Identification of leucocyte surface protein interactions by high-throughput screening with multivalent reagents.

We describe a high-throughput screening system to detect interactions between leucocyte surface proteins, taking into account that these interactions are usually of very low affinity. The method involves producing the extracellular regions of leucocyte proteins with tags so that they can be bound to...

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Main Authors: Jiang, L, Barclay, N
Format: Journal article
Language:English
Published: 2010
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author Jiang, L
Barclay, N
author_facet Jiang, L
Barclay, N
author_sort Jiang, L
collection OXFORD
description We describe a high-throughput screening system to detect interactions between leucocyte surface proteins, taking into account that these interactions are usually of very low affinity. The method involves producing the extracellular regions of leucocyte proteins with tags so that they can be bound to nanoparticles to provide an avid reagent to screen over an array of 36 similar proteins immobilized using the Proteon XPR36 with detection by surface plasmon resonance. The system was tested using established interactions that could be detected without spurious binding. The ability to detect new interactions was shown by identifying a new interaction between carcinoembryonic antigen-related cell adhesion molecule 1 and carcinoembryonic antigen-related cell adhesion molecule 8.
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spelling oxford-uuid:74b7ea99-b706-45b1-9208-3b47525a2c3d2022-03-26T20:04:43ZIdentification of leucocyte surface protein interactions by high-throughput screening with multivalent reagents.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:74b7ea99-b706-45b1-9208-3b47525a2c3dEnglishSymplectic Elements at Oxford2010Jiang, LBarclay, NWe describe a high-throughput screening system to detect interactions between leucocyte surface proteins, taking into account that these interactions are usually of very low affinity. The method involves producing the extracellular regions of leucocyte proteins with tags so that they can be bound to nanoparticles to provide an avid reagent to screen over an array of 36 similar proteins immobilized using the Proteon XPR36 with detection by surface plasmon resonance. The system was tested using established interactions that could be detected without spurious binding. The ability to detect new interactions was shown by identifying a new interaction between carcinoembryonic antigen-related cell adhesion molecule 1 and carcinoembryonic antigen-related cell adhesion molecule 8.
spellingShingle Jiang, L
Barclay, N
Identification of leucocyte surface protein interactions by high-throughput screening with multivalent reagents.
title Identification of leucocyte surface protein interactions by high-throughput screening with multivalent reagents.
title_full Identification of leucocyte surface protein interactions by high-throughput screening with multivalent reagents.
title_fullStr Identification of leucocyte surface protein interactions by high-throughput screening with multivalent reagents.
title_full_unstemmed Identification of leucocyte surface protein interactions by high-throughput screening with multivalent reagents.
title_short Identification of leucocyte surface protein interactions by high-throughput screening with multivalent reagents.
title_sort identification of leucocyte surface protein interactions by high throughput screening with multivalent reagents
work_keys_str_mv AT jiangl identificationofleucocytesurfaceproteininteractionsbyhighthroughputscreeningwithmultivalentreagents
AT barclayn identificationofleucocytesurfaceproteininteractionsbyhighthroughputscreeningwithmultivalentreagents