Spatiotemporal modeling and model restructuration approaches in studies of intracellular signalling pathways

"The main focus of the research is to understand the complex phenomena of cell transduction pathways and cell biology in a single cell. Mathematical modeling and experimental evaluation are widely used approaches for this kind of research. Firstly, A multiscale framework for protein-protein interaction has been established using Brownian dynamics algorithm. Sit specific feature, steric collision, diffusion, co-localization and complex formation with time and space has been included in this spatial modeling framework. By implementation of the time adaptive feature in this framework, the computation time reduces in an order of magnitude compared with traditional modeling framework. This multiscale Brownian framework has been used for the investigation FcεRI aggregation which is an important signaling pathway for immune cells. Using the spatial modeling framework, FcεRI aggregation in the presence of trivalent antigen showed consistent results with current experimental studies. Secondly, the rule-based modeling approach is an excellent way of performing large biochemical network modeling for a single cell as it considers the site-specific features. However, the major difficulty of rule-based modeling approach is combinatorial complexity. In this study, model restructuring approaches have been applied to overcome this problem for cell signaling pathway modeling. These mechanistic modeling approaches are very effective to model large network of signaling pathways together without compromising the accuracy. Finally, Cell size dependent cellular uptake study carried out using confocal microscopy and flow cytometer. To understand the particle uptake behavior with time and steady state condition, reaction-diffusion and kinetics model has been developed in these work. After a detailed analysis of experimental data and models, it showed that total particle uptake is increasing with cell size, however, particle flux is reducing in larger cells"--Abstract, page iv.

Name thesis:degree_name

Ph. D. in Chemical Engineering

Grantor

Missouri University of Science and Technology

Author dc:creator

• Shahinuzzaman, Md

• Cell signaling
• Combinatorial complexity
• Diffusion
• Endocytosis
• Ligand- receptor
• Systems biology
• Biomedical Engineering and Bioengineering
• Cell Biology
• Chemical Engineering

Repository record dc:identifier

https://scholarsmine.mst.edu/doctoral_dissertations/2812

OAI identifier oai:identifier

oai:scholarsmine.mst.edu:doctoral_dissertations-3817