Evidence map›Paper›PMID 42847412›Full record

ArticleFEBS open bio2026

Using fluorescence fluctuation spectroscopy to quantify molecular dynamics within cells.

Mark A Hink

Abstract read
In one paragraph

Article in FEBS open bio, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Mark A Hinkvan Leeuwenhoek Centre for Advanced Microscopy, Molecular Cytology, University of Amsterdam, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Originally developed for the field of physical chemistry, fluorescence fluctuation spectroscopy (FFS) has evolved into a family of methods to quantify concentrations, diffusion rates and interactions of fluorescently labeled molecules. Combining microscopy with the ability to measure molecules at the nanomolar level allows for the study of biological processes with high sensitivity even within the living cell. In this protocol, the principles of how to set up these types of experiments are described including calibration samples, challenges and specific cellular applications. The predecessor to FFS, fluorescence correlation spectroscopy (FCS) will be discussed which measures diffusion and concentrations at a user-defined point within the cell. Furthermore, an imaging variant, number and brightness analysis (N&B), will be shown that can be used to quantify molecular oligomerization. Overall, this protocol provides a foundation for using FFS and associated techniques to examine molecular dynamics within cells.

Indexed as

concentrationfluorescence correlation spectroscopyintracellular measurementsmobilitynumber and brightnessoligomerization

Identifiers

PMID42847412
PMCPMC13647958

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.