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http://hdl.handle.net/123456789/713
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DC Field | Value | Language |
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dc.contributor.author | George, Tara | - |
dc.date.accessioned | 2016-09-14T05:12:07Z | - |
dc.date.available | 2016-09-14T05:12:07Z | - |
dc.date.issued | 2016-09-07 | - |
dc.identifier.uri | http://hdl.handle.net/123456789/713 | - |
dc.description.abstract | We studied the diffusion of amyloid beta peptide(25-35) inside bicelle using Pulse field gradient(PFG) Nuclear Magnetic Resonance(NMR) and molecular dynamics sim- ulations. Amyloid beta peptide(A) is the main constituent of senile plaque in the Alzheimer's disease. The neurotoxic fragment Aβ(25-35) can intercalate into the lipid bilayers and affect the dynamics of bilayers. PFG NMR experiments were conducted for samples Aβ(25-35), bicelle(DMPC/DHPC) and Aβ(25-35) inside bicelle. We cal- culated the diffusion coefficient for Aβ(25-35), bicelle(DMPC/DHPC) and Aβ(25-35) inside bicelle. A linear diffusion pattern was observed for Aβ(25-35) as well as bi- celle alone samples. But when we incorporated Aβ(25-35) into bicelle both systems were following anomalous diffusion . The NMR experiment results were validated by molecular dynamics simulations using the MD package Groningen Machine for Chem- ical Simulations(GROMACS). We did 2-dimensional homonuclear and heteronuclear NMR experiments for studying the structure of Aβ(25-35) in bicelle. | en_US |
dc.description.sponsorship | IISER-M | en_US |
dc.language.iso | en | en_US |
dc.publisher | IISER-M | en_US |
dc.subject | Chemistry | en_US |
dc.subject | NMR | en_US |
dc.subject | Nuclear Magnetic Resonance | en_US |
dc.subject | Amyloid Beta Peptide | en_US |
dc.title | Diffusion Studies of Amyloid Beta Peptide in Bicelle | en_US |
dc.type | Thesis | en_US |
Appears in Collections: | MS-10 |
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File | Description | Size | Format | |
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MS-10076.pdf | 50.89 kB | Adobe PDF | View/Open |
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