Evaluation of Cell-Based Assays for Steroid Nuclear Receptors Delivered by Recombinant Baculoviruses
The authors describe the use of modified baculoviruses containing mammalian expression cassettes (BacMam technology) in steroid nuclear receptor reporter assays designed for screening and profiling agonist and antagonist compounds. Baculo-viruses were constructed that express full-length human genes...
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creator | Katso, Roy M. Parham, Janet H. Caivano, Matilde Clay, William C. Condreay, J. Patrick Gray, David W. Lindley, Kathryn M. Mason, Sarah J. Rieger, Jennifer Wakes, Nicole C. Cairns, William J. Merrihew, Raymond V. |
description | The authors describe the use of modified baculoviruses containing mammalian expression cassettes (BacMam technology) in steroid nuclear receptor reporter assays designed for screening and profiling agonist and antagonist compounds. Baculo-viruses were constructed that express full-length human genes for mineralocorticoid receptor (MR), glucocorticoid receptor (GR), progesterone receptor A (PR-A), and progesterone receptor B (PR-B) from the cytomegalovirus immediate early promoter. A virus carrying the mouse mammary tumor virus–firefly luciferase (MMTV-Luc) cassette was generated to provide a suitable reporter construct. Feasibility studies with BacMam-MR in single-dose tests of 1000 compounds showed high correlation to the standard transfection-based assay results. Likewise, in dose-response experiments, BacMam-based assays for GR and PR-B produced potency and efficacy values similar to transfection assay results. At various receptor/reporter ratios, the BacMam assays showed good flexibility, demonstrating consistent signal-to-background (S/B) ratios and compound potencies. Increasing transduction time from 24 to 48 h provided no benefit, actually reducing overall assay performance as measured by S/B and Z' values. The BacMam technology was applied in studies of isoforms PR-A and PR-B, which showed similar responses to a series of agonists. Taken together, the results demonstrate the utility of steroid nuclear receptor BacMam constructs for compound screening procedures with high reproducibility, reduced turnaround time, and lower cost. (Journal of Biomolecular Screening 2005:715-724) |
doi_str_mv | 10.1177/1087057105278873 |
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Patrick ; Gray, David W. ; Lindley, Kathryn M. ; Mason, Sarah J. ; Rieger, Jennifer ; Wakes, Nicole C. ; Cairns, William J. ; Merrihew, Raymond V.</creator><creatorcontrib>Katso, Roy M. ; Parham, Janet H. ; Caivano, Matilde ; Clay, William C. ; Condreay, J. Patrick ; Gray, David W. ; Lindley, Kathryn M. ; Mason, Sarah J. ; Rieger, Jennifer ; Wakes, Nicole C. ; Cairns, William J. ; Merrihew, Raymond V.</creatorcontrib><description>The authors describe the use of modified baculoviruses containing mammalian expression cassettes (BacMam technology) in steroid nuclear receptor reporter assays designed for screening and profiling agonist and antagonist compounds. Baculo-viruses were constructed that express full-length human genes for mineralocorticoid receptor (MR), glucocorticoid receptor (GR), progesterone receptor A (PR-A), and progesterone receptor B (PR-B) from the cytomegalovirus immediate early promoter. A virus carrying the mouse mammary tumor virus–firefly luciferase (MMTV-Luc) cassette was generated to provide a suitable reporter construct. Feasibility studies with BacMam-MR in single-dose tests of 1000 compounds showed high correlation to the standard transfection-based assay results. Likewise, in dose-response experiments, BacMam-based assays for GR and PR-B produced potency and efficacy values similar to transfection assay results. At various receptor/reporter ratios, the BacMam assays showed good flexibility, demonstrating consistent signal-to-background (S/B) ratios and compound potencies. Increasing transduction time from 24 