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Direct profiling of the phospholipid composition of adult Caenorhabditis elegans using whole-body imaging mass spectrometry
A protocol for the direct analysis of the phospholipid composition in the whole body of adult soil nematode, Caenorhabditis elegans (C. elegans), was developed, which combined freeze-cracking of the exoskeletal cuticle and matrix-assisted laser desorption/ionization-imaging mass spectrometry (MALDI-...
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Published in: | Analytical and bioanalytical chemistry 2015, Vol.407 (25), p.7589-7602 |
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creator | Hameed, Saira Ikegami, Koji Sugiyama, Eiji Matsushita, Shoko Kimura, Yoshishige Hayasaka, Takahiro Sugiura, Yuki Masaki, Noritaka Waki, Michihiko Ohta, Isao Hossen, Md Amir Setou, Mitsutoshi |
description | A protocol for the direct analysis of the phospholipid composition in the whole body of adult soil nematode, Caenorhabditis elegans (C. elegans), was developed, which combined freeze-cracking of the exoskeletal cuticle and matrix-assisted laser desorption/ionization-imaging mass spectrometry (MALDI-IMS). Biomolecules in the m/z range from 700 to 900 were more effectively detected in the freeze-cracked than from simple frozen adult nematode bodies. Different distribution of biomolecules was observed in a nematode body when the matrix was applied with a sublimation deposition method. The whole-body IMS technique was applied on genetically deficient mutant C. elegans to combine whole-body lipidomics and genetics, by comparing the fatty acid compositions, especially of the phosphatidylcholine (PC) species, between the wild-type and fat-1 mutants, which lack the gene encoding an n-3 fatty acid desaturase. A significant reduction of PC(20:5/20:5) and PC(20:4/20:5) and a marked increase of PC(20:4/20:4), PC(20:3/20:4), and PC(20:3/20:3) were detected in the fat-1 mutants in positive ion mode. In addition, phospholipid compositions other than PCs were analyzed in negative ion mode. A loss of a possible phosphatidylinositol (PI) with 18:0/20:5 and a compensative accumulation of putative PI(18:0/20:4) were detected in the fat-1 mutants. In conclusion, the whole-body MALDI-IMS technique is useful for the profiling of multiple biomolecules in C. elegans in both intra- and inter-individual levels. |
doi_str_mv | 10.1007/s00216-015-8932-7 |
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Biomolecules in the m/z range from 700 to 900 were more effectively detected in the freeze-cracked than from simple frozen adult nematode bodies. Different distribution of biomolecules was observed in a nematode body when the matrix was applied with a sublimation deposition method. The whole-body IMS technique was applied on genetically deficient mutant C. elegans to combine whole-body lipidomics and genetics, by comparing the fatty acid compositions, especially of the phosphatidylcholine (PC) species, between the wild-type and fat-1 mutants, which lack the gene encoding an n-3 fatty acid desaturase. A significant reduction of PC(20:5/20:5) and PC(20:4/20:5) and a marked increase of PC(20:4/20:4), PC(20:3/20:4), and PC(20:3/20:3) were detected in the fat-1 mutants in positive ion mode. In addition, phospholipid compositions other than PCs were analyzed in negative ion mode. A loss of a possible phosphatidylinositol (PI) with 18:0/20:5 and a compensative accumulation of putative PI(18:0/20:4) were detected in the fat-1 mutants. In conclusion, the whole-body MALDI-IMS technique is useful for the profiling of multiple biomolecules in C. elegans in both intra- and inter-individual levels.