Skin secretion peptides: the molecular facet of the deimatic behavior of the four-eyed frog, Physalaemus nattereri (Anura, Leptodactylidae)
Rationale Amphibians can produce a large amount of bioactive peptides over the skin. In order to map the precise tissue localization of these compounds and evaluate their functions, mass spectrometry imaging (MSI) and gene expression studies were used to investigate a possible correlation between mo...
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Veröffentlicht in: | Rapid communications in mass spectrometry 2015-11, Vol.29 (21), p.2061-2068 |
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creator | Barbosa, Eder Alves Iembo, Tatiane Martins, Graciella Ribeiro Silva, Luciano Paulino Prates, Maura Vianna Andrade, Alan Carvalho Bloch Jr, Carlos |
description | Rationale
Amphibians can produce a large amount of bioactive peptides over the skin. In order to map the precise tissue localization of these compounds and evaluate their functions, mass spectrometry imaging (MSI) and gene expression studies were used to investigate a possible correlation between molecules involved in the antimicrobial defense mechanisms and anti‐predatory behavior by Physalaemus nattereri.
Methods
Total skin secretion of P. nattereri was analyzed by classical Protein Chemistry and proteomic techniques. Intact inguinal macroglands were dissected from the rest of the skin and both tissues were analyzed by MSI and real‐time polymerase chain reaction (RT‐PCR) experiments. Peptides were primarily identified by de novo sequencing, automatic Edman degradation and cDNA data.
Results
Fifteen bradykinin (BK)‐related peptides and two antimicrobial peptides were sequenced and mapped by MSI on the inguinal macrogland and the rest of P. nattereri skin. RT‐PCR results revealed that BK‐related peptide levels of expression were about 30,000 times higher on the inguinal macroglands than on the any other region of the skin, whilst antimicrobial peptide ions appear to be evenly distributed in both investigated regions.
Conclusions
The presence of antimicrobial peptides in all investigated tissue regions is in accordance with the defensive role against microorganisms thoroughly demonstrated in the literature, whereas BK‐related molecules are largely found on the inguinal macroglands suggesting an intriguing link between their noxious activities against potential predators of P. nattereri and the frog's deimatic behavior. Copyright © 2015 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/rcm.7313 |
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Amphibians can produce a large amount of bioactive peptides over the skin. In order to map the precise tissue localization of these compounds and evaluate their functions, mass spectrometry imaging (MSI) and gene expression studies were used to investigate a possible correlation between molecules involved in the antimicrobial defense mechanisms and anti‐predatory behavior by Physalaemus nattereri.
Methods
Total skin secretion of P. nattereri was analyzed by classical Protein Chemistry and proteomic techniques. Intact inguinal macroglands were dissected from the rest of the skin and both tissues were analyzed by MSI and real‐time polymerase chain reaction (RT‐PCR) experiments. Peptides were primarily identified by de novo sequencing, automatic Edman degradation and cDNA data.
Results
Fifteen bradykinin (BK)‐related peptides and two antimicrobial peptides were sequenced and mapped by MSI on the inguinal macrogland and the rest of P. nattereri skin. RT‐PCR results revealed that BK‐related peptide levels of expression were about 30,000 times higher on the inguinal macroglands than on the any other region of the skin, whilst antimicrobial peptide ions appear to be evenly distributed in both investigated regions.