to 48 h provided no benefit, actually reducing overall assay performance as measured by S/B and Z' values. The BacMam technology was applied in studies of isoforms PR-A and PR-B, which showed similar responses to a series of agonists. Taken together, the results demonstrate the utility of steroid nuclear receptor BacMam constructs for compound screening procedures with high reproducibility, reduced turnaround time, and lower cost. (Journal of Biomolecular Screening 2005:715-724)</description><identifier>ISSN: 2472-5552</identifier><identifier>ISSN: 1087-0571</identifier><identifier>EISSN: 2472-5560</identifier><identifier>EISSN: 1552-454X</identifier><identifier>DOI: 10.1177/1087057105278873</identifier><identifier>PMID: 16129777</identifier><language>eng</language><publisher>Thousand Oaks, CA: Elsevier Inc</publisher><subject>Animals ; BacMam ; Baculoviridae - genetics ; Baculovirus ; Baculoviruses ; Cell Line ; Cell Line, Tumor ; cell-based assay ; Cercopithecus aethiops ; DNA, Recombinant - genetics ; Genomics ; Human cytomegalovirus ; Humans ; Protein Isoforms - analysis ; Protein Isoforms - genetics ; Protein Isoforms - metabolism ; Receptors ; Receptors, Progesterone - analysis ; Receptors, Progesterone - genetics ; Receptors, Progesterone - metabolism ; Steroid hormones ; steroid nuclear receptor ; Transduction, Genetic ; Transfection</subject><ispartof>Journal of biomolecular screening, 2005-10, Vol.10 (7), p.715-724</ispartof><rights>2005 Society for Laboratory Automation and Screening</rights><rights>COPYRIGHT 2005 Sage Publications, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c498t-4b68248f1c9bf7e8681c432f791600af76d1306f164b937c69d47f4192d9a00b3</citedby><cites>FETCH-LOGICAL-c498t-4b68248f1c9bf7e8681c432f791600af76d1306f164b937c69d47f4192d9a00b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16129777$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Katso, Roy M.</creatorcontrib><creatorcontrib>Parham, Janet H.</creatorcontrib><creatorcontrib>Caivano, Matilde</creatorcontrib><creatorcontrib>Clay, William C.</creatorcontrib><creatorcontrib>Condreay, J. Patrick</creatorcontrib><creatorcontrib>Gray, David W.</creatorcontrib><creatorcontrib>Lindley, Kathryn M.</creatorcontrib><creatorcontrib>Mason, Sarah J.</creatorcontrib><creatorcontrib>Rieger, Jennifer</creatorcontrib><creatorcontrib>Wakes, Nicole C.</creatorcontrib><creatorcontrib>Cairns, William J.</creatorcontrib><creatorcontrib>Merrihew, Raymond V.</creatorcontrib><title>Evaluation of Cell-Based Assays for Steroid Nuclear Receptors Delivered by Recombinant Baculoviruses</title><title>Journal of biomolecular screening</title><addtitle>J Biomol Screen</addtitle><description>The authors describe the use of modified baculoviruses containing mammalian expression cassettes (BacMam technology) in steroid nuclear receptor reporter assays designed for screening and profiling agonist and antagonist compounds. Baculo-viruses were constructed that express full-length human genes for mineralocorticoid receptor (MR), glucocorticoid receptor (GR), progesterone receptor A (PR-A), and progesterone receptor B (PR-B) from the cytomegalovirus immediate early promoter. A virus carrying the mouse mammary tumor virus–firefly luciferase (MMTV-Luc) cassette was generated to provide a suitable reporter construct. Feasibility studies with BacMam-MR in single-dose tests of 1000 compounds showed high correlation to the standard transfection-based assay results. Likewise, in dose-response experiments, BacMam-based assays for GR and PR-B produced potency and efficacy values similar to transfection assay results. At various receptor/reporter ratios, the BacMam assays showed good flexibility, demonstrating consistent signal-to-background (S/B) ratios and compound potencies. Increasing transduction time from 24 to 48 h provided no benefit, actually reducing overall assay performance as measured by S/B and Z' values. The BacMam technology was