Making a little affinity go a long way: a topological view of LFA-1 regulation.

Lymphocytes utilize adhesion to navigate in the body and to transiently interact with a variety of potential antigen presenting cells. Interactions of adhesion molecules are governed by the law of mass action and the less understood rules of apposed biological membranes. Biochemical parameters such...

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Main Author: Dustin, M
Format: Journal article
Language:English
Published: 1998
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author Dustin, M
author_facet Dustin, M
author_sort Dustin, M
collection OXFORD
description Lymphocytes utilize adhesion to navigate in the body and to transiently interact with a variety of potential antigen presenting cells. Interactions of adhesion molecules are governed by the law of mass action and the less understood rules of apposed biological membranes. Biochemical parameters such as adhesion molecule affinity only tell part of the story. Factors such as lateral mobility, membrane alignment and cytoskeletal interactions are equally important in determining the final outcome. Therefore it is important to determine mechanisms by which the properties of cell membranes and the cytoskeleton reinforce or hinder adhesion molecule interactions. Work from my lab has shown that one mechanism by which lymphocyte adhesion molecules cooperate is to align adhering membranes with nanometer precision. Here, I discuss a model for LFA-1 regulation that is dependent on three independent processes: LFA-1 lateral mobility, ligand induced generation of a small amount of high affinity LFA-1 and local membrane alignment. I propose that coordination of these processes allows rapid interconversion between stable adhesion and detachment.
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spelling oxford-uuid:72969ae3-928e-4b93-ad43-2eb832840d0b2022-03-26T19:51:08ZMaking a little affinity go a long way: a topological view of LFA-1 regulation.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:72969ae3-928e-4b93-ad43-2eb832840d0bEnglishSymplectic Elements at Oxford1998Dustin, MLymphocytes utilize adhesion to navigate in the body and to transiently interact with a variety of potential antigen presenting cells. Interactions of adhesion molecules are governed by the law of mass action and the less understood rules of apposed biological membranes. Biochemical parameters such as adhesion molecule affinity only tell part of the story. Factors such as lateral mobility, membrane alignment and cytoskeletal interactions are equally important in determining the final outcome. Therefore it is important to determine mechanisms by which the properties of cell membranes and the cytoskeleton reinforce or hinder adhesion molecule interactions. Work from my lab has shown that one mechanism by which lymphocyte adhesion molecules cooperate is to align adhering membranes with nanometer precision. Here, I discuss a model for LFA-1 regulation that is dependent on three independent processes: LFA-1 lateral mobility, ligand induced generation of a small amount of high affinity LFA-1 and local membrane alignment. I propose that coordination of these processes allows rapid interconversion between stable adhesion and detachment.
spellingShingle Dustin, M
Making a little affinity go a long way: a topological view of LFA-1 regulation.
title Making a little affinity go a long way: a topological view of LFA-1 regulation.
title_full Making a little affinity go a long way: a topological view of LFA-1 regulation.
title_fullStr Making a little affinity go a long way: a topological view of LFA-1 regulation.
title_full_unstemmed Making a little affinity go a long way: a topological view of LFA-1 regulation.
title_short Making a little affinity go a long way: a topological view of LFA-1 regulation.
title_sort making a little affinity go a long way a topological view of lfa 1 regulation
work_keys_str_mv AT dustinm makingalittleaffinitygoalongwayatopologicalviewoflfa1regulation