</description><identifier>ISSN: 1618-2642</identifier><identifier>EISSN: 1618-2650</identifier><identifier>DOI: 10.1007/s00216-015-8932-7</identifier><identifier>PMID: 26310845</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adults ; Analytical Chemistry ; Animals ; Biochemistry ; Biomolecules ; Caenorhabditis elegans ; Caenorhabditis elegans - chemistry ; Caenorhabditis elegans - genetics ; Caenorhabditis elegans - ultrastructure ; Characterization and Evaluation of Materials ; Chemical properties ; Chemistry ; Chemistry and Materials Science ; Encoding ; fatty acid composition ; Fatty acids ; Fatty Acids - analysis ; Fatty Acids - genetics ; Food Science ; Freezing ; genes ; Genetics ; Identification and classification ; image analysis ; Ionization ; Laboratory Medicine ; Lasers ; Mass spectrometry ; Methods ; Monitoring/Environmental Analysis ; mutants ; Mycotoxins ; Nematodes ; New Applications of Mass Spectrometry in Biomedicine ; omega-3 fatty acids ; Peptides ; phosphatidylcholines ; Phospholipids ; Phospholipids - analysis ; Phospholipids - genetics ; Physiological aspects ; Profiling ; Research Paper ; Scientific imaging ; soil nematodes ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods ; Stable isotopes ; stearoyl-CoA desaturase ; Sublimation ; Whole Body Imaging - methods</subject><ispartof>Analytical and bioanalytical chemistry, 2015, Vol.407 (25), p.7589-7602</ispartof><rights>The Author(s) 2015</rights><rights>COPYRIGHT 2015 Springer</rights><rights>Springer-Verlag Berlin Heidelberg 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c856t-dc4ae85c14dc2e304fa5f99ae9db3873564c5df6db4886101b11de53661a20fb3</citedby><cites>FETCH-LOGICAL-c856t-dc4ae85c14dc2e304fa5f99ae9db3873564c5df6db4886101b11de53661a20fb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26310845$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hameed, Saira</creatorcontrib><creatorcontrib>Ikegami, Koji</creatorcontrib><creatorcontrib>Sugiyama, Eiji</creatorcontrib><creatorcontrib>Matsushita, Shoko</creatorcontrib><creatorcontrib>Kimura, Yoshishige</creatorcontrib><creatorcontrib>Hayasaka, Takahiro</creatorcontrib><creatorcontrib>Sugiura, Yuki</creatorcontrib><creatorcontrib>Masaki, Noritaka</creatorcontrib><creatorcontrib>Waki, Michihiko</creatorcontrib><creatorcontrib>Ohta, Isao</creatorcontrib><creatorcontrib>Hossen, Md Amir</creatorcontrib><creatorcontrib>Setou, Mitsutoshi</creatorcontrib><title>Direct profiling of the phospholipid composition of adult Caenorhabditis elegans using whole-body imaging mass spectrometry</title><title>Analytical and bioanalytical chemistry</title><addtitle>Anal Bioanal Chem</addtitle><addtitle>Anal Bioanal Chem</addtitle><description>A protocol for the direct analysis of the phospholipid composition in the whole body of adult soil nematode, Caenorhabditis elegans (C. elegans), was developed, which combined freeze-cracking of the exoskeletal cuticle and matrix-assisted laser desorption/ionization-imaging mass spectrometry (MALDI-IMS). Biomolecules in the m/z range from 700 to 900 were more effectively detected in the freeze-cracked than from simple frozen adult nematode bodies. Different distribution of biomolecules was observed in a nematode body when the matrix was applied with a sublimation deposition method. The whole-body IMS technique was applied on genetically deficient mutant C. elegans to combine whole-body lipidomics and genetics, by comparing the fatty acid compositions, especially of the phosphatidylcholine (PC) species, between the wild-type and fat-1 mutants, which lack the gene encoding an n-3 fatty acid desaturase. A significant reduction of PC(20:5/20:5) and PC(20:4/20:5) and a marked increase of PC(20:4/20:4), PC(20:3/20:4), and PC(20:3/20:3) were detected in the fat-1 mutants in positive ion mode. In addition, phospholipid compositions other than PCs were analyzed in negative ion mode. A loss of a possible phosphatidylinositol (PI) with 18:0/20:5 and a compensative accumulation of putative PI(18:0/20:4) were detected in the fat-1 mutants. In conclusion, the whole-body MALDI-IMS technique is useful for the profiling of multiple biomolecules in C. elegans in both intra- and inter-individual levels.