnlineDate>
						</ArticleHistory>
						<FullTextFileName>612887H7X1W59254.pdf</FullTextFileName>
						<FullTextURL>http://versita.metapress.com/link.asp?target=contribution&amp;id=612887H7X1W59254</FullTextURL>
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					<ArticleHeader>
						<AuthorGroup>
							<Author AffiliationID="A1">
								<GivenName>Luis</GivenName>
								<Initials/>
								<FamilyName>Rivas</FamilyName>
								<Degrees/>
								<Roles/>
							</Author>
							<Author AffiliationID="A1">
								<GivenName>Juan</GivenName>
								<Initials>Román</Initials>
								<FamilyName>Luque-Ortega</FamilyName>
								<Degrees/>
								<Roles/>
							</Author>
							<Author AffiliationID="A1">
								<GivenName>María</GivenName>
								<Initials/>
								<FamilyName>Fernández-Reyes</FamilyName>
								<Degrees/>
								<Roles/>
							</Author>
							<Author AffiliationID="A2">
								<GivenName>David</GivenName>
								<Initials/>
								<FamilyName>Andreu</FamilyName>
								<Degrees/>
								<Roles/>
							</Author>
							<Affiliation AFFID="A1">
								<OrgDivision/>
								<OrgName>Department of Physico Chemical Biology CSIC, Centro de Investigaciones Biológicas — CSIC, Madrid, Spain</OrgName>
								<OrgAddress/>
							</Affiliation>
							<Affiliation AFFID="A2">
								<OrgDivision/>
								<OrgName>Department of Experimental and Health Sciences, Barcelona Biomedical Research Park, Universitat Pompeu Fabra, Barcelona, Spain</OrgName>
								<OrgAddress/>
							</Affiliation>
						</AuthorGroup>
						<Abstract Language="En">The lipid components of pathogen cell membranes have been considered as a poor pharmacological target, due to their universal distribution and apparent homogeneity throughout living organisms. Among the rare exceptions to this view one could mention polyene antibiotics such as amphotericin, or peptide antibiotics such as the polymyxins and the gramicidins. In the last two decades, however, the above notion has been challenged by two main lines of discovery; first, natural antimicrobial peptides (AMPs) that kill pathogens by interaction with phospholipids and membrane permeabilization, and secondly, cell-penetrating peptides (CPPs), capable of introducing into cells a variety of cargoes in the absence of specific receptors, again by interaction at some point with membrane phospholipids. For both AMPs and CPPs, the pharmacological proof-of-concept has been successfully demonstrated, and promising applications as nanobiotechnological tools have been envisaged though not hitherto materialized in clinical settings. In this review we briefly examine the pros and cons of these two classes of therapeutic agents, as well as strategies aimed at rationalizing and expanding their potentiality.</Abstract>
						<KeywordGroup Language="En">
							<Keyword>membrane</Keyword>
						</KeywordGroup>
						<KeywordGroup Language="En">
							<Keyword>cell-penetrating peptide</Keyword>
						</KeywordGroup>
						<KeywordGroup Language="En">
							<Keyword>antimicrobial peptide</Keyword>
						</KeywordGroup>
						<KeywordGroup Language="En">
							<Keyword>antibiotic resistance</Keyword>
						</KeywordGroup>
						<KeywordGroup Language="En">
							<Keyword>infectious disease</Keyword>
						</KeywordGroup>
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