Conclusions
The presence of antimicrobial peptides in all investigated tissue regions is in accordance with the defensive role against microorganisms thoroughly demonstrated in the literature, whereas BK‐related molecules are largely found on the inguinal macroglands suggesting an intriguing link between their noxious activities against potential predators of P. nattereri and the frog's deimatic behavior. Copyright © 2015 John Wiley & Sons, Ltd.</description><identifier>ISSN: 0951-4198</identifier><identifier>EISSN: 1097-0231</identifier><identifier>DOI: 10.1002/rcm.7313</identifier><identifier>PMID: 26443407</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Amino Acid Sequence ; Amphibian Proteins - chemistry ; Amphibian Proteins - genetics ; Amphibian Proteins - metabolism ; Animals ; Antiinfectives and antibacterials ; Antimicrobial Cationic Peptides - chemistry ; Antimicrobial Cationic Peptides - genetics ; Antimicrobial Cationic Peptides - metabolism ; Anura - classification ; Anura - genetics ; Anura - physiology ; Automation ; Behavior, Animal ; Female ; Frogs ; Gene expression ; Male ; Mass Spectrometry ; Molecular Sequence Data ; Peptide Mapping ; Peptides ; Position (location) ; Proteomics ; Rest ; Secretions ; Skin - chemistry ; Skin - metabolism</subject><ispartof>Rapid communications in mass spectrometry, 2015-11, Vol.29 (21), p.2061-2068</ispartof><rights>Copyright © 2015 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4863-724a277eaa8223ec15970e92a1ea852a9ec9f3dc9cb66b4971e5c500d447f2703</citedby><cites>FETCH-LOGICAL-c4863-724a277eaa8223ec15970e92a1ea852a9ec9f3dc9cb66b4971e5c500d447f2703</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%2Frcm.7313$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Frcm.7313$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27922,27923,45572,45573</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26443407$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Barbosa, Eder Alves</creatorcontrib><creatorcontrib>Iembo, Tatiane</creatorcontrib><creatorcontrib>Martins, Graciella Ribeiro</creatorcontrib><creatorcontrib>Silva, Luciano Paulino</creatorcontrib><creatorcontrib>Prates, Maura Vianna</creatorcontrib><creatorcontrib>Andrade, Alan Carvalho</creatorcontrib><creatorcontrib>Bloch Jr, Carlos</creatorcontrib><title>Skin secretion peptides: the molecular facet of the deimatic behavior of the four-eyed frog, Physalaemus nattereri (Anura, Leptodactylidae)</title><title>Rapid communications in mass spectrometry</title><addtitle>Rapid Commun. Mass Spectrom</addtitle><description>Rationale
Amphibians can produce a large amount of bioactive peptides over the skin. In order to map the precise tissue localization of these compounds and evaluate their functions, mass spectrometry imaging (MSI) and gene expression studies were used to investigate a possible correlation between molecules involved in the antimicrobial defense mechanisms and anti‐predatory behavior by Physalaemus nattereri.
Methods
Total skin secretion of P. nattereri was analyzed by classical Protein Chemistry and proteomic techniques. Intact inguinal macroglands were dissected from the rest of the skin and both tissues were analyzed by MSI and real‐time polymerase chain reaction (RT‐PCR) experiments. Peptides were primarily identified by de novo sequencing, automatic Edman degradation and cDNA data.
Results
Fifteen bradykinin (BK)‐related peptides and two antimicrobial peptides were sequenced and mapped by MSI on the inguinal macrogland and the rest of P. nattereri skin. RT‐PCR results revealed that BK‐related peptide levels of expression were about 30,000 times higher on the inguinal macroglands than on the any other region of the skin, whilst antimicrobial peptide ions appear to be evenly distributed in both investigated regions.
