Multivalent binding kinetics resolved by fluorescence proximity sensing

Fluorescence proximity sensing enables high throughput determination of binding affinities and kinetics of peptide inhibitors with varying valency and multivalent architecture.

Bibliographic Details
Main Authors: Clemens Schulte, Alice Soldà, Sebastian Spänig, Nathan Adams, Ivana Bekić, Werner Streicher, Dominik Heider, Ralf Strasser, Hans Michael Maric
Format: Article
Language:English
Published: Nature Portfolio 2022-10-01
Series:Communications Biology
Online Access:https://doi.org/10.1038/s42003-022-03997-3
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author Clemens Schulte
Alice Soldà
Sebastian Spänig
Nathan Adams
Ivana Bekić
Werner Streicher
Dominik Heider
Ralf Strasser
Hans Michael Maric
author_facet Clemens Schulte
Alice Soldà
Sebastian Spänig
Nathan Adams
Ivana Bekić
Werner Streicher
Dominik Heider
Ralf Strasser
Hans Michael Maric
author_sort Clemens Schulte
collection DOAJ
description Fluorescence proximity sensing enables high throughput determination of binding affinities and kinetics of peptide inhibitors with varying valency and multivalent architecture.
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spelling doaj.art-8429778c1c484c93995699e093705efa2022-12-22T02:26:27ZengNature PortfolioCommunications Biology2399-36422022-10-015111010.1038/s42003-022-03997-3Multivalent binding kinetics resolved by fluorescence proximity sensingClemens Schulte0Alice Soldà1Sebastian Spänig2Nathan Adams3Ivana Bekić4Werner Streicher5Dominik Heider6Ralf Strasser7Hans Michael Maric8Rudolf Virchow Center, Center for Integrative and Translational Bioimaging, University of WuerzburgDynamic Biosensors GmbH GermanyDepartment of Bioinformatics, Faculty of Mathematics and Computer Science, Philipps-University of MarburgNanotemper Technologies GmbHNanotemper Technologies GmbHNanotemper Technologies GmbHDepartment of Bioinformatics, Faculty of Mathematics and Computer Science, Philipps-University of MarburgDynamic Biosensors GmbH GermanyRudolf Virchow Center, Center for Integrative and Translational Bioimaging, University of WuerzburgFluorescence proximity sensing enables high throughput determination of binding affinities and kinetics of peptide inhibitors with varying valency and multivalent architecture.https://doi.org/10.1038/s42003-022-03997-3
spellingShingle Clemens Schulte
Alice Soldà
Sebastian Spänig
Nathan Adams
Ivana Bekić
Werner Streicher
Dominik Heider
Ralf Strasser
Hans Michael Maric
Multivalent binding kinetics resolved by fluorescence proximity sensing
Communications Biology
title Multivalent binding kinetics resolved by fluorescence proximity sensing
title_full Multivalent binding kinetics resolved by fluorescence proximity sensing
title_fullStr Multivalent binding kinetics resolved by fluorescence proximity sensing
title_full_unstemmed Multivalent binding kinetics resolved by fluorescence proximity sensing
title_short Multivalent binding kinetics resolved by fluorescence proximity sensing
title_sort multivalent binding kinetics resolved by fluorescence proximity sensing
url https://doi.org/10.1038/s42003-022-03997-3
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