ReLo: Analyse direkter Protein-Protein-Interaktionen durch Relokalisation
We have developed a cell-based relocalization (ReLo) assay for the detection of direct protein-protein interactions. In the assay, one protein is anchored to a membrane, causing the other protein to relocalize upon interaction. The assay can be used to study the influence of protein domains, post-tr...
Gespeichert in:
Veröffentlicht in: | Biospektrum 2024-11, Vol.30 (7), p.769-771 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | ger |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 771 |
---|---|
container_issue | 7 |
container_start_page | 769 |
container_title | Biospektrum |
container_volume | 30 |
creator | Miederer, Levi Jeske, Mandy |
description | We have developed a cell-based relocalization (ReLo) assay for the detection of direct protein-protein interactions. In the assay, one protein is anchored to a membrane, causing the other protein to relocalize upon interaction. The assay can be used to study the influence of protein domains, post-translational modifications, protein conformations, and effector molecules on interactions. The ReLo assay requires plasmid transfection and fluorescence microscopy and can handle structurally complex proteins. |
doi_str_mv | 10.1007/s12268-024-2355-y |
format | Article |
fullrecord | <record><control><sourceid>proquest_sprin</sourceid><recordid>TN_cdi_proquest_journals_3132023790</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3132023790</sourcerecordid><originalsourceid>FETCH-LOGICAL-p71y-ad40497054d31af5629c4e4ee5c35ad070e76ec16e702440e58c2d5f9079d1323</originalsourceid><addsrcrecordid>eNpFkEtLw0AUhQdRsNT-AHcB16N3XpmMu1LUFgpK6X4YMjeaJiRxJl3k3zuhindz4NzDfXyE3DN4ZAD6KTLO84ICl5QLpeh0RRasSE7OpbkmCzBSUyhyfUtWMZ4glTDAjVyQ3QH3_XO27lw7Rcx8HbAZMWQfoR-x7uif7rrkumas-w67zJ9D-ZUdsO0b19bRzfYdualcG3H1q0tyfH05brZ0__6226z3dNBsos5LkEaDkl4wV6mcm1KiRFSlUM6DBtQ5lixHnd6RgKoouVeVAW08E1wsycNl7BD67zPG0Z76c0jnRytSH7jQBlKKX1JxCHX3ieE_xcDO0OwFmk1b7AzNTuIHVCxfSA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3132023790</pqid></control><display><type>article</type><title>ReLo: Analyse direkter Protein-Protein-Interaktionen durch Relokalisation</title><source>Springer Nature - Complete Springer Journals</source><creator>Miederer, Levi ; Jeske, Mandy</creator><creatorcontrib>Miederer, Levi ; Jeske, Mandy</creatorcontrib><description>We have developed a cell-based relocalization (ReLo) assay for the detection of direct protein-protein interactions. In the assay, one protein is anchored to a membrane, causing the other protein to relocalize upon interaction. The assay can be used to study the influence of protein domains, post-translational modifications, protein conformations, and effector molecules on interactions. The ReLo assay requires plasmid transfection and fluorescence microscopy and can handle structurally complex proteins.</description><identifier>ISSN: 0947-0867</identifier><identifier>EISSN: 1868-6249</identifier><identifier>DOI: 10.1007/s12268-024-2355-y</identifier><language>ger</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Biochemistry ; Biomedical and Life Sciences ; Fluorescence microscopy ; Human Genetics ; Life Sciences ; Microbiology ; Pharmacology/Toxicology ; Post-translation ; Protein interaction ; Transfection ; Wissenschaft Special</subject><ispartof>Biospektrum, 2024-11, Vol.30 (7), p.769-771</ispartof><rights>The Author(s) 2024</rights><rights>The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-p71y-ad40497054d31af5629c4e4ee5c35ad070e76ec16e702440e58c2d5f9079d1323</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12268-024-2355-y$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12268-024-2355-y$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids></links><search><creatorcontrib>Miederer, Levi</creatorcontrib><creatorcontrib>Jeske, Mandy</creatorcontrib><title>ReLo: Analyse direkter Protein-Protein-Interaktionen durch Relokalisation</title><title>Biospektrum</title><addtitle>Biospektrum</addtitle><description>We have developed a cell-based relocalization (ReLo) assay for the detection of direct protein-protein interactions. In the assay, one protein is anchored to a membrane, causing the other protein to relocalize upon interaction. The assay can be used to study the influence of protein domains, post-translational modifications, protein conformations, and effector molecules on interactions. The ReLo assay requires plasmid transfection and fluorescence microscopy and can handle structurally complex proteins.