Proteomic analysis of silkworm fat body
Proteomic analysis was performed on the fat body of the fifth instar female silkworm (Bombyx mori, p50) larvae because it is thought that numerous biological substances are synthesized in the fat body. The Drosophila genome and silkworm expression sequence tag (EST) data were applied to the analysis...
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Veröffentlicht in: | Journal of Insect Biotechnology and Sericology 2006, Vol.75(2), pp.47-56 |
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description | Proteomic analysis was performed on the fat body of the fifth instar female silkworm (Bombyx mori, p50) larvae because it is thought that numerous biological substances are synthesized in the fat body. The Drosophila genome and silkworm expression sequence tag (EST) data were applied to the analysis of the fat body proteins and served as the database for protein identification. Protein spots were cut manually from two-dimensional polyacrylamide gel electrophoresis gels, and these spots were treated with 4-vinylpyridine for alkylation. Each spot was analyzed by capillary HPLC coupled with ion-trap mass spectrometry (MS) after proteolysis using modified trypsin. A total of 177 proteins analyzed by MS were identified using the Drosophila genome and silkworm EST data, and these proteins were mapped on 2D-gel. The fat metabolism-related proteins identified in this study were diacylglycerol binding protein, triacylglycerol lipase, and putative hydrolases. Fewer proteins than expected were identified by fat body proteomic analysis. However, nine glycolysis-related proteins were identified in the extracts of the fat bodies. Many cytoskeleton proteins and defense-related proteins were observed in the protein profile. However, some of these proteins were thought to have been derived from the muscles on the epidermis. Calreticulins and chaperonins, including heat-shock proteins, were observed in the fat body extracts. |
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The Drosophila genome and silkworm expression sequence tag (EST) data were applied to the analysis of the fat body proteins and served as the database for protein identification. Protein spots were cut manually from two-dimensional polyacrylamide gel electrophoresis gels, and these spots were treated with 4-vinylpyridine for alkylation. Each spot was analyzed by capillary HPLC coupled with ion-trap mass spectrometry (MS) after proteolysis using modified trypsin. A total of 177 proteins analyzed by MS were identified using the Drosophila genome and silkworm EST data, and these proteins were mapped on 2D-gel. The fat metabolism-related proteins identified in this study were diacylglycerol binding protein, triacylglycerol lipase, and putative hydrolases. Fewer proteins than expected were identified by fat body proteomic analysis. However, nine glycolysis-related proteins were identified in the extracts of the fat bodies. Many cytoskeleton proteins and defense-related proteins were observed in the protein profile. However, some of these proteins were thought to have been derived from the muscles on the epidermis. Calreticulins and chaperonins, including heat-shock proteins, were observed in the fat body extracts.</description><identifier>ISSN: 1346-8073</identifier><identifier>EISSN: 1884-7978</identifier><identifier>DOI: 10.11416/jibs.75.47</identifier><language>eng</language><publisher>Ibaraki: The Japanese Society of Sericultural Science</publisher><subject>BOMBYX MORI ; CORPS GRAS ; ESPECTROMETRIA DE MASAS ; fat body ; FATS ; GENOMAS ; GENOME ; GENOMES ; GRASAS ; MASS SPECTROMETRY ; PROTEINAS ; PROTEINE ; PROTEINS ; proteome ; SPECTROMETRIE DE MASSE ; two-dimensional polyacrylamide gel electrophoresis</subject><ispartof>Journal of Insect Biotechnology and Sericology, 2006, Vol.75(2), pp.47-56</ispartof><rights>2006 by Japan Academic Association for Copyright Clearance (Except in the USA), Copyright Clearance Center, Inc. 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Sericol.</addtitle><description>Proteomic analysis was performed on the fat body of the fifth instar female silkworm (Bombyx mori, p50) larvae because it is thought that numerous biological substances are synthesized in the fat body. The Drosophila genome and silkworm expression sequence tag (EST) data were applied to the analysis of the fat body proteins and served as the database for protein identification. Protein spots were cut manually from two-dimensional polyacrylamide gel electrophoresis gels, and these spots were treated with 4-vinylpyridine for alkylation. Each spot was analyzed by capillary HPLC coupled with ion-trap mass spectrometry (MS) after proteolysis using modified trypsin. A total of 177 proteins analyzed by MS were identified using the Drosophila genome and silkworm EST data, and these proteins were mapped on 2D-gel. The fat metabolism-related proteins identified in this study were diacylglycerol binding protein, triacylglycerol lipase, and putative hydrolases. Fewer proteins than expected were identified by fat body proteomic analysis. However, nine glycolysis-related proteins were identified in the extracts of the fat bodies. Many cytoskeleton proteins and defense-related proteins were observed in the protein profile. However, some of these proteins were thought to have been derived from the muscles on the epidermis. Calreticulins and chaperonins, including heat-shock proteins, were observed in the fat body extracts.