Evidence map›Paper›PMID 28985462›Full record

ArticleAnalytical chemistry2017

Reconceptualizing Fluorescence Correlation Spectroscopy for Monitoring and Analyzing Periodically Passing Objects.

Eli Zamir, Christoph Frey, Marian Weiss, Silvia Antona, Johannes P Frohnmayer, Jan-Willi Janiesch, Ilia Platzman, Joachim P Spatz

Abstract read
In one paragraph

Article in Analytical chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Eli ZamirDepartment of Cellular Biophysics, Max Planck Institute for Medical Research , Jahnstraße 29, D-69120 Heidelberg, Germany.
Christoph FreyDepartment of Cellular Biophysics, Max Planck Institute for Medical Research , Jahnstraße 29, D-69120 Heidelberg, Germany.
Marian WeissDepartment of Cellular Biophysics, Max Planck Institute for Medical Research , Jahnstraße 29, D-69120 Heidelberg, Germany.
Silvia AntonaDepartment of Cellular Biophysics, Max Planck Institute for Medical Research , Jahnstraße 29, D-69120 Heidelberg, Germany.
Johannes P FrohnmayerDepartment of Cellular Biophysics, Max Planck Institute for Medical Research , Jahnstraße 29, D-69120 Heidelberg, Germany.
Jan-Willi JanieschDepartment of Cellular Biophysics, Max Planck Institute for Medical Research , Jahnstraße 29, D-69120 Heidelberg, Germany.
Ilia PlatzmanDepartment of Cellular Biophysics, Max Planck Institute for Medical Research , Jahnstraße 29, D-69120 Heidelberg, Germany.
Joachim P SpatzDepartment of Cellular Biophysics, Max Planck Institute for Medical Research , Jahnstraße 29, D-69120 Heidelberg, Germany.ORCID 0000-0003-3419-9807

Funding

European Research Council 294852
6 · The paper itself

Abstract

Fluorescence correlation spectroscopy (FCS) is a sensitive technique commonly applied for studying the dynamics of nanoscale-labeled objects in solution. Current analysis of FCS data is largely based on the assumption that the labeled objects are stochastically displaced due to Brownian motion. However, this assumption is often invalid for microscale objects, since the motion of these objects is dominated by Stokes drag and settling or rising effects, rather than stochastic Brownian motion. To utilize the power of FCS for systems with nonstochastic displacements of objects, the collection and analysis of FCS data have to be reconceptualized. Here, we extended the applicability of FCS for the detection and analysis of periodically passing objects. Toward this end, we implemented droplet-based microfluidics, in which monodispersed droplets containing fluorescent marker are flowing equally spaced within microchannels. We show by simulations and experiments that FCS can sensitively quantify the flow-rates, variability, and content of rapidly passing droplets. This information can be derived at high temporal resolution, based on the intensity fluctuations generated by only 5-10 passing droplets. Moreover, by utilizing the periodicity of the flowing droplets for noise reduction by averaging, FCS can monitor accurately the droplets flow even if their fluorescence intensity is negligible. Hence, extending FCS for periodically passing objects converts it into a powerful analytical tool for high-throughput droplet-based microfluidics. Moreover, based on the principles described here, FCS can be straightforwardly applied for a variety of systems in which the passing of objects is periodic rather than stochastic.

Identifiers

PMID28985462
PMCPMC5677728

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.