<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Karapidaki I</submitter><funding>European Research Council</funding><funding>NIGMS NIH HHS</funding><pubmed_abstract>Transgenic markers and tools have revolutionised how we study cells and developing organisms. Some of the elements needed to construct those tools are universally applicable (e.g. fluorescent proteins), while others are species-specific (e.g. cis-regulatory elements driving transcription). Membrane-localising signals that target proteins to the plasma membrane have been identified in several model organisms. Unfortunately, the efficacy of these signals varies greatly across species. To address this problem, we generated a toolkit of 11 membrane-localising tags that can be screened rapidly in diverse organisms. The toolkit includes tags that target the plasma membrane through different mechanisms, including signal peptides, the attachment of lipids, and fusion with lipid-binding domains. Ea</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2024.11.12.623055</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12633465</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Targeting the cell membrane in established and emerging model organisms.</pubmed_title><pmcid>PMC12633465</pmcid><funding_grant_id>101044989</funding_grant_id><funding_grant_id>R01 GM138443</funding_grant_id><pubmed_authors>Zilliox M</pubmed_authors><pubmed_authors>Leclere L</pubmed_authors><pubmed_authors>Ustyantsev K</pubmed_authors><pubmed_authors>Laplace-Builhe B</pubmed_authors><pubmed_authors>Momose T</pubmed_authors><pubmed_authors>Burkhardt P</pubmed_authors><pubmed_authors>Handberg-Thorsager M</pubmed_authors><pubmed_authors>Assaf S</pubmed_authors><pubmed_authors>Pang Y</pubmed_authors><pubmed_authors>Salmon B</pubmed_authors><pubmed_authors>Yasuo H</pubmed_authors><pubmed_authors>Genikhovich G</pubmed_authors><pubmed_authors>Brunet T</pubmed_authors><pubmed_authors>Dickinson DJ</pubmed_authors><pubmed_authors>Karapidaki I</pubmed_authors><pubmed_authors>Averof M</pubmed_authors><pubmed_authors>Deleau C</pubmed_authors><pubmed_authors>Koenig M</pubmed_authors><pubmed_authors>Lohmann B</pubmed_authors><pubmed_authors>Pavlich C</pubmed_authors><pubmed_authors>Stranges M</pubmed_authors><pubmed_authors>Huisken J</pubmed_authors><pubmed_authors>Houliston E</pubmed_authors><pubmed_authors>Colgren JJ</pubmed_authors><pubmed_authors>Arnone MI</pubmed_authors><pubmed_authors>Rusciano ML</pubmed_authors><pubmed_authors>Berezikov E</pubmed_authors><pubmed_authors>Mathieu J</pubmed_authors><pubmed_authors>Bucher G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Targeting the cell membrane in established and emerging model organisms.</name><description>Transgenic markers and tools have revolutionised how we study cells and developing organisms. Some of the elements needed to construct those tools are universally applicable (e.g. fluorescent proteins), while others are species-specific (e.g. cis-regulatory elements driving transcription). Membrane-localising signals that target proteins to the plasma membrane have been identified in several model organisms. Unfortunately, the efficacy of these signals varies greatly across species. To address this problem, we generated a toolkit of 11 membrane-localising tags that can be screened rapidly in diverse organisms. The toolkit includes tags that target the plasma membrane through different mechanisms, including signal peptides, the attachment of lipids, and fusion with lipid-binding domains. Ea</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-07-05T03:14:38.658Z</modification><creation>2026-07-05T03:11:15.124Z</creation></dates><accession>S-EPMC12633465</accession><cross_references><pubmed>41279658</pubmed><doi>10.1101/2024.11.12.623055</doi></cross_references></HashMap>