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Reconstituting membrane fission using a high content and throughput assay

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dc.contributor.author SWAMINATHAN, UMA en_US
dc.contributor.author PUCADYIL, THOMAS J. en_US
dc.date.accessioned 2024-09-20T04:03:36Z
dc.date.available 2024-09-20T04:03:36Z
dc.date.issued 2024-06 en_US
dc.identifier.citation Biochemical Society Transactions, 52(03), 1449–1457. en_US
dc.identifier.issn 0300-5127 en_US
dc.identifier.issn 1470-8752 en_US
dc.identifier.uri https://doi.org/10.1042/BST20231325 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9087
dc.description.abstract Protein-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.iso en en_US
dc.publisher Portland Press en_US
dc.subject Biochemical assays en_US
dc.subject Dynamin superfamily en_US
dc.subject Fluorescence microscopy en_US
dc.subject Membrane tubes en_US
dc.subject Reconstitution en_US
dc.subject 2024 en_US
dc.subject 2024-SEP-WEEK3 en_US
dc.subject TOC-SEP-2024 en_US
dc.title Reconstituting membrane fission using a high content and throughput assay en_US
dc.type Article en_US
dc.contributor.department Dept. of Biology en_US
dc.identifier.sourcetitle Biochemical Society Transactions en_US
dc.publication.originofpublisher Foreign en_US


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