Evidence map›Paper›PMID 42039536›Full record

ArticlebioRxiv : the preprint server for biology2026

Precise Alternation Between Image-Forming Sample Planes Enables Quantitative Monitoring of Receptor-Arrestin Interaction Dynamics at the Plasma Membrane of Live Cells.

Thomas D Killeen, Michael R Stoneman, Ionel Popa, Qiuyan Chen, Valerică Raicu

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

5 authors.

Thomas D KilleenDepartment of Physics & Astronomy, University of Wisconsin-Milwaukee, Milwaukee, WI 53211, USA.ORCID 0009-0006-3997-4648
Michael R StonemanDepartment of Physics & Astronomy, University of Wisconsin-Milwaukee, Milwaukee, WI 53211, USA.ORCID 0000-0002-7060-645X
Ionel PopaDepartment of Physics & Astronomy, University of Wisconsin-Milwaukee, Milwaukee, WI 53211, USA.ORCID 0000-0003-3111-4716
Qiuyan ChenDepartment of Biochemistry, Molecular Biology and Pharmacology, Indiana University School of Medicine; Indianapolis, IN 46202, USA.ORCID 0000-0002-6263-6843
Valerică RaicuDepartment of Physics & Astronomy, University of Wisconsin-Milwaukee, Milwaukee, WI 53211, USA.ORCID 0000-0002-3427-8516

Funding

Structural Basis and Molecular Mechanism of GPCR-Arrestin InteractionsR35GM151033 · NIGMS · INDIANA UNIVERSITY INDIANAPOLIS · PI Qiuyan Chen · 2023 to 2026
$1.6M
NIGMS NIH HHS R35 GM151