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DC Field | Value | Language |
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dc.contributor.author | Kumar, Harshit | - |
dc.date.accessioned | 2024-03-22T06:04:26Z | - |
dc.date.available | 2024-03-22T06:04:26Z | - |
dc.date.issued | 2023-04 | - |
dc.identifier.uri | http://hdl.handle.net/123456789/2171 | - |
dc.description | Embargo period | en_US |
dc.description.abstract | Cellular membranes are important targets for many membrane-active peptides and drug compounds. Here we are interested in deciphering how lipid membranes are perturbed by several membrane-active molecules, such as cholesterol and crucial peptides such as α- amylase. We employ phase-separated ternary lipid model membranes in the form of giant unilamellar vesicles (GUVs) to simulate raft-like structures that have been proposed to gov- ern many important processes in plasma membranes (e.g., intracellular singling and traf- ficking). Specifically, we use phase contrast microscopy to interrogate how those membrane additives modulate the phase behaviour of free-standing GUVs and the bending rigidity of the membranes. We quantify these changes in the bending rigidity of the lipid membrane and predict cellular characteristics. | en_US |
dc.language.iso | en | en_US |
dc.publisher | IISER Mohali | en_US |
dc.subject | Lipid Membranes | en_US |
dc.subject | Cholesterol | en_US |
dc.subject | Functional Peptides | en_US |
dc.title | Study of Lipid Membranes Interaction With Cholesterol and Functional Peptides | en_US |
dc.type | Thesis | en_US |
dc.guide | Bhatia, Tripta | en_US |
Appears in Collections: | MS-18 |
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