In Vitro Cleavage Assays using Purified Recombinant Drosophila Caspases for Substrate Screening
Caspases are very specific cell death proteases that are involved in apoptotic and non-apoptotic processes. While the role of caspases during apoptosis has been very well defined and many apoptotic proteolytic substrates of caspases have been identified and characterized, the role of caspases for no...
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Veröffentlicht in: | Journal of visualized experiments 2022-10 (188) |
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description | Caspases are very specific cell death proteases that are involved in apoptotic and non-apoptotic processes. While the role of caspases during apoptosis has been very well defined and many apoptotic proteolytic substrates of caspases have been identified and characterized, the role of caspases for non-apoptotic processes is not well understood. In particular, few non-apoptotic substrates of caspases have been identified thus far. Here, in order to facilitate the identification and characterization of potential caspase substrates, a protocol that allows the testing of candidate substrates in caspase cleavage assays in vitro is described. This protocol includes the production and purification of recombinant caspase proteins, the production of the candidate substrates either recombinantly or in a cell-free expression system, and the actual in vitro cleavage reaction followed by SDS-PAGE and immunoblotting. This protocol is tailored for the Drosophila caspases Dronc and Drice but can easily be adapted for caspases from other organisms, including mammals. |
doi_str_mv | 10.3791/64392 |
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While the role of caspases during apoptosis has been very well defined and many apoptotic proteolytic substrates of caspases have been identified and characterized, the role of caspases for non-apoptotic processes is not well understood. In particular, few non-apoptotic substrates of caspases have been identified thus far. Here, in order to facilitate the identification and characterization of potential caspase substrates, a protocol that allows the testing of candidate substrates in caspase cleavage assays in vitro is described. This protocol includes the production and purification of recombinant caspase proteins, the production of the candidate substrates either recombinantly or in a cell-free expression system, and the actual in vitro cleavage reaction followed by SDS-PAGE and immunoblotting. This protocol is tailored for the Drosophila caspases Dronc and Drice but can easily be adapted for caspases from other organisms, including mammals.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Caspases - metabolism</subject><subject>Drosophila - metabolism</subject><subject>Drosophila Proteins - metabolism</subject><subject>Mammals - metabolism</subject><subject>Proteolysis</subject><subject>Recombinant Proteins - chemistry</subject><issn>1940-087X</issn><issn>1940-087X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkVtLAzEQhYMo1kv_guRF8GU1t73kSUq9FQqKN3wL2eykjWw3Ndkt-O9dtZb6MMzAfJwZzkFoSMk5zyW9yASXbAcdUClIQor8bXdrHqDDGN8JyRhJi3004BkrWE7TA6QmDX51bfB4XINe6RngUYz6M-IuumaGH7rgrIMKP4Lxi9I1umnxVfDRL-eu1nis41JHiNj6gJ-6MrZBt4CfTABoeoFjtGd1HWG47kfo5eb6eXyXTO9vJ-PRNDGcFW1SyorrLM0tEZktDRGkEFVmDJcV4ZyLykotiQABxhApbZFXKbNGUEmNZYLzI3T5q7vsygVUBpr-kVotg1vo8Km8dur_pnFzNfMrRQlnNBWiVzhbKwT_0UFs1cJFA3WtG_BdVCxnhchEXz16-oua3ogYwG7uUKK-01A_afTcyfZTG-rPfv4FGbiF3A</recordid><startdate>20221006</startdate><enddate>20221006</enddate><creator>Yarikipati, Prathibha</creator><creator>Bergmann, Andreas</creator><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>5PM</scope></search><sort><creationdate>20221006</creationdate><title>In Vitro Cleavage Assays using Purified Recombinant Drosophila Caspases for Substrate Screening</title><author>Yarikipati, Prathibha ; Bergmann, Andreas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c328t-b9d3a657f046fbc04084d6cc39d03334df9a904e4ecc099f87d52fc4191cf2433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Caspases - metabolism</topic><topic>Drosophila - metabolism</topic><topic>Drosophila Proteins - metabolism</topic><topic>Mammals - metabolism</topic><topic>Proteolysis</topic><topic>Recombinant Proteins - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yarikipati, Prathibha</creatorcontrib><creatorcontrib>Bergmann, Andreas</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>PubMed Central (Full Participant titles)</collection><jtitle>Journal of visualized experiments</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Yarikipati, Prathibha</au><au>Bergmann, Andreas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In Vitro Cleavage Assays using Purified Recombinant Drosophila Caspases for Substrate Screening</atitle><jtitle>Journal of visualized experiments</jtitle><addtitle>J Vis Exp</addtitle><date>2022-10-06</date><risdate>2022</risdate><issue>188</issue><issn>1940-087X</issn><eissn>1940-087X</eissn><abstract>Caspases are very specific cell death proteases that are involved in apoptotic and non-apoptotic processes. 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subjects | Animals Apoptosis Caspases - metabolism Drosophila - metabolism Drosophila Proteins - metabolism Mammals - metabolism Proteolysis Recombinant Proteins - chemistry |
title | In Vitro Cleavage Assays using Purified Recombinant Drosophila Caspases for Substrate Screening |
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