applied in studies of isoforms PR-A and PR-B, which showed similar responses to a series of agonists. Taken together, the results demonstrate the utility of steroid nuclear receptor BacMam constructs for compound screening procedures with high reproducibility, reduced turnaround time, and lower cost. (Journal of Biomolecular Screening 2005:715-724)</description><subject>Animals</subject><subject>BacMam</subject><subject>Baculoviridae - genetics</subject><subject>Baculovirus</subject><subject>Baculoviruses</subject><subject>Cell Line</subject><subject>Cell Line, Tumor</subject><subject>cell-based assay</subject><subject>Cercopithecus aethiops</subject><subject>DNA, Recombinant - genetics</subject><subject>Genomics</subject><subject>Human cytomegalovirus</subject><subject>Humans</subject><subject>Protein Isoforms - analysis</subject><subject>Protein Isoforms - genetics</subject><subject>Protein Isoforms - metabolism</subject><subject>Receptors</subject><subject>Receptors, Progesterone - analysis</subject><subject>Receptors, Progesterone - genetics</subject><subject>Receptors, Progesterone - metabolism</subject><subject>Steroid hormones</subject><subject>steroid nuclear receptor</subject><subject>Transduction, Genetic</subject><subject>Transfection</subject><issn>2472-5552</issn><issn>1087-0571</issn><issn>2472-5560</issn><issn>1552-454X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1r3DAQhkVpaEKae0_Fp96cjGRZknvbbNK0EBrox1nI0igo2NZWshf231fBSwuFtsxBYnieQZqXkDcULimV8oqCktBKCi2TSsnmBTljXLK6bQW8_HVv2Sm5yPkJAKgUTalX5JQKyjop5Rlxt3szLGYOcaqir7Y4DPW1yeiqTc7mkCsfU_V1xhSDqz4vdkCTqi9ocTfHlKsbHMIeU8H7w3M7jn2YzDRX18YuQ9yHtGTMr8mJN0PGi-N5Tr5_uP22_VjfP9x92m7ua8s7Nde8F4px5antei9RCUUtb5iXHRUAxkvhaAPCU8H7rpFWdI5Lz2nHXGcA-uacvFvn7lL8sWCe9RiyLV8yE8Yla6GEaBSD_4IMGOeMsgJeruCjGVCHycc5GVvK4RhsnNCH0t9QDooJqXgRYBVsijkn9HqXwmjSQVPQz7HpP2MrytvjY5Z-RPdbOIZUgHoFsnlE_RSXNJUt_mvg-5XHsut9wKSzDThZdCGhnbWL4e_yT3G6sDE</recordid><startdate>200510</startdate><enddate>200510</enddate><creator>Katso, Roy M.</creator><creator>Parham, Janet H.</creator><creator>Caivano, Matilde</creator><creator>Clay, William C.</creator><creator>Condreay, J. Patrick</creator><creator>Gray, David W.</creator><creator>Lindley, Kathryn M.</creator><creator>Mason, Sarah J.</creator><creator>Rieger, Jennifer</creator><creator>Wakes, Nicole C.</creator><creator>Cairns, William J.</creator><creator>Merrihew, Raymond V.</creator><general>Elsevier Inc</general><general>Sage Publications</general><general>Sage Publications, Inc</general><scope>6I.</scope><scope>AAFTH</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>7QO</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>200510</creationdate><title>Evaluation of Cell-Based Assays for Steroid Nuclear Receptors Delivered by Recombinant Baculoviruses</title><author>Katso, Roy M. ; Parham, Janet H. ; Caivano, Matilde ; Clay, William C. ; Condreay, J. Patrick ; Gray, David W. ; Lindley, Kathryn M. ; Mason, Sarah J. ; Rieger, Jennifer ; Wakes, Nicole C. ; Cairns, William J. ; Merrihew, Raymond V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c498t-4b68248f1c9bf7e8681c432f791600af76d1306f164b937c69d47f4192d9a00b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>BacMam</topic><topic>Baculoviridae - genetics</topic><topic>Baculovirus</topic><topic>Baculoviruses</topic><topic>Cell Line</topic><topic>Cell Line, Tumor</topic><topic>cell-based assay</topic><topic>Cercopithecus aethiops</topic><topic>DNA, Recombinant - genetics</topic><topic>Genomics</topic><topic>Human cytomegalovirus</topic><topic>Humans</topic><topic>Protein Isoforms - analysis</topic><topic>Protein Isoforms - genetics</topic><topic>Protein Isoforms - metabolism</topic><topic>Receptors</topic><topic>Receptors, Progesterone - analysis</topic><topic>Receptors, Progesterone - genetics</topic><topic>Receptors, Progesterone - metabolism</topic><topic>Steroid hormones</topic><topic>steroid nuclear receptor</topic><topic>Transduction, Genetic</topic><topic>Transfection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Katso, Roy M.