Identification of transglutaminase 2 kinase substrates using a novel on-chip activity assay
Transglutaminase 2 (TG2) is an enzyme that plays a critical role in a wide variety of cellular processes through its multifunctional activities. TG2 kinase has emerged as an important regulator of apoptosis, as well as of chromatin structure and function. However, systematic investigation of TG2 kin...
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Veröffentlicht in: | Biosensors & bioelectronics 2016-08, Vol.82, p.40-48 |
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creator | Jung, Se-Hui Kong, Deok-Hoon Jeon, Hye-Yoon Ji, Su-Hyun Han, Eun-Taek Park, Won Sun Hong, Seok-Ho Kim, Min-Soo Kim, Young-Myeong Ha, Kwon-Soo |
description | Transglutaminase 2 (TG2) is an enzyme that plays a critical role in a wide variety of cellular processes through its multifunctional activities. TG2 kinase has emerged as an important regulator of apoptosis, as well as of chromatin structure and function. However, systematic investigation of TG2 kinase substrates is limited due to a lack of a suitable TG2 kinase activity assays. Thus, we developed a novel on-chip TG2 kinase activity assay for quantitative determination of TG2 kinase activity and for screening TG2 kinase substrate proteins in a high-throughput manner. Quantitative TG2 kinase activity was determined by selective detection of substrate protein phosphorylation on the surface of well-type amine arrays. The limit of detection (LOD) of this assay was 4.34μg/ml. We successfully applied this new activity assay to the kinetic analysis of 27 TG2-related proteins for TG2 kinase activity in a high-throughput manner and determined Michaelis-Menten constants (Km) of these proteins. We used the Km values and cellular locations of the TG2-related proteins to construct a substrate affinity map for TG2 kinase. Therefore, this on-chip TG2 kinase activity assay has a strong potential for the systematic investigation of substrate proteins and will be helpful for studying new physiological functions.
•We developed a new on-chip TG2 kinase activity assay.•We successfully applied this activity assay to the kinetic analysis of 27 TG2-related proteins for TG2 kinase activity.•We used the Km values obtained from the large-scale analyses to construct a substrate affinity map for TG2 kinase.•Thus, this on-chip TG2 kinase activity assay has a strong potential for the systematic investigation of substrate proteins.•And will be helpful for studying its new physiological functions. |
doi_str_mv | 10.1016/j.bios.2016.03.064 |
format | Article |
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•We developed a new on-chip TG2 kinase activity assay.•We successfully applied this activity assay to the kinetic analysis of 27 TG2-related proteins for TG2 kinase activity.•We used the Km values obtained from the large-scale analyses to construct a substrate affinity map for TG2 kinase.•Thus, this on-chip TG2 kinase activity assay has a strong potential for the systematic investigation of substrate proteins.•And will be helpful for studying its new physiological functions.</description><identifier>ISSN: 0956-5663</identifier><identifier>EISSN: 1873-4235</identifier><identifier>DOI: 10.1016/j.bios.2016.03.064</identifier><identifier>PMID: 27040940</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>Apoptosis ; Arrays ; Assaying ; Biosensing Techniques - instrumentation ; Cellular ; Constants ; Enzyme Assays - instrumentation ; Enzymes ; Equipment Design ; GTP-Binding Proteins - metabolism ; Humans ; Kinases ; Kinetics ; Michaelis-Menten constants (Km) ; On-chip TG2 kinase activity assay ; Phosphorylation ; Protein Array Analysis - instrumentation ; Protein Kinases - metabolism ; Proteins ; Substrate affinity map ; Substrate Specificity ; Substrates ; Transglutaminase 2 ; Transglutaminases - metabolism</subject><ispartof>Biosensors & bioelectronics, 2016-08, Vol.82, p.40-48</ispartof><rights>2016 Elsevier B.V.</rights><rights>Copyright © 2016 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c459t-3269c35b72453c022201c06195999892fcdfd2df74d24903b6ea547754dfc72a3</citedby><cites>FETCH-LOGICAL-c459t-3269c35b72453c022201c06195999892fcdfd2df74d24903b6ea547754dfc72a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.bios.2016.03.064$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27040940$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jung, Se-Hui</creatorcontrib><creatorcontrib>Kong, Deok-Hoon</creatorcontrib><creatorcontrib>Jeon, Hye-Yoon</creatorcontrib><creatorcontrib>Ji, Su-Hyun</creatorcontrib><creatorcontrib>Han, Eun-Taek</creatorcontrib><creatorcontrib>Park, Won Sun</creatorcontrib><creatorcontrib>Hong, Seok-Ho</creatorcontrib><creatorcontrib>Kim, Min-Soo</creatorcontrib><creatorcontrib>Kim, Young-Myeong</creatorcontrib><creatorcontrib>Ha, Kwon-Soo</creatorcontrib><title>Identification of transglutaminase 2 kinase substrates using a novel on-chip activity assay</title><title>Biosensors & bioelectronics</title><addtitle>Biosens Bioelectron</addtitle><description>Transglutaminase 2 (TG2) is an enzyme that plays a critical role in a wide variety of cellular processes through its multifunctional activities. TG2 kinase has emerged as an important regulator of apoptosis, as well as of chromatin structure and function. However, systematic investigation of TG2 kinase substrates is limited due to a lack of a suitable TG2 kinase activity assays. Thus, we developed a novel on-chip TG2 kinase activity assay for quantitative determination of TG2 kinase activity and for screening TG2 kinase substrate proteins in a high-throughput manner. Quantitative TG2 kinase activity was determined by selective detection of substrate protein phosphorylation on the surface of well-type amine arrays. The limit of detection (LOD) of this assay was 4.34μg/ml. We successfully applied this new activity assay to the kinetic analysis of 27 TG2-related proteins for TG2 kinase activity in a high-throughput manner and determined Michaelis-Menten constants (Km) of these proteins. We used the Km values and cellular locations of the TG2-related proteins to construct a substrate affinity map for TG2 kinase. Therefore, this on-chip TG2 kinase activity assay has a strong potential for the systematic investigation of substrate proteins and will be helpful for studying new physiological functions.
