Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9087
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dc.contributor.authorSWAMINATHAN, UMAen_US
dc.contributor.authorPUCADYIL, THOMAS J.en_US
dc.date.accessioned2024-09-20T04:03:36Z
dc.date.available2024-09-20T04:03:36Z
dc.date.issued2024-06en_US
dc.identifier.citationBiochemical Society Transactions, 52(03), 1449–1457.en_US
dc.identifier.issn0300-5127en_US
dc.identifier.issn1470-8752en_US
dc.identifier.urihttps://doi.org/10.1042/BST20231325en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9087
dc.description.abstractProtein-mediated membrane fission has been analyzed both in bulk and at the single event resolution. Studies on membrane fission in vitro using tethers have provided fundamental insights into the process but are low in throughput. In recent years, supported membrane template (SMrT) have emerged as a facile and convenient assay system for membrane fission. SMrTs provide useful information on intermediates in the pathway to fission and are therefore high in content. They are also high in throughput because numerous fission events can be monitored in a single experiment. This review discusses the utility of SMrTs in providing insights into fission pathways and its adaptation to annotate membrane fission functions in proteins.en_US
dc.language.isoenen_US
dc.publisherPortland Pressen_US
dc.subjectBiochemical assaysen_US
dc.subjectDynamin superfamilyen_US
dc.subjectFluorescence microscopyen_US
dc.subjectMembrane tubesen_US
dc.subjectReconstitutionen_US
dc.subject2024en_US
dc.subject2024-SEP-WEEK3en_US
dc.subjectTOC-SEP-2024en_US
dc.titleReconstituting membrane fission using a high content and throughput assayen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Biologyen_US
dc.identifier.sourcetitleBiochemical Society Transactionsen_US
dc.publication.originofpublisherForeignen_US
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