</creatorcontrib><creatorcontrib>Parham, Janet H.</creatorcontrib><creatorcontrib>Caivano, Matilde</creatorcontrib><creatorcontrib>Clay, William C.</creatorcontrib><creatorcontrib>Condreay, J. Patrick</creatorcontrib><creatorcontrib>Gray, David W.</creatorcontrib><creatorcontrib>Lindley, Kathryn M.</creatorcontrib><creatorcontrib>Mason, Sarah J.</creatorcontrib><creatorcontrib>Rieger, Jennifer</creatorcontrib><creatorcontrib>Wakes, Nicole C.</creatorcontrib><creatorcontrib>Cairns, William J.</creatorcontrib><creatorcontrib>Merrihew, Raymond V.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of biomolecular screening</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Katso, Roy M.</au><au>Parham, Janet H.</au><au>Caivano, Matilde</au><au>Clay, William C.</au><au>Condreay, J. Patrick</au><au>Gray, David W.</au><au>Lindley, Kathryn M.</au><au>Mason, Sarah J.</au><au>Rieger, Jennifer</au><au>Wakes, Nicole C.</au><au>Cairns, William J.</au><au>Merrihew, Raymond V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of Cell-Based Assays for Steroid Nuclear Receptors Delivered by Recombinant Baculoviruses</atitle><jtitle>Journal of biomolecular screening</jtitle><addtitle>J Biomol Screen</addtitle><date>2005-10</date><risdate>2005</risdate><volume>10</volume><issue>7</issue><spage>715</spage><epage>724</epage><pages>715-724</pages><issn>2472-5552</issn><issn>1087-0571</issn><eissn>2472-5560</eissn><eissn>1552-454X</eissn><abstract>The authors describe the use of modified baculoviruses containing mammalian expression cassettes (BacMam technology) in steroid nuclear receptor reporter assays designed for screening and profiling agonist and antagonist compounds. Baculo-viruses were constructed that express full-length human genes for mineralocorticoid receptor (MR), glucocorticoid receptor (GR), progesterone receptor A (PR-A), and progesterone receptor B (PR-B) from the cytomegalovirus immediate early promoter. A virus carrying the mouse mammary tumor virus–firefly luciferase (MMTV-Luc) cassette was generated to provide a suitable reporter construct. Feasibility studies with BacMam-MR in single-dose tests of 1000 compounds showed high correlation to the standard transfection-based assay results. Likewise, in dose-response experiments, BacMam-based assays for GR and PR-B produced potency and efficacy values similar to transfection assay results. At various receptor/reporter ratios, the BacMam assays showed good flexibility, demonstrating consistent signal-to-background (S/B) ratios and compound potencies. Increasing transduction time from 24 to 48 h provided no benefit, actually reducing overall assay performance as measured by S/B and Z' values. The BacMam technology was applied in studies of isoforms PR-A and PR-B, which showed similar responses to a series of agonists. Taken together, the results demonstrate the utility of steroid nuclear receptor BacMam constructs for compound screening procedures with high reproducibility, reduced turnaround time, and lower cost. (Journal of Biomolecular Screening 2005:715-724)</abstract><cop>Thousand Oaks, CA</cop><pub>Elsevier Inc</pub><pmid>16129777</pmid><doi>10.1177/1087057105278873</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals BacMam Baculoviridae - genetics Baculovirus Baculoviruses Cell Line Cell Line, Tumor cell-based assay Cercopithecus aethiops DNA, Recombinant - genetics Genomics Human cytomegalovirus Humans Protein Isoforms - analysis Protein Isoforms - genetics Protein Isoforms - metabolism Receptors Receptors, Progesterone - analysis Receptors, Progesterone - genetics Receptors, Progesterone - metabolism Steroid hormones steroid nuclear receptor Transduction, Genetic Transfection |
title | Evaluation of Cell-Based Assays for Steroid Nuclear Receptors Delivered by Recombinant Baculoviruses |
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