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

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 timesca...

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Detalles Bibliográficos
Autores principales: Taylor, Robert, Allard, Jun, Read, Elizabeth L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Biophysical Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9117938/
https://www.ncbi.nlm.nih.gov/pubmed/35367423
http://dx.doi.org/10.1016/j.bpj.2022.03.033
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author Taylor, Robert
Allard, Jun
Read, Elizabeth L.
author_facet Taylor, Robert
Allard, Jun
Read, Elizabeth L.
author_sort Taylor, Robert
collection PubMed
description 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.
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spelling pubmed-91179382023-05-03 Simulation of receptor triggering by kinetic segregation shows role of oligomers and close contacts Taylor, Robert Allard, Jun Read, Elizabeth L. Biophys J Articles 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. The Biophysical Society 2022-05-03 2022-03-31 /pmc/articles/PMC9117938/ /pubmed/35367423 http://dx.doi.org/10.1016/j.bpj.2022.03.033 Text en © 2022 Biophysical Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Articles
Taylor, Robert
Allard, Jun
Read, Elizabeth L.
Simulation of receptor triggering by kinetic segregation shows role of oligomers and close contacts
title Simulation of receptor triggering by kinetic segregation shows role of oligomers and close contacts
title_full Simulation of receptor triggering by kinetic segregation shows role of oligomers and close contacts
title_fullStr Simulation of receptor triggering by kinetic segregation shows role of oligomers and close contacts
title_full_unstemmed Simulation of receptor triggering by kinetic segregation shows role of oligomers and close contacts
title_short Simulation of receptor triggering by kinetic segregation shows role of oligomers and close contacts
title_sort simulation of receptor triggering by kinetic segregation shows role of oligomers and close contacts
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9117938/
https://www.ncbi.nlm.nih.gov/pubmed/35367423
http://dx.doi.org/10.1016/j.bpj.2022.03.033
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