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B cell receptors and free antibodies have different antigen-binding kinetics

M. Castro, J. Faro

XVIII International Congress of the Spanish Biophysical Society - SBE 2025, Madrid (Spain). 24-27 June 2025


Summary:

Receptor binding and triggering are central in Immunology as T cells activated through their T cell receptors (TCR) by protein antigens orchestrate immune responses. In order to understand receptor ligand
interactions, many groups working with different experimental techniques and assays have generated a vast body of knowledge during the last decades. However, in recent years a type of assays, referred to as two-dimensional or membrane-to-membrane [1], has questioned our current understanding of the role of different kinetic constants (for instance, on- versus off-rate constants) on TCR-ligand interaction and subsequent T cell activation. Here we present a general mathematical framework that provides a unifying umbrella to relate fundamental and effective (or experimentally determined) kinetic constants, as well as describe and compare state-of-the-art experimental methods [2].
On the other hand, in vivo, B cell receptor (BCR)–antigen interactions occur in a 2-dimensional (2D) environment with antigen anchored to a membrane. Conversely, antibody–antigen interactions typically occur in a 3-dimensional (3D) environment [3]. The rotation necessary for the reactive sites (paratope in BCR and antibody and epitope in antigen) to align is a crucial factor in the binding reaction’s kinetic rates, but its impact has been underestimated and currently is unknown. Combining theory and existing empirical data, our study provides the first estimation of approximate 2D and 3D global rotational rates of BCR and antibody paratopes and estimates of 2D and 3D effective kinetic rates based on intrinsic binding rates. Our work also allows to estimate unavailable 2D rates from existing 3D data [4].


Spanish layman's summary:

Esta charla presenta una teoría unificada de cómo los receptores T y B se unen a antígenos en entornos 2D vs 3D, revelando el papel ignorado de la rotación en la cinética de activación inmune.


English layman's summary:

This talk presents a unified theory on how T and B cell receptors bind antigens in 2D vs 3D environments, revealing the overlooked role of rotational alignment in immune activation kinetics.


Keywords: TCR, BCR, antigen binding, 2D vs 3D kinetics, rotational rates, immune response, kinetic constants, membrane interactions


Publication date: 24-Jun-2025.


Citation:
M. Castro, J. Faro, "B cell receptors and free antibodies have different antigen-binding kinetics", presented at XVIII International Congress of the Spanish Biophysical Society - SBE 2025, Madrid, Spain, 24-27 June 2025

    Research groups:
  • Instituto de Investigación Tecnológica (IIT)
  • Dinámica No Lineal
    ODS:
  • Goal 3: Health and well-being

IIT-25-215C_abstract

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