Molecular simulation - based analysis of signal transduction system in neuronal cells
| Project/Area Number |
16500245
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Neurochemistry/Neuropharmacology
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| Research Institution | Teikyo University |
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Principal Investigator |
NISHIZAWA Kazuhisa Teikyo University, School of Medicine, Associate Professor, 医学部, 助教授 (00260935)
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| Project Period (FY) |
2004 – 2005
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| Project Status |
Completed (Fiscal Year 2005)
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| Budget Amount *help |
¥3,700,000 (Direct Cost: ¥3,700,000)
Fiscal Year 2005: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 2004: ¥3,200,000 (Direct Cost: ¥3,200,000)
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| Keywords | Molecular dynamics / computational chemistry / シミュレーション / Kチャンネル |
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| Research Abstract |
Our initial goal was molecular dynamics simulation-based study of dynamics of the molecules interacting with PIP2 in presynaptic termini. While we confirmed that molecular orbital calculation and molecular simulations with Gromacs and NAMD packages work on our system, strong interaction due to phosphate groups of PIP2 made the time required for equilibration too long for simulaiton study. Hanatoxin (HaTx) is an ellipsoidal-shaped peptide that binds to the voltage sensor of voltage dependent channels. Of physicochemical interest, HaTx has a ‘ring' of charged residues around its periphery and a hydrophobic protrusion. It has previously been postulated that HaTx binds to and functions on the surface of membranes, but a recent fluorescent-quenching study has implied a fairly deep positioning of HaTx in the lipid bilayer membrane. We carried out numerous molecular dynamic simulations of HaTx1, a well-studied variant of HaTx, in fully hydrated phospholipid bilayers, using two different force
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fields, Gromacs and Charmm. The system reproduced the surface binding mode of HaTx1, in which HaTx1 resided in the extracellular-side (outer) water/membrane interface with the hydrophobic patch of HaTx1 facing the membrane interior. On the other hand, analyses with various parameter settings suggested that the surface binding mode was unstable because of the substantial attractive electrostatic force between HaTx1 and the lipid head groups of the inner (opposite) leaflet. Compared with this electrostatic force, the energetic cost for membrane deformation involving meniscus formation appeared to be small. In an attempt to interpret the quenching data, we consider the possibility of dimpling (meniscus formation) that brings HaTx1 inward (only 〜0.7-0.8 nm above the bilayer center), while accounting for the flexibility of both leaflets of the membrane and the long-range interaction between positively charged residues of the membrane-bound peptide and the polar head groups of the opposite leaflet of the membrane. It is suggested that molecular dynamics simulations taking into account the flexibility of the membrane surface is potentially useful in interpreting the fluorescence-quenching data. Less
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Report
(3 results)
Research Products
(4 results)
