Literature DB >> 35367423

Simulation of receptor triggering by kinetic segregation shows role of oligomers and close contacts.

Robert Taylor1, Jun Allard2, Elizabeth L Read3.   

Abstract

The activation of T cells, key players of the immune system, involves local evacuation of phosphatase CD45 from a region of the T cell's surface, segregating it from the T cell receptor. What drives this evacuation? In the presence of antigen, what ensures evacuation happens in the subsecond timescales necessary to initiate signaling? In the absence of antigen, what mechanisms ensure that evacuation does not happen spontaneously, which could cause signaling errors? Phenomena known to influence spatial organization of CD45 or similar surface molecules include diffusive motion in the lipid bilayer, oligomerization reactions, and mechanical compression against a nearby surface, such as that of the cell presenting the antigen. Computer simulations can investigate hypothesized spatiotemporal mechanisms of T cell signaling. The challenge to computational studies of evacuation is that the base process, spontaneous evacuation by simple diffusion, is in the extreme rare event limit, meaning direct stochastic simulation is unfeasible. Here, we combine particle-based spatial stochastic simulation with the weighted ensemble method for rare events to compute the mean first passage time for cell surface availability by surface reorganization of CD45. We confirm mathematical estimates that, at physiological concentrations, spontaneous evacuation is extremely rare, roughly 300 years. We find that dimerization decreases the time required for evacuation. A weak bimolecular interaction (dissociation constant estimate 460 μM) is sufficient for an order of magnitude reduction of spontaneous evacuation times, and oligomerization to hexamers reduces times to below 1 s. This introduces a mechanism whereby externally induced CD45 oligomerization could significantly modify T cell function. For large regions of close contact, such as those induced by large microvilli, molecular size and compressibility imply a nonzero reentry probability of 60%, decreasing evacuation times. Simulations show that these reduced evacuation times are still unrealistically long (even with a fourfold variation centered around previous estimates of parameters), suggesting that a yet-to-be-described mechanism, besides compressional exclusion at a close contact, drives evacuation.
Copyright © 2022 Biophysical Society. Published by Elsevier Inc. All rights reserved.

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Year:  2022        PMID: 35367423      PMCID: PMC9117938          DOI: 10.1016/j.bpj.2022.03.033

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   3.699


  78 in total

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Authors:  Yunmin Jung; Inbal Riven; Sara W Feigelson; Elena Kartvelishvily; Kazuo Tohya; Masayuki Miyasaka; Ronen Alon; Gilad Haran
Journal:  Proc Natl Acad Sci U S A       Date:  2016-09-19       Impact factor: 11.205

7.  Catch Bonds at T Cell Interfaces: Impact of Surface Reorganization and Membrane Fluctuations.

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Journal:  Biophys J       Date:  2017-07-11       Impact factor: 4.033

8.  Nanoclusters of GPI-anchored proteins are formed by cortical actin-driven activity.

Authors:  Debanjan Goswami; Kripa Gowrishankar; Sameera Bilgrami; Subhasri Ghosh; Riya Raghupathy; Rahul Chadda; Ram Vishwakarma; Madan Rao; Satyajit Mayor
Journal:  Cell       Date:  2008-12-12       Impact factor: 41.582

9.  Accurate particle-based simulation of adsorption, desorption and partial transmission.

Authors:  Steven S Andrews
Journal:  Phys Biol       Date:  2009-11-12       Impact factor: 2.583

10.  Confined diffusion of transmembrane proteins and lipids induced by the same actin meshwork lining the plasma membrane.

Authors:  Takahiro K Fujiwara; Kokoro Iwasawa; Ziya Kalay; Taka A Tsunoyama; Yusuke Watanabe; Yasuhiro M Umemura; Hideji Murakoshi; Kenichi G N Suzuki; Yuri L Nemoto; Nobuhiro Morone; Akihiro Kusumi
Journal:  Mol Biol Cell       Date:  2016-02-10       Impact factor: 4.138

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