Conclusions
The presence of antimicrobial peptides in all investigated tissue regions is in accordance with the defensive role against microorganisms thoroughly demonstrated in the literature, whereas BK‐related molecules are largely found on the inguinal macroglands suggesting an intriguing link between their noxious activities against potential predators of P. nattereri and the frog's deimatic behavior. Copyright © 2015 John Wiley & Sons, Ltd.</description><subject>Amino Acid Sequence</subject><subject>Amphibian Proteins - chemistry</subject><subject>Amphibian Proteins - genetics</subject><subject>Amphibian Proteins - metabolism</subject><subject>Animals</subject><subject>Antiinfectives and antibacterials</subject><subject>Antimicrobial Cationic Peptides - chemistry</subject><subject>Antimicrobial Cationic Peptides - genetics</subject><subject>Antimicrobial Cationic Peptides - metabolism</subject><subject>Anura - classification</subject><subject>Anura - genetics</subject><subject>Anura - physiology</subject><subject>Automation</subject><subject>Behavior, Animal</subject><subject>Female</subject><subject>Frogs</subject><subject>Gene expression</subject><subject>Male</subject><subject>Mass Spectrometry</subject><subject>Molecular Sequence Data</subject><subject>Peptide Mapping</subject><subject>Peptides</subject><subject>Position (location)</subject><subject>Proteomics</subject><subject>Rest</subject><subject>Secretions</subject><subject>Skin - chemistry</subject><subject>Skin - metabolism</subject><issn>0951-4198</issn><issn>1097-0231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0d9qFDEUBvAgil2r4BNIwJsKnZp_M5n0ri7aCusqWhG8CWczZ9y0M5M1yaj7DL60U7utIAheBU5-fCHnI-QxZ0ecMfE8uv5ISy7vkBlnRhdMSH6XzJgpeaG4qffIg5QuGOO8FOw-2ROVUlIxPSM_P1z6gSZ0EbMPA93gJvsG0zHNa6R96NCNHUTagsNMQ_t73KDvIXtHV7iGbz7Em4s2jLHALTa0jeHLIX233iboAPsx0QFyxojR04OTYYxwSBfTW6EBl7edbwCfPST3WugSPtqd--Tjq5fn87Ni8fb09fxkUThVV7LQQoHQGgFqISQ6XhrN0AjgCHUpwKAzrWyccauqWimjOZauZKxRSrdCM7lPDq5zNzF8HTFl2_vksOtgwDAmy3UlmK6Mqf6DCqaUqUs10ad_0YtpG8P0kUlxI5kohf4T6GJIKWJrN3FaZtxazuxVl3bq0l51OdEnu8Bx1WNzC2_Km0BxDb77Drf_DLLv5292gTvvU8Yftx7ipa201KX9tDy1y-XZi8_svLZc_gLicbbG</recordid><startdate>20151115</startdate><enddate>20151115</enddate><creator>Barbosa, Eder Alves</creator><creator>Iembo, Tatiane</creator><creator>Martins, Graciella Ribeiro</creator><creator>Silva, Luciano Paulino</creator><creator>Prates, Maura Vianna</creator><creator>Andrade, Alan Carvalho</creator><creator>Bloch Jr, Carlos</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</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>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>JQ2</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>20151115</creationdate><title>Skin secretion peptides: the molecular facet of the deimatic behavior of the four-eyed frog, Physalaemus nattereri (Anura, Leptodactylidae)</title><author>Barbosa, Eder Alves ; Iembo, Tatiane ; Martins, Graciella Ribeiro ; Silva, Luciano Paulino ; Prates, Maura Vianna ; Andrade, Alan Carvalho ; Bloch Jr, Carlos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4863-724a277eaa8223ec15970e92a1ea852a9ec9f3dc9cb66b4971e5c500d447f2703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Amino Acid Sequence</topic><topic>Amphibian Proteins - chemistry</topic><topic>Amphibian Proteins - genetics</topic><topic>Amphibian Proteins - metabolism</topic><topic>Animals</topic><topic>Antiinfectives and antibacterials</topic><topic>Antimicrobial Cationic Peptides - chemistry</topic><topic>Antimicrobial Cationic Peptides - genetics</topic><topic>Antimicrobial Cationic Peptides - metabolism</topic><topic>Anura - classification</topic><topic>Anura - genetics</topic><topic>Anura - physiology</topic><topic>Automation</topic><topic>Behavior, Animal</topic><topic>Female</topic><topic>Frogs</topic><topic>Gene expression</topic><topic>Male</topic><topic>Mass Spectrometry</topic><topic>Molecular Sequence Data</topic><topic>Peptide Mapping</topic><topic>Peptides</topic><topic>Position (location)</topic><topic>Proteomics</topic><topic>Rest</topic><topic>Secretions</topic><topic>Skin - chemistry</topic><topic>Skin - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Barbosa, Eder Alves</creatorcontrib><creatorcontrib>Iembo, Tatiane</creatorcontrib><creatorcontrib>Martins, Graciella Ribeiro</creatorcontrib><creatorcontrib>Silva, Luciano Paulino</creatorcontrib><creatorcontrib>Prates, Maura Vianna</creatorcontrib><creatorcontrib>Andrade, Alan Carvalho</creatorcontrib><creatorcontrib>Bloch Jr, Carlos</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>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Rapid communications in mass spectrometry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Barbosa, Eder Alves</au><au>Iembo, Tatiane</au><au>Martins, Graciella Ribeiro</au><au>Silva, Luciano Paulino</au><au>Prates, Maura Vianna</au><au>Andrade, Alan Carvalho</au><au>Bloch Jr, Carlos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Skin secretion peptides: the molecular facet of the deimatic behavior of the four-eyed frog, Physalaemus nattereri (Anura, Leptodactylidae)</atitle><jtitle>Rapid communications in mass spectrometry</jtitle><addtitle>Rapid Commun. Mass Spectrom</addtitle><date>2015-11-15</date><risdate>2015</risdate><volume>29</volume><issue>21</issue><spage>2061</spage><epage>2068</epage><pages>2061-2068</pages><issn>0951-4198</issn><eissn>1097-0231</eissn><abstract>Rationale
Amphibians can produce a large amount of bioactive peptides over the skin. In order to map the precise tissue localization of these compounds and evaluate their functions, mass spectrometry imaging (MSI) and gene expression studies were used to investigate a possible correlation between molecules involved in the antimicrobial defense mechanisms and anti‐predatory behavior by Physalaemus nattereri.
Methods
Total skin secretion of P. nattereri was analyzed by classical Protein Chemistry and proteomic techniques. Intact inguinal macroglands were dissected from the rest of the skin and both tissues were analyzed by MSI and real‐time polymerase chain reaction (RT‐PCR) experiments. Peptides were primarily identified by de novo sequencing, automatic Edman degradation and cDNA data.
Results
Fifteen bradykinin (BK)‐related peptides and two antimicrobial peptides were sequenced and mapped by MSI on the inguinal macrogland and the rest of P. nattereri skin. RT‐PCR results revealed that BK‐related peptide levels of expression were about 30,000 times higher on the inguinal macroglands than on the any other region of the skin, whilst antimicrobial peptide ions appear to be evenly distributed in both investigated regions.
Conclusions
The presence of antimicrobial peptides in all investigated tissue regions is in accordance with the defensive role against microorganisms thoroughly demonstrated in the literature, whereas BK‐related molecules are largely found on the inguinal macroglands suggesting an intriguing link between their noxious activities against potential predators of P. nattereri and the frog's deimatic behavior. Copyright © 2015 John Wiley & Sons, Ltd.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>26443407</pmid><doi>10.1002/rcm.7313</doi><tpages>8</tpages></addata></record> |
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subjects | Amino Acid Sequence Amphibian Proteins - chemistry Amphibian Proteins - genetics Amphibian Proteins - metabolism Animals Antiinfectives and antibacterials Antimicrobial Cationic Peptides - chemistry Antimicrobial Cationic Peptides - genetics Antimicrobial Cationic Peptides - metabolism Anura - classification Anura - genetics Anura - physiology Automation Behavior, Animal Female Frogs Gene expression Male Mass Spectrometry Molecular Sequence Data Peptide Mapping Peptides Position (location) Proteomics Rest Secretions Skin - chemistry Skin - metabolism |
title | Skin secretion peptides: the molecular facet of the deimatic behavior of the four-eyed frog, Physalaemus nattereri (Anura, Leptodactylidae) |
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