Receptor clustering affects signal transduction at the membrane level in the reaction-limited regime

被引:14
作者
Care, Bertrand R. [1 ,2 ,3 ]
Soula, Hedi A. [2 ,3 ]
机构
[1] Univ Lyon, LIRIS UMR CNRS INSA 5205, F-69621 Villeurbanne, France
[2] INRIA Rhone Alpes, EPI Beagle, F-69603 Villeurbanne, France
[3] Univ Lyon, Inserm UMR1060, F-69621 Villeurbanne, France
来源
PHYSICAL REVIEW E | 2013年 / 87卷 / 01期
关键词
INSULIN-RECEPTOR; LIPID RAFTS; POSSIBLE MECHANISM; BINDING-KINETICS; PLASMA-MEMBRANE; MONTE-CARLO; DIFFUSION; QUANTIFICATION; AMPLIFICATION; ACTIVATION;
D O I
10.1103/PhysRevE.87.012720
中图分类号
O35 [流体力学]; O53 [等离子体物理学];
学科分类号
070204 ; 080103 ; 080704 ;
摘要
Many types of membrane receptors are found to be organized as clusters on the cell surface. We investigate the potential effect of such receptor clustering on the intracellular signal transduction stage. We consider a canonical pathway with a membrane receptor (R) activating a membrane-bound intracellular relay protein (G). We use Monte Carlo simulations to recreate biochemical reactions using different receptor spatial distributions and explore the dynamics of the signal transduction. Results show that activation of G by R is severely impaired by R clustering, leading to an apparent blunted biological effect compared to control. Paradoxically, this clustering decreases the half maximal effective dose (ED50) of the transduction stage, increasing the apparent affinity. We study an example of inter-receptor interaction in order to account for possible compensatory effects of clustering and observe the parameter range in which such interactions slightly counterbalance the loss of activation of G. The membrane receptors' spatial distribution affects the internal stages of signal amplification, suggesting a functional role for membrane domains and receptor clustering independently of proximity-induced receptor-receptor interactions. DOI: 10.1103/PhysRevE.87.012720
引用
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页数:7
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