Factors regulating MAPK microdomain dynamics and the flow of spatial information in a spatially restricted neuron signaling network.

An integration of both the experimental data and computational modeling is essential to gain a mechanistic understanding of the complexity in the neuronal signaling network. In-silico approach is applied in this paper to validate the experimental data found from research papers in particular to expl...

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Main Author: Tan, Sock Yee.
Other Authors: School of Chemical and Biomedical Engineering
Format: Final Year Project (FYP)
Language:English
Published: 2012
Subjects:
Online Access:http://hdl.handle.net/10356/50017
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author Tan, Sock Yee.
author2 School of Chemical and Biomedical Engineering
author_facet School of Chemical and Biomedical Engineering
Tan, Sock Yee.
author_sort Tan, Sock Yee.
collection NTU
description An integration of both the experimental data and computational modeling is essential to gain a mechanistic understanding of the complexity in the neuronal signaling network. In-silico approach is applied in this paper to validate the experimental data found from research papers in particular to exploring the neuronal signal information flow. Using Virtual Cell as a computational platform for modeling, it has been proven that factors such as negative regulator e.g. PDE4 together with shape geometry determine the downstream MAPK microdomain which is needed for memory formation. Using the same signaling network model, two more areas of ambiguity are being elucidated. The results have shown that there is a difference between spatial information flow and activity information flow within a signaling network. These two types of information are transmitted through two distinct pathways with the former involving PTP and the latter involving bRaf and MEK. It is also validated that dendritic spine density plays a part in synaptic plasticity. Beside these findings to validate the experimental results, new insights were also found which require further verification by experimental data. These include the interdependency of negative inhibition potential by negative regulators and their location in a neuron signaling pathway, the compensatory effect of increasing dendritic diameter as a result of increasing synaptic plasticity and the last will be that in order for synaptic plasticity to occur, some extent of inhibition on PDE4 is required. All these results provide a basis to pinpointing the exact cause of brain disorders such as Alzheimer’s disease and targeting these impairments without any other unnecessary complications with regard to the ambiguities of the fundamental.
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spelling ntu-10356/500172023-03-03T15:36:17Z Factors regulating MAPK microdomain dynamics and the flow of spatial information in a spatially restricted neuron signaling network. Tan, Sock Yee. School of Chemical and Biomedical Engineering Song Hao DRNTU::Science::Biological sciences::Human anatomy and physiology::Neurobiology An integration of both the experimental data and computational modeling is essential to gain a mechanistic understanding of the complexity in the neuronal signaling network. In-silico approach is applied in this paper to validate the experimental data found from research papers in particular to exploring the neuronal signal information flow. Using Virtual Cell as a computational platform for modeling, it has been proven that factors such as negative regulator e.g. PDE4 together with shape geometry determine the downstream MAPK microdomain which is needed for memory formation. Using the same signaling network model, two more areas of ambiguity are being elucidated. The results have shown that there is a difference between spatial information flow and activity information flow within a signaling network. These two types of information are transmitted through two distinct pathways with the former involving PTP and the latter involving bRaf and MEK. It is also validated that dendritic spine density plays a part in synaptic plasticity. Beside these findings to validate the experimental results, new insights were also found which require further verification by experimental data. These include the interdependency of negative inhibition potential by negative regulators and their location in a neuron signaling pathway, the compensatory effect of increasing dendritic diameter as a result of increasing synaptic plasticity and the last will be that in order for synaptic plasticity to occur, some extent of inhibition on PDE4 is required. All these results provide a basis to pinpointing the exact cause of brain disorders such as Alzheimer’s disease and targeting these impairments without any other unnecessary complications with regard to the ambiguities of the fundamental. Bachelor of Engineering (Chemical and Biomolecular Engineering) 2012-05-28T08:06:01Z 2012-05-28T08:06:01Z 2012 2012 Final Year Project (FYP) http://hdl.handle.net/10356/50017 en Nanyang Technological University 48 p. application/pdf
spellingShingle DRNTU::Science::Biological sciences::Human anatomy and physiology::Neurobiology
Tan, Sock Yee.
Factors regulating MAPK microdomain dynamics and the flow of spatial information in a spatially restricted neuron signaling network.
title Factors regulating MAPK microdomain dynamics and the flow of spatial information in a spatially restricted neuron signaling network.
title_full Factors regulating MAPK microdomain dynamics and the flow of spatial information in a spatially restricted neuron signaling network.
title_fullStr Factors regulating MAPK microdomain dynamics and the flow of spatial information in a spatially restricted neuron signaling network.
title_full_unstemmed Factors regulating MAPK microdomain dynamics and the flow of spatial information in a spatially restricted neuron signaling network.
title_short Factors regulating MAPK microdomain dynamics and the flow of spatial information in a spatially restricted neuron signaling network.
title_sort factors regulating mapk microdomain dynamics and the flow of spatial information in a spatially restricted neuron signaling network
topic DRNTU::Science::Biological sciences::Human anatomy and physiology::Neurobiology
url http://hdl.handle.net/10356/50017
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