</description><subject>BOMBYX MORI</subject><subject>CORPS GRAS</subject><subject>ESPECTROMETRIA DE MASAS</subject><subject>fat body</subject><subject>FATS</subject><subject>GENOMAS</subject><subject>GENOME</subject><subject>GENOMES</subject><subject>GRASAS</subject><subject>MASS SPECTROMETRY</subject><subject>PROTEINAS</subject><subject>PROTEINE</subject><subject>PROTEINS</subject><subject>proteome</subject><subject>SPECTROMETRIE DE MASSE</subject><subject>two-dimensional polyacrylamide gel electrophoresis</subject><issn>1346-8073</issn><issn>1884-7978</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNo9kM1LAzEQxYMoWKsnz8KCB09bk0y-9iRS6hcFe9BzyG6yNeu2qckW6X9vZEUY5j2Yx4_HIHRJ8IwQRsRt5-s0k3zG5BGaEKVYKSupjrMHJkqFJZyis5Q6jAE4ZxN0s4phcGHjm8JsTX9IPhWhLZLvP79D3BStGYo62MM5OmlNn9zFn07R-8Pibf5ULl8fn-f3y7IFyobSWcJBUQFStE6SinFl6ywVthSMIQqLpqqEIxaskA2paa5tMTOO0sYAwBRdj9xdDF97lwbdhX3MzZImjAHHGV7l1N2Y6tJg1k7vot-YeNAmDr7pnf59g5Zc03Ex-X9pPkzUbpsJVyOhNUGbdfRJv6woxjJPFvgBhDZgog</recordid><startdate>200606</startdate><enddate>200606</enddate><creator>Kajiwara, H.(National Inst. of Agrobiological Sciences, Tsukuba, Ibaraki (Japan))</creator><creator>Itou, Y</creator><creator>Imamaki, A</creator><creator>Nakamura, M</creator><creator>Mita, K</creator><creator>Ishizaka, M</creator><general>The Japanese Society of Sericultural Science</general><general>Japan Science and Technology Agency</general><scope>FBQ</scope><scope>7QO</scope><scope>7SS</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>200606</creationdate><title>Proteomic analysis of silkworm fat body</title><author>Kajiwara, H.(National Inst. of Agrobiological Sciences, Tsukuba, Ibaraki (Japan)) ; Itou, Y ; Imamaki, A ; Nakamura, M ; Mita, K ; Ishizaka, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-f324t-ed153826376fe719458db19490d23aa1806c996e1d3d67c1b2141d04ae22ca333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>BOMBYX MORI</topic><topic>CORPS GRAS</topic><topic>ESPECTROMETRIA DE MASAS</topic><topic>fat body</topic><topic>FATS</topic><topic>GENOMAS</topic><topic>GENOME</topic><topic>GENOMES</topic><topic>GRASAS</topic><topic>MASS SPECTROMETRY</topic><topic>PROTEINAS</topic><topic>PROTEINE</topic><topic>PROTEINS</topic><topic>proteome</topic><topic>SPECTROMETRIE DE MASSE</topic><topic>two-dimensional polyacrylamide gel electrophoresis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kajiwara, H.(National Inst. of Agrobiological Sciences, Tsukuba, Ibaraki (Japan))</creatorcontrib><creatorcontrib>Itou, Y</creatorcontrib><creatorcontrib>Imamaki, A</creatorcontrib><creatorcontrib>Nakamura, M</creatorcontrib><creatorcontrib>Mita, K</creatorcontrib><creatorcontrib>Ishizaka, M</creatorcontrib><collection>AGRIS</collection><collection>Biotechnology Research Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of Insect Biotechnology and Sericology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kajiwara, H.(National Inst. of Agrobiological Sciences, Tsukuba, Ibaraki (Japan))</au><au>Itou, Y</au><au>Imamaki, A</au><au>Nakamura, M</au><au>Mita, K</au><au>Ishizaka, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Proteomic analysis of silkworm fat body</atitle><jtitle>Journal of Insect Biotechnology and Sericology</jtitle><addtitle>J. Insect Biotechnol. Sericol.</addtitle><date>2006-06</date><risdate>2006</risdate><volume>75</volume><issue>2</issue><spage>47</spage><epage>56</epage><pages>47-56</pages><issn>1346-8073</issn><eissn>1884-7978</eissn><abstract>Proteomic analysis was performed on the fat body of the fifth instar female silkworm (Bombyx mori, p50) larvae because it is thought that numerous biological substances are synthesized in the fat body. The Drosophila genome and silkworm expression sequence tag (EST) data were applied to the analysis of the fat body proteins and served as the database for protein identification. Protein spots were cut manually from two-dimensional polyacrylamide gel electrophoresis gels, and these spots were treated with 4-vinylpyridine for alkylation. Each spot was analyzed by capillary HPLC coupled with ion-trap mass spectrometry (MS) after proteolysis using modified trypsin. A total of 177 proteins analyzed by MS were identified using the Drosophila genome and silkworm EST data, and these proteins were mapped on 2D-gel. The fat metabolism-related proteins identified in this study were diacylglycerol binding protein, triacylglycerol lipase, and putative hydrolases. Fewer proteins than expected were identified by fat body proteomic analysis. However, nine glycolysis-related proteins were identified in the extracts of the fat bodies. Many cytoskeleton proteins and defense-related proteins were observed in the protein profile. However, some of these proteins were thought to have been derived from the muscles on the epidermis. Calreticulins and chaperonins, including heat-shock proteins, were observed in the fat body extracts.</abstract><cop>Ibaraki</cop><pub>The Japanese Society of Sericultural Science</pub><doi>10.11416/jibs.75.47</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | BOMBYX MORI CORPS GRAS ESPECTROMETRIA DE MASAS fat body FATS GENOMAS GENOME GENOMES GRASAS MASS SPECTROMETRY PROTEINAS PROTEINE PROTEINS proteome SPECTROMETRIE DE MASSE two-dimensional polyacrylamide gel electrophoresis |
title | Proteomic analysis of silkworm fat body |
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