<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hsu YY</submitter><funding>University of Michigan</funding><funding>NIBIB NIH HHS</funding><funding>National Institute of General Medical Sciences</funding><funding>NIGMS NIH HHS</funding><funding>National Institute of Biomedical Imaging and Bioengineering</funding><pagination>12-18</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10028359</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(1)</volume><pubmed_abstract>Plasma membrane tension functions as a global physical organizer of cellular activities. Technical limitations of current membrane tension measurement techniques have hampered in-depth investigation of cellular membrane biophysics and the role of plasma membrane tension in regulating cellular processes. Here, we develop an optical membrane tension reporter by repurposing an &lt;i>E. coli&lt;/i> mechanosensitive channel via insertion of circularly permuted GFP (cpGFP), which undergoes a large conformational rearrangement associated with channel activation and thus fluorescence intensity changes under increased membrane tension.</pubmed_abstract><journal>ACS sensors</journal><pubmed_title>Mechanosensitive Channel-Based Optical Membrane Tension Reporter.</pubmed_title><pmcid>PMC10028359</pmcid><funding_grant_id>R21 GM134157</funding_grant_id><funding_grant_id>R01 EB030031</funding_grant_id><funding_grant_id>R01EB030031</funding_grant_id><funding_grant_id>R21GM 134167</funding_grant_id><funding_grant_id>R21 GM103467</funding_grant_id><pubmed_authors>Hsu YY</pubmed_authors><pubmed_authors>Fu J</pubmed_authors><pubmed_authors>Liu AP</pubmed_authors><pubmed_authors>Resto Irizarry AM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mechanosensitive Channel-Based Optical Membrane Tension Reporter.</name><description>Plasma membrane tension functions as a global physical organizer of cellular activities. Technical limitations of current membrane tension measurement techniques have hampered in-depth investigation of cellular membrane biophysics and the role of plasma membrane tension in regulating cellular processes. Here, we develop an optical membrane tension reporter by repurposing an &lt;i>E. coli&lt;/i> mechanosensitive channel via insertion of circularly permuted GFP (cpGFP), which undergoes a large conformational rearrangement associated with channel activation and thus fluorescence intensity changes under increased membrane tension.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-18T15:29:30.764Z</modification><creation>2025-04-07T02:10:33.094Z</creation></dates><accession>S-EPMC10028359</accession><cross_references><pubmed>36608338</pubmed><doi>10.1021/acssensors.2c01921</doi></cross_references></HashMap>