</description><subject>Adults</subject><subject>Analytical Chemistry</subject><subject>Animals</subject><subject>Biochemistry</subject><subject>Biomolecules</subject><subject>Caenorhabditis elegans</subject><subject>Caenorhabditis elegans - chemistry</subject><subject>Caenorhabditis elegans - genetics</subject><subject>Caenorhabditis elegans - ultrastructure</subject><subject>Characterization and Evaluation of Materials</subject><subject>Chemical properties</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Encoding</subject><subject>fatty acid composition</subject><subject>Fatty acids</subject><subject>Fatty Acids - analysis</subject><subject>Fatty Acids - genetics</subject><subject>Food Science</subject><subject>Freezing</subject><subject>genes</subject><subject>Genetics</subject><subject>Identification and classification</subject><subject>image analysis</subject><subject>Ionization</subject><subject>Laboratory Medicine</subject><subject>Lasers</subject><subject>Mass spectrometry</subject><subject>Methods</subject><subject>Monitoring/Environmental Analysis</subject><subject>mutants</subject><subject>Mycotoxins</subject><subject>Nematodes</subject><subject>New Applications of Mass Spectrometry in Biomedicine</subject><subject>omega-3 fatty acids</subject><subject>Peptides</subject><subject>phosphatidylcholines</subject><subject>Phospholipids</subject><subject>Phospholipids - analysis</subject><subject>Phospholipids - genetics</subject><subject>Physiological aspects</subject><subject>Profiling</subject><subject>Research Paper</subject><subject>Scientific imaging</subject><subject>soil nematodes</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods</subject><subject>Stable isotopes</subject><subject>stearoyl-CoA desaturase</subject><subject>Sublimation</subject><subject>Whole Body Imaging - methods</subject><issn>1618-2642</issn><issn>1618-2650</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqNkk2L1TAUhosozjj6A9xowY2bjvluuhGG6ycMuNBZhzQ57c3QJjVpRy7-eVM7XkYXMoSQkPOcNycnb1E8x-gcI1S_SQgRLCqEeSUbSqr6QXGKBZYVERw9PO4ZOSmepHSNMiixeFycEEExkoyfFj_fuQhmLqcYOjc435ehK-c9lNM-pDwHNzlbmjBOIbnZBb_GtV2Gudxp8CHudWtzIJUwQK99Kpe0qvzIqVC1wR5KN-p-PRp1SmWa8m0xjDDHw9PiUaeHBM9u17Pi6sP7b7tP1eWXj593F5eVkVzMlTVMg-QGM2sIUMQ6zbum0dDYlsqacsEMt52wLZNSYIRbjC1wKgTWBHUtPSvebrrT0o5gDfg56kFNMVcWDypop_6OeLdXfbhRjNecSpYFXt8KxPB9gTSr0SUDw6A9hCUpnDHOCCXyHigTUhJci3ugmDaskbzO6Kt_0OuwRJ-b9puq1z-mmTrfqF4PoJzvQn6NycPC6EzwkH8Y1AUjDUaiQWsFeEswMaQUoTv2BCO1OkxtDlPZOGp1mFpLeXG3mceMP5bKANmAlEO-h3in1v-ovtySOh2U7qNL6uorQVigjDZCIvoLEgfm2g</recordid><startdate>2015</startdate><enddate>2015</enddate><creator>Hameed, Saira</creator><creator>Ikegami, Koji</creator><creator>Sugiyama, Eiji</creator><creator>Matsushita, Shoko</creator><creator>Kimura, Yoshishige</creator><creator>Hayasaka, Takahiro</creator><creator>Sugiura, Yuki</creator><creator>Masaki, Noritaka</creator><creator>Waki, Michihiko</creator><creator>Ohta, Isao</creator><creator>Hossen, Md Amir</creator><creator>Setou, Mitsutoshi</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><general>Springer Nature B.V</general><scope>FBQ</scope><scope>C6C</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>3V.</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8BQ</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>F28</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H8D</scope><scope>H8G</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>JQ2</scope><scope>K9.</scope><scope>KB.</scope><scope>KR7</scope><scope>L7M</scope><scope>LK8</scope><scope>L~C</scope><scope>L~D</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>7QH</scope><scope>7UA</scope><scope>5PM</scope></search><sort><creationdate>2015</creationdate><title>Direct profiling of the phospholipid composition of adult Caenorhabditis elegans using whole-body imaging mass spectrometry</title><author>Hameed, Saira ; Ikegami, Koji ; Sugiyama, Eiji ; Matsushita, Shoko ; Kimura, Yoshishige ; Hayasaka, Takahiro ; Sugiura, Yuki ; Masaki, Noritaka ; Waki, Michihiko ; Ohta, Isao ; Hossen, Md Amir ; Setou, Mitsutoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c856t-dc4ae85c14dc2e304fa5f99ae9db3873564c5df6db4886101b11de53661a20fb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adults</topic><topic>Analytical Chemistry</topic><topic>Animals</topic><topic>Biochemistry</topic><topic>Biomolecules</topic><topic>Caenorhabditis elegans</topic><topic>Caenorhabditis elegans - chemistry</topic><topic>Caenorhabditis elegans - genetics</topic><topic>Caenorhabditis elegans - ultrastructure</topic><topic>Characterization and Evaluation of Materials</topic><topic>Chemical properties</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Encoding</topic><topic>fatty acid composition</topic><topic>Fatty acids</topic><topic>Fatty Acids - analysis</topic><topic>Fatty Acids - genetics</topic><topic>Food Science</topic><topic>Freezing</topic><topic>genes</topic><topic>Genetics</topic><topic>Identification and classification</topic><topic>image analysis</topic><topic>Ionization</topic><topic>Laboratory Medicine</topic><topic>Lasers</topic><topic>Mass spectrometry</topic><topic>Methods</topic><topic>Monitoring/Environmental Analysis</topic><topic>mutants</topic><topic>Mycotoxins</topic><topic>Nematodes</topic><topic>New Applications of Mass Spectrometry in Biomedicine</topic><topic>omega-3 fatty acids</topic><topic>Peptides</topic><topic>phosphatidylcholines</topic><topic>Phospholipids</topic><topic>Phospholipids - 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Biomolecules in the m/z range from 700 to 900 were more effectively detected in the freeze-cracked than from simple frozen adult nematode bodies. Different distribution of biomolecules was observed in a nematode body when the matrix was applied with a sublimation deposition method. The whole-body IMS technique was applied on genetically deficient mutant C. elegans to combine whole-body lipidomics and genetics, by comparing the fatty acid compositions, especially of the phosphatidylcholine (PC) species, between the wild-type and fat-1 mutants, which lack the gene encoding an n-3 fatty acid desaturase. A significant reduction of PC(20:5/20:5) and PC(20:4/20:5) and a marked increase of PC(20:4/20:4), PC(20:3/20:4), and PC(20:3/20:3) were detected in the fat-1 mutants in positive ion mode. In addition, phospholipid compositions other than PCs were analyzed in negative ion mode. A loss of a possible phosphatidylinositol (PI) with 18:0/20:5 and a compensative accumulation of putative PI(18:0/20:4) were detected in the fat-1 mutants. In conclusion, the whole-body MALDI-IMS technique is useful for the profiling of multiple biomolecules in C. elegans in both intra- and inter-individual levels.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>26310845</pmid><doi>10.1007/s00216-015-8932-7</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adults Analytical Chemistry Animals Biochemistry Biomolecules Caenorhabditis elegans Caenorhabditis elegans - chemistry Caenorhabditis elegans - genetics Caenorhabditis elegans - ultrastructure Characterization and Evaluation of Materials Chemical properties Chemistry Chemistry and Materials Science Encoding fatty acid composition Fatty acids Fatty Acids - analysis Fatty Acids - genetics Food Science Freezing genes Genetics Identification and classification image analysis Ionization Laboratory Medicine Lasers Mass spectrometry Methods Monitoring/Environmental Analysis mutants Mycotoxins Nematodes New Applications of Mass Spectrometry in Biomedicine omega-3 fatty acids Peptides phosphatidylcholines Phospholipids Phospholipids - analysis Phospholipids - genetics Physiological aspects Profiling Research Paper Scientific imaging soil nematodes Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods Stable isotopes stearoyl-CoA desaturase Sublimation Whole Body Imaging - methods |
title | Direct profiling of the phospholipid composition of adult Caenorhabditis elegans using whole-body imaging mass spectrometry |
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