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|Title:||Comparison of DNA force fields at a multiscale level : towards bottom-up modelling of chromatin||Authors:||Minhas, Vishal||Keywords:||Science::Biological sciences::Biophysics||Issue Date:||2020||Publisher:||Nanyang Technological University||Source:||Minhas, V. (2020). Comparison of DNA force fields at a multiscale level : towards bottom-up modelling of chromatin. Doctoral thesis, Nanyang Technological University, Singapore.||Abstract:||Computer simulations were performed to understand the dynamics of DNA molecules in presence of mono-valent cations. These simulations were run using different allatom DNA force fields to study their behaviour at a multiscale level, from the base-pair to the mesoscopic level. Serious problems were found with the latest version of the CHARMM family of force fields, namely CHARMM36, as it distorted DNA structure and backbone at the microsecond timescale. Also, to achieve the long-term goal of modelling the folding of the chromatin fiber, we have built a multiscale model using systematic bottom-up approach based on structure based coarse-graining. At the first stage of bottom-up coarse-graining, all-atom and mesoatom representations of all principal chromatin components were bridged. To do this, the all-atom molecular dynamics trajectories obtained were bead-mapped to a coarse-grained representation and used for the calculation of the radial distribution functions, which were then used to derive the effective potentials using the Inverse Monte-Carlo method. These potentials were then validated in a coarsegrained molecular dynamics simulation of the original system. Based on these potentials, an excellent prediction of the dependence of DNA persistence length on salt concentration, in agreement with experiments was obtained, which validates the underlying CG-model. Once all the potentials are obtained for all the interactions, a large-scale CG simulation will be run using these potentials to model the NCP.||URI:||https://hdl.handle.net/10356/142499||Rights:||This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).||Fulltext Permission:||open||Fulltext Availability:||With Fulltext|
|Appears in Collections:||SBS Theses|
checked on Oct 23, 2020
checked on Oct 23, 2020
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