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Updated: Mar 24, 2026

A Fluorescence Fluctuation Spectroscopy Assay of Protein-Protein Interactions at Cell-Cell Contacts
Published on: December 1, 2018
Fluctuations, Correlations and the Estimation of Concentrations inside Cells
Emiliano Pérez Ipiña1, Silvina Ponce Dawson1
1Departamento de Física, FCEN-UBA, and IFIBA, CONICET, Ciudad Universitaria, Pabellón I, (1428) Buenos Aires, Argentina.
Cellular information transmission is accurate due to binding site dynamics. Fluctuations in bound molecules reveal distinct timescales, explaining transcriptional and enzyme activity variations.
Area of Science:
- Cellular and Molecular Biophysics
- Biochemical Kinetics
- Systems Biology
Background:
- Cellular information transmission relies on ligand-receptor interactions.
- Accurate signaling persists despite fluctuations in molecular concentrations.
- Understanding these fluctuations is key to cellular function.
Purpose of the Study:
- To analyze ligand number and site occupancy fluctuations beyond asymptotic decay.
- To investigate the timescales of bound molecule number decay.
- To correlate fluctuation dynamics with cellular activities like transcription and enzyme kinetics.
Main Methods:
- Mathematical modeling of ligand diffusion and reaction kinetics.
- Analysis of fluctuations in bound molecule numbers and site occupancy.
- Examination of transient and asymptotic decay behaviors.
Main Results:
- Fluctuations in bound molecules for immobile sites decay rapidly before reaching asymptotic behavior.
- The initial decay exhibits one or two timescales, dependent on free ligand concentration.
- This dynamic behavior explains the coexistence of high instantaneous transcriptional activity with low mRNA noise.
Conclusions:
- Cellular signaling accuracy is maintained by rapid decay of binding fluctuations.
- Characteristic timescales in fluctuation decay provide insights into enzyme activity regulation.
- The study offers a mechanistic explanation for observed cellular noise levels and activity dynamics.
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