•We developed a new on-chip TG2 kinase activity assay.•We successfully applied this activity assay to the kinetic analysis of 27 TG2-related proteins for TG2 kinase activity.•We used the Km values obtained from the large-scale analyses to construct a substrate affinity map for TG2 kinase.•Thus, this on-chip TG2 kinase activity assay has a strong potential for the systematic investigation of substrate proteins.•And will be helpful for studying its new physiological functions.</description><subject>Apoptosis</subject><subject>Arrays</subject><subject>Assaying</subject><subject>Biosensing Techniques - instrumentation</subject><subject>Cellular</subject><subject>Constants</subject><subject>Enzyme Assays - instrumentation</subject><subject>Enzymes</subject><subject>Equipment Design</subject><subject>GTP-Binding Proteins - metabolism</subject><subject>Humans</subject><subject>Kinases</subject><subject>Kinetics</subject><subject>Michaelis-Menten constants (Km)</subject><subject>On-chip TG2 kinase activity assay</subject><subject>Phosphorylation</subject><subject>Protein Array Analysis - instrumentation</subject><subject>Protein Kinases - metabolism</subject><subject>Proteins</subject><subject>Substrate affinity map</subject><subject>Substrate Specificity</subject><subject>Substrates</subject><subject>Transglutaminase 2</subject><subject>Transglutaminases - metabolism</subject><issn>0956-5663</issn><issn>1873-4235</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc2KFDEUhYMoTk_rC7iQLN1UefNfATcy-DMw4EZXLkIqSY1pq5O2kmrotzdNjy5nVrmQ7x6S8yH0hkBPgMj3u36MufS0zT2wHiR_hjZkUKzjlInnaANayE5Iya7QdSk7AFBEw0t0RRVw0Bw26OetD6nGKTpbY044T7guNpX7ea12H5MtAVP8-zKUdSzttoaC1xLTPbY45WOYcU6d-xUP2Loaj7GesC3Fnl6hF5OdS3j9cG7Rj8-fvt987e6-fbm9-XjXOS507RiV2jExKsoFc0Bp-5ADSbTQWg-aTs5PnvpJcU-5BjbKYAVXSnA_OUUt26J3l9zDkv-soVSzj8WFebYp5LUYMhAJmg6aPI0q3XoRshX4NDoo0Iy1F20RvaBuyaUsYTKHJe7tcjIEzFmV2ZmzKnNWZYCZpqotvX3IX8d98P9X_rlpwIcLEFp3xxgWU1wMyQUfl-Cq8Tk-lv8XD3Sj8Q</recordid><startdate>20160815</startdate><enddate>20160815</enddate><creator>Jung, Se-Hui</creator><creator>Kong, Deok-Hoon</creator><creator>Jeon, Hye-Yoon</creator><creator>Ji, Su-Hyun</creator><creator>Han, Eun-Taek</creator><creator>Park, Won Sun</creator><creator>Hong, Seok-Ho</creator><creator>Kim, Min-Soo</creator><creator>Kim, Young-Myeong</creator><creator>Ha, Kwon-Soo</creator><general>Elsevier 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>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7SP</scope><scope>7U5</scope><scope>L7M</scope></search><sort><creationdate>20160815</creationdate><title>Identification of transglutaminase 2 kinase substrates using a novel on-chip activity assay</title><author>Jung, Se-Hui ; Kong, Deok-Hoon ; Jeon, Hye-Yoon ; Ji, Su-Hyun ; Han, Eun-Taek ; Park, Won Sun ; Hong, Seok-Ho ; Kim, Min-Soo ; Kim, Young-Myeong ; Ha, Kwon-Soo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c459t-3269c35b72453c022201c06195999892fcdfd2df74d24903b6ea547754dfc72a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Apoptosis</topic><topic>Arrays</topic><topic>Assaying</topic><topic>Biosensing Techniques - instrumentation</topic><topic>Cellular</topic><topic>Constants</topic><topic>Enzyme Assays - instrumentation</topic><topic>Enzymes</topic><topic>Equipment Design</topic><topic>GTP-Binding Proteins - metabolism</topic><topic>Humans</topic><topic>Kinases</topic><topic>Kinetics</topic><topic>Michaelis-Menten constants (Km)</topic><topic>On-chip TG2 kinase activity assay</topic><topic>Phosphorylation</topic><topic>Protein Array Analysis - instrumentation</topic><topic>Protein Kinases - metabolism</topic><topic>Proteins</topic><topic>Substrate affinity map</topic><topic>Substrate Specificity</topic><topic>Substrates</topic><topic>Transglutaminase 2</topic><topic>Transglutaminases - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jung, Se-Hui</creatorcontrib><creatorcontrib>Kong, Deok-Hoon</creatorcontrib><creatorcontrib>Jeon, Hye-Yoon</creatorcontrib><creatorcontrib>Ji, Su-Hyun</creatorcontrib><creatorcontrib>Han, Eun-Taek</creatorcontrib><creatorcontrib>Park, Won Sun</creatorcontrib><creatorcontrib>Hong, Seok-Ho</creatorcontrib><creatorcontrib>Kim, Min-Soo</creatorcontrib><creatorcontrib>Kim, Young-Myeong</creatorcontrib><creatorcontrib>Ha, Kwon-Soo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Biosensors & bioelectronics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jung, Se-Hui</au><au>Kong, Deok-Hoon</au><au>Jeon, Hye-Yoon</au><au>Ji, Su-Hyun</au><au>Han, Eun-Taek</au><au>Park, Won Sun</au><au>Hong, Seok-Ho</au><au>Kim, Min-Soo</au><au>Kim, Young-Myeong</au><au>Ha, Kwon-Soo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of transglutaminase 2 kinase substrates using a novel on-chip activity assay</atitle><jtitle>Biosensors & bioelectronics</jtitle><addtitle>Biosens Bioelectron</addtitle><date>2016-08-15</date><risdate>2016</risdate><volume>82</volume><spage>40</spage><epage>48</epage><pages>40-48</pages><issn>0956-5663</issn><eissn>1873-4235</eissn><abstract>Transglutaminase 2 (TG2) is an enzyme that plays a critical role in a wide variety of cellular processes through its multifunctional activities. TG2 kinase has emerged as an important regulator of apoptosis, as well as of chromatin structure and function. However, systematic investigation of TG2 kinase substrates is limited due to a lack of a suitable TG2 kinase activity assays. Thus, we developed a novel on-chip TG2 kinase activity assay for quantitative determination of TG2 kinase activity and for screening TG2 kinase substrate proteins in a high-throughput manner. Quantitative TG2 kinase activity was determined by selective detection of substrate protein phosphorylation on the surface of well-type amine arrays. The limit of detection (LOD) of this assay was 4.34μg/ml. We successfully applied this new activity assay to the kinetic analysis of 27 TG2-related proteins for TG2 kinase activity in a high-throughput manner and determined Michaelis-Menten constants (Km) of these proteins. We used the Km values and cellular locations of the TG2-related proteins to construct a substrate affinity map for TG2 kinase. Therefore, this on-chip TG2 kinase activity assay has a strong potential for the systematic investigation of substrate proteins and will be helpful for studying new physiological functions.
•We developed a new on-chip TG2 kinase activity assay.•We successfully applied this activity assay to the kinetic analysis of 27 TG2-related proteins for TG2 kinase activity.•We used the Km values obtained from the large-scale analyses to construct a substrate affinity map for TG2 kinase.•Thus, this on-chip TG2 kinase activity assay has a strong potential for the systematic investigation of substrate proteins.•And will be helpful for studying its new physiological functions.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>27040940</pmid><doi>10.1016/j.bios.2016.03.064</doi><tpages>9</tpages></addata></record> |
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subjects | Apoptosis Arrays Assaying Biosensing Techniques - instrumentation Cellular Constants Enzyme Assays - instrumentation Enzymes Equipment Design GTP-Binding Proteins - metabolism Humans Kinases Kinetics Michaelis-Menten constants (Km) On-chip TG2 kinase activity assay Phosphorylation Protein Array Analysis - instrumentation Protein Kinases - metabolism Proteins Substrate affinity map Substrate Specificity Substrates Transglutaminase 2 Transglutaminases - metabolism |
title | Identification of transglutaminase 2 kinase substrates using a novel on-chip activity assay |
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