METHODS AND KITS FOR PREDICTING DRUG CARDIOTOXICITY

To provide simple methods for predicting the potential for drug-induced prolongation of action potential duration of ventricular muscle.SOLUTION: Provided is a method for predicting the cardiotoxicity of a test substance, which comprises: expressing a protein in which a hERG channel, a transmembrane...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: HORI AYUMI, YAMAGISHI YUTAKA
Format: Patent
Sprache:eng ; jpn
Schlagworte:
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page
container_title
container_volume
creator HORI AYUMI
YAMAGISHI YUTAKA
description To provide simple methods for predicting the potential for drug-induced prolongation of action potential duration of ventricular muscle.SOLUTION: Provided is a method for predicting the cardiotoxicity of a test substance, which comprises: expressing a protein in which a hERG channel, a transmembrane area, and one fragment of a full-length reporter protein divided into two is fused, on a cell membrane surface; adding the test substance to a medium to culture the cells; removing the test substance, subsequently adding the other fragment of the full-length reporter protein divided into two to reconstitute the full-length reporter protein on the cells; and measuring the signal from the reconstituted reporter protein.SELECTED DRAWING: Figure 10 【課題】 薬剤により引き起こされる心室筋の活動電位持続時間の延長の可能性を予測するための簡易な方法を提供すること。【解決手段】 hERGチャネル、膜貫通領域及び全長レポータータンパク質を2分割した一方のフラグメントを融合させたタンパク質を細胞膜表面上に発現させること、被験物質を培地に添加して前記細胞を培養すること、前記被験物質を除去してから、前記全長レポータータンパク質を2分割した他方のフラグメントを添加して、前記細胞上で前記全長レポータータンパク質を再構成すること、前記再構成されたレポータータンパク質からのシグナルを測定することを含む、被験物質の心毒性を予測する方法。【選択図】 図10
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_JP2021029190A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>JP2021029190A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_JP2021029190A3</originalsourceid><addsrcrecordid>eNrjZDD2dQ3x8HcJVnD0c1Hw9gwJVnDzD1IICHJ18XQO8fRzV3AJCnVXcHYMcvH0D_GP8HT2DInkYWBNS8wpTuWF0twMSm6uIc4euqkF-fGpxQWJyal5qSXxXgFGBkaGBkaWhpYGjsZEKQIA7sQnlQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>METHODS AND KITS FOR PREDICTING DRUG CARDIOTOXICITY</title><source>esp@cenet</source><creator>HORI AYUMI ; YAMAGISHI YUTAKA</creator><creatorcontrib>HORI AYUMI ; YAMAGISHI YUTAKA</creatorcontrib><description>To provide simple methods for predicting the potential for drug-induced prolongation of action potential duration of ventricular muscle.SOLUTION: Provided is a method for predicting the cardiotoxicity of a test substance, which comprises: expressing a protein in which a hERG channel, a transmembrane area, and one fragment of a full-length reporter protein divided into two is fused, on a cell membrane surface; adding the test substance to a medium to culture the cells; removing the test substance, subsequently adding the other fragment of the full-length reporter protein divided into two to reconstitute the full-length reporter protein on the cells; and measuring the signal from the reconstituted reporter protein.SELECTED DRAWING: Figure 10 【課題】 薬剤により引き起こされる心室筋の活動電位持続時間の延長の可能性を予測するための簡易な方法を提供すること。【解決手段】 hERGチャネル、膜貫通領域及び全長レポータータンパク質を2分割した一方のフラグメントを融合させたタンパク質を細胞膜表面上に発現させること、被験物質を培地に添加して前記細胞を培養すること、前記被験物質を除去してから、前記全長レポータータンパク質を2分割した他方のフラグメントを添加して、前記細胞上で前記全長レポータータンパク質を再構成すること、前記再構成されたレポータータンパク質からのシグナルを測定することを含む、被験物質の心毒性を予測する方法。【選択図】 図10</description><language>eng ; jpn</language><subject>BEER ; BIOCHEMISTRY ; CHEMISTRY ; COMPOSITIONS OR TEST PAPERS THEREFOR ; COMPOSITIONS THEREOF ; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES ; CULTURE MEDIA ; ENZYMOLOGY ; MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS ; METALLURGY ; MICROBIOLOGY ; MICROORGANISMS OR ENZYMES ; MUTATION OR GENETIC ENGINEERING ; PROCESSES OF PREPARING SUCH COMPOSITIONS ; PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS ; SPIRITS ; VINEGAR ; WINE</subject><creationdate>2021</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20210301&amp;DB=EPODOC&amp;CC=JP&amp;NR=2021029190A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20210301&amp;DB=EPODOC&amp;CC=JP&amp;NR=2021029190A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>HORI AYUMI</creatorcontrib><creatorcontrib>YAMAGISHI YUTAKA</creatorcontrib><title>METHODS AND KITS FOR PREDICTING DRUG CARDIOTOXICITY</title><description>To provide simple methods for predicting the potential for drug-induced prolongation of action potential duration of ventricular muscle.SOLUTION: Provided is a method for predicting the cardiotoxicity of a test substance, which comprises: expressing a protein in which a hERG channel, a transmembrane area, and one fragment of a full-length reporter protein divided into two is fused, on a cell membrane surface; adding the test substance to a medium to culture the cells; removing the test substance, subsequently adding the other fragment of the full-length reporter protein divided into two to reconstitute the full-length reporter protein on the cells; and measuring the signal from the reconstituted reporter protein.SELECTED DRAWING: Figure 10 【課題】 薬剤により引き起こされる心室筋の活動電位持続時間の延長の可能性を予測するための簡易な方法を提供すること。