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Optimizing fluorophore density for single virus counting: a photophysical approach

Methods and Applications in Fluorescence 2021 9 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 40 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Swarupa Chatterjee, R. Martijn Wagterveld, Swarupa Chatterjee, R. Martijn Wagterveld, Swarupa Chatterjee, Swarupa Chatterjee, Swarupa Chatterjee, Swarupa Chatterjee, Robert Molenaar, Robert Molenaar, Robert Molenaar, Swarupa Chatterjee, Swarupa Chatterjee, Swarupa Chatterjee, Swarupa Chatterjee, Swarupa Chatterjee, Swarupa Chatterjee, Robert Molenaar, R. Martijn Wagterveld, Robert Molenaar, Robert Molenaar, Mireille M. A. E. Claessens, Mireille M. A. E. Claessens, Leroy Tromp, Leroy Tromp, R. Martijn Wagterveld, Mireille M. A. E. Claessens, R. Martijn Wagterveld, Mireille M. A. E. Claessens, Christian Blum Christian Blum H.D.W. Roesink, Mireille M. A. E. Claessens, Christian Blum Christian Blum H.D.W. Roesink, Jeroen J. L. M. Cornelissen, Christian Blum Mireille M. A. E. Claessens, Christian Blum

Summary

Researchers developed a photophysical approach to optimize fluorophore density for counting single virus particles, addressing the challenge of quantifying individual bionanoparticles at very low concentrations relevant to health and environmental monitoring applications.

In health and environmental research, it is often necessary to quantify the concentrations of single (bio) nanoparticles present at very low concentrations. Suitable quantification approaches that rely on counting and tracking of single fluorescently labelled (bio) nanoparticles are often challenging since fluorophore self-quenching limits the maximum particle brightness. Here we study how the number of labels per nanoparticle influences the total brightness of fluorescently labelled cowpea chlorotic mottle virus (CCMV). We analyze in detail the photophysical interplay between the fluorophores on the virus particles. We deduce that the formation of dark aggregates and energy transfer towards these aggregates limits the total particle brightness that can be achieved. We show that by carefully selecting the number of fluorescent labels per CCMV, and thus minimizing the negative effects on particle brightness, it is possible to quantify fluorescently labelled CCMV concentrations down to fM concentrations in single particle counting experiments.

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