Quantitative understanding of cell signaling: the importance of membrane organization

被引:33
|
作者
Radhakrishnan, Krishnan [2 ,3 ]
Halasz, Adam [4 ,5 ]
Vlachos, Dion [6 ]
Edwards, Jeremy S. [1 ,7 ]
机构
[1] Univ New Mexico, Dept Chem & Nucl Engn, Albuquerque, NM 87131 USA
[2] Univ New Mexico, Hlth Sci Ctr, Dept Pathol, Albuquerque, NM 87131 USA
[3] Univ New Mexico, Hlth Sci Ctr, Ctr Canc, Albuquerque, NM 87131 USA
[4] W Virginia Univ, Dept Math, Morgantown, WV 26506 USA
[5] W Virginia Univ, Mary Babb Randolph Canc Ctr, Morgantown, WV 26506 USA
[6] Univ Delaware, Dept Chem Engn, Newark, DE 19716 USA
[7] Univ New Mexico, Hlth Sci Ctr, Mol Genet & Microbiol & Canc Res & Treatment Ctr, Albuquerque, NM 87131 USA
关键词
SINGLE-MOLECULE TECHNIQUES; PROTEIN-COUPLED RECEPTOR; PLASMA-MEMBRANE; LIPID RAFTS; STOCHASTIC SIMULATIONS; LIGAND-BINDING; CROSS-LINKING; RATE-CONSTANT; IN-SILICO; DIFFUSION;
D O I
10.1016/j.copbio.2010.08.006
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Systems biology modeling of signal transduction pathways traditionally employs ordinary differential equations, deterministic models based on the assumptions of spatial homogeneity. However, this can be a poor approximation for certain aspects of signal transduction, especially its initial steps: the cell membrane exhibits significant spatial organization, with diffusion rates approximately two orders of magnitude slower than those in the cytosol. Thus, to unravel the complexities of signaling pathways, quantitative models must consider spatial organization as an important feature of cell signaling. Furthermore, spatial separation limits the number of molecules that can physically interact, requiring stochastic simulation methods that account for individual molecules. Herein, we discuss the need for mathematical models and experiments that appreciate the importance of spatial organization in the membrane.
引用
收藏
页码:677 / 682
页数:6
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