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Updated: Jul 11, 2026

Rapid Determination of Antibody-Antigen Affinity by Mass Photometry
Published on: February 8, 2021
A dynamical study of antibody-antigen encounter reactions
Lorenzo Bongini1, Duccio Fanelli, Francesco Piazza
1Dipartimento di Fisica, Università di Firenze, V. G. Sansone 1, 50019 Firenze, Italy. bongini@fi.infn.it
Insights
Internal dynamics in macro-molecule encounters, like antigen-antibody reactions, significantly impact molecular biology. This study reveals cooperative behavior in antibodies due to internal dynamics, enhancing binding avidity.
Area of Science:
- Molecular Biology
- Biophysics
- Biochemistry
Background:
- Diffusion-driven encounters between macro-molecules are fundamental in molecular biology.
- Understanding the role of internal molecular dynamics is crucial for reaction efficiency.
Purpose of the Study:
- To investigate the influence of internal dynamics on antigen-antibody reactions.
- To develop a theoretical framework explaining the observed phenomena.
- To quantify avidity enhancement in multi-valent antigen binding.
Main Methods:
- Coarse-grained mechanical modeling parameterized by single-molecule experiments.
- Analytical development of a theoretical framework.
- Numerical simulations of antigen-antibody interactions.
Main Results:
- Internal dynamics are a crucial factor in the diffusion-driven encounter process.
- Antibody internal dynamics lead to cooperative behavior among sub-units.
- Double binding to multi-valent antigens significantly enhances avidity.
Conclusions:
- The internal dynamics of molecules play a critical role in biological interactions.
- Cooperative sub-unit behavior in antibodies enhances binding efficiency.
- The developed model accurately predicts avidity enhancement in multi-valent binding events.
Abstract:
The effects of internal dynamics in diffusion-driven encounters between macro-molecules represent a problem of broad relevance in molecular biology. In this view, we investigate a typical antigen-antibody reaction chain, based on a coarse-grained mechanical model parameterized directly upon results from single-molecule experiments. We demonstrate that the internal dynamics is a crucial factor in the encounter process. To describe our numerical results, we formulate a simple, intuitive theoretical framework, and we develop it analytically. This enables us to show that the inner dynamics of antibody molecules results in a cooperative behavior of their individual sub-units. Along the same lines, we also investigate the case of double binding to multi-valent antigens. Our results quantify the enhancement of avidity afforded by the double binding in excellent agreement with the available experimental data.
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