Physics
Protein-coat dynamics and cluster phases in intracellular trafficking
Document Type
Article
Abstract
Clustering of membrane proteins is a hallmark of biological membranes' lateral organization and crucial to their function. However, the physical properties of these protein aggregates remain poorly understood. Ensembles of coat proteins, the example considered here, are necessary for intracellular transport in eukaryotic cells. Assembly and disassembly rates for coat proteins involved in intracellular vesicular trafficking must be carefully controlled: their assembly deforms the membrane patch and drives vesicle formation, yet the protein coat must rapidly disassemble after vesiculation. Motivated by recent experimental findings for protein-coat dynamics, we study a dynamical Ising-type model for coat assembly and disassembly, and demonstrate how simple dynamical rules generate a robust, steady-state distribution of protein clusters (corresponding to intermediate budded shapes) and how cluster sizes are controlled by the kinetics. We interpret the results in terms of both vesiculation and the coupling to cargo proteins. © 2011 IOP Publishing Ltd.
Publication Title
Journal of Physics Condensed Matter
Publication Date
9-21-2011
Volume
23
Issue
37
ISSN
0953-8984
DOI
10.1088/0953-8984/23/37/374105
Keywords
biological membranes, cytology
Repository Citation
Huber, Greg; Wang, Hui; and Mukhopadhyay, Ranjan, "Protein-coat dynamics and cluster phases in intracellular trafficking" (2011). Physics. 154.
https://commons.clarku.edu/faculty_physics/154