</description><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Fluorescence microscopy</subject><subject>Human Genetics</subject><subject>Life Sciences</subject><subject>Microbiology</subject><subject>Pharmacology/Toxicology</subject><subject>Post-translation</subject><subject>Protein interaction</subject><subject>Transfection</subject><subject>Wissenschaft Special</subject><issn>0947-0867</issn><issn>1868-6249</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><recordid>eNpFkEtLw0AUhQdRsNT-AHcB16N3XpmMu1LUFgpK6X4YMjeaJiRxJl3k3zuhindz4NzDfXyE3DN4ZAD6KTLO84ICl5QLpeh0RRasSE7OpbkmCzBSUyhyfUtWMZ4glTDAjVyQ3QH3_XO27lw7Rcx8HbAZMWQfoR-x7uif7rrkumas-w67zJ9D-ZUdsO0b19bRzfYdualcG3H1q0tyfH05brZ0__6226z3dNBsos5LkEaDkl4wV6mcm1KiRFSlUM6DBtQ5lixHnd6RgKoouVeVAW08E1wsycNl7BD67zPG0Z76c0jnRytSH7jQBlKKX1JxCHX3ieE_xcDO0OwFmk1b7AzNTuIHVCxfSA</recordid><startdate>20241101</startdate><enddate>20241101</enddate><creator>Miederer, Levi</creator><creator>Jeske, Mandy</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope></search><sort><creationdate>20241101</creationdate><title>ReLo: Analyse direkter Protein-Protein-Interaktionen durch Relokalisation</title><author>Miederer, Levi ; Jeske, Mandy</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p71y-ad40497054d31af5629c4e4ee5c35ad070e76ec16e702440e58c2d5f9079d1323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>ger</language><creationdate>2024</creationdate><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Fluorescence microscopy</topic><topic>Human Genetics</topic><topic>Life Sciences</topic><topic>Microbiology</topic><topic>Pharmacology/Toxicology</topic><topic>Post-translation</topic><topic>Protein interaction</topic><topic>Transfection</topic><topic>Wissenschaft Special</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Miederer, Levi</creatorcontrib><creatorcontrib>Jeske, Mandy</creatorcontrib><collection>Springer Nature OA Free Journals</collection><jtitle>Biospektrum</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Miederer, Levi</au><au>Jeske, Mandy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ReLo: Analyse direkter Protein-Protein-Interaktionen durch Relokalisation</atitle><jtitle>Biospektrum</jtitle><stitle>Biospektrum</stitle><date>2024-11-01</date><risdate>2024</risdate><volume>30</volume><issue>7</issue><spage>769</spage><epage>771</epage><pages>769-771</pages><issn>0947-0867</issn><eissn>1868-6249</eissn><abstract>We have developed a cell-based relocalization (ReLo) assay for the detection of direct protein-protein interactions. In the assay, one protein is anchored to a membrane, causing the other protein to relocalize upon interaction. The assay can be used to study the influence of protein domains, post-translational modifications, protein conformations, and effector molecules on interactions. The ReLo assay requires plasmid transfection and fluorescence microscopy and can handle structurally complex proteins.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><doi>10.1007/s12268-024-2355-y</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0947-0867 |
ispartof | Biospektrum, 2024-11, Vol.30 (7), p.769-771 |
issn | 0947-0867 1868-6249 |
language | ger |
recordid | cdi_proquest_journals_3132023790 |
source | Springer Nature - Complete Springer Journals |
subjects | Biochemistry Biomedical and Life Sciences Fluorescence microscopy Human Genetics Life Sciences Microbiology Pharmacology/Toxicology Post-translation Protein interaction Transfection Wissenschaft Special |
title | ReLo: Analyse direkter Protein-Protein-Interaktionen durch Relokalisation |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T14%3A54%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_sprin&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=ReLo:%20Analyse%20direkter%20Protein-Protein-Interaktionen%20durch%20Relokalisation&rft.jtitle=Biospektrum&rft.au=Miederer,%20Levi&rft.date=2024-11-01&rft.volume=30&rft.issue=7&rft.spage=769&rft.epage=771&rft.pages=769-771&rft.issn=0947-0867&rft.eissn=1868-6249&rft_id=info:doi/10.1007/s12268-024-2355-y&rft_dat=%3Cproquest_sprin%3E3132023790%3C/proquest_sprin%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3132023790&rft_id=info:pmid/&rfr_iscdi=true |