【解決手段】 hERGチャネル、膜貫通領域及び全長レポータータンパク質を2分割した一方のフラグメントを融合させたタンパク質を細胞膜表面上に発現させること、被験物質を培地に添加して前記細胞を培養すること、前記被験物質を除去してから、前記全長レポータータンパク質を2分割した他方のフラグメントを添加して、前記細胞上で前記全長レポータータンパク質を再構成すること、前記再構成されたレポータータンパク質からのシグナルを測定することを含む、被験物質の心毒性を予測する方法。【選択図】 図10</description><subject>BEER</subject><subject>BIOCHEMISTRY</subject><subject>CHEMISTRY</subject><subject>COMPOSITIONS OR TEST PAPERS THEREFOR</subject><subject>COMPOSITIONS THEREOF</subject><subject>CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES</subject><subject>CULTURE MEDIA</subject><subject>ENZYMOLOGY</subject><subject>MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS</subject><subject>METALLURGY</subject><subject>MICROBIOLOGY</subject><subject>MICROORGANISMS OR ENZYMES</subject><subject>MUTATION OR GENETIC ENGINEERING</subject><subject>PROCESSES OF PREPARING SUCH COMPOSITIONS</subject><subject>PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS</subject><subject>SPIRITS</subject><subject>VINEGAR</subject><subject>WINE</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2021</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZDD2dQ3x8HcJVnD0c1Hw9gwJVnDzD1IICHJ18XQO8fRzV3AJCnVXcHYMcvH0D_GP8HT2DInkYWBNS8wpTuWF0twMSm6uIc4euqkF-fGpxQWJyal5qSXxXgFGBkaGBkaWhpYGjsZEKQIA7sQnlQ</recordid><startdate>20210301</startdate><enddate>20210301</enddate><creator>HORI AYUMI</creator><creator>YAMAGISHI YUTAKA</creator><scope>EVB</scope></search><sort><creationdate>20210301</creationdate><title>METHODS AND KITS FOR PREDICTING DRUG CARDIOTOXICITY</title><author>HORI AYUMI ; YAMAGISHI YUTAKA</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_JP2021029190A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; jpn</language><creationdate>2021</creationdate><topic>BEER</topic><topic>BIOCHEMISTRY</topic><topic>CHEMISTRY</topic><topic>COMPOSITIONS OR TEST PAPERS THEREFOR</topic><topic>COMPOSITIONS THEREOF</topic><topic>CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES</topic><topic>CULTURE MEDIA</topic><topic>ENZYMOLOGY</topic><topic>MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS</topic><topic>METALLURGY</topic><topic>MICROBIOLOGY</topic><topic>MICROORGANISMS OR ENZYMES</topic><topic>MUTATION OR GENETIC ENGINEERING</topic><topic>PROCESSES OF PREPARING SUCH COMPOSITIONS</topic><topic>PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS</topic><topic>SPIRITS</topic><topic>VINEGAR</topic><topic>WINE</topic><toplevel>online_resources</toplevel><creatorcontrib>HORI AYUMI</creatorcontrib><creatorcontrib>YAMAGISHI YUTAKA</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>HORI AYUMI</au><au>YAMAGISHI YUTAKA</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>METHODS AND KITS FOR PREDICTING DRUG CARDIOTOXICITY</title><date>2021-03-01</date><risdate>2021</risdate><abstract>To provide simple methods for predicting the potential for drug-induced prolongation of action potential duration of ventricular muscle.SOLUTION: Provided is a method for predicting the cardiotoxicity of a test substance, which comprises: expressing a protein in which a hERG channel, a transmembrane area, and one fragment of a full-length reporter protein divided into two is fused, on a cell membrane surface; adding the test substance to a medium to culture the cells; removing the test substance, subsequently adding the other fragment of the full-length reporter protein divided into two to reconstitute the full-length reporter protein on the cells; and measuring the signal from the reconstituted reporter protein.SELECTED DRAWING: Figure 10 【課題】 薬剤により引き起こされる心室筋の活動電位持続時間の延長の可能性を予測するための簡易な方法を提供すること。【解決手段】 hERGチャネル、膜貫通領域及び全長レポータータンパク質を2分割した一方のフラグメントを融合させたタンパク質を細胞膜表面上に発現させること、被験物質を培地に添加して前記細胞を培養すること、前記被験物質を除去してから、前記全長レポータータンパク質を2分割した他方のフラグメントを添加して、前記細胞上で前記全長レポータータンパク質を再構成すること、前記再構成されたレポータータンパク質からのシグナルを測定することを含む、被験物質の心毒性を予測する方法。【選択図】 図10</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng ; jpn
recordid cdi_epo_espacenet_JP2021029190A
source esp@cenet
subjects BEER
BIOCHEMISTRY
CHEMISTRY
COMPOSITIONS OR TEST PAPERS THEREFOR
COMPOSITIONS THEREOF
CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES
CULTURE MEDIA
ENZYMOLOGY
MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS
METALLURGY
MICROBIOLOGY
MICROORGANISMS OR ENZYMES
MUTATION OR GENETIC ENGINEERING
PROCESSES OF PREPARING SUCH COMPOSITIONS
PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS
SPIRITS
VINEGAR
WINE
title METHODS AND KITS FOR PREDICTING DRUG CARDIOTOXICITY
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T09%3A51%3A47IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-epo_EVB&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=HORI%20AYUMI&rft.date=2021-03-01&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EJP2021029190A%3C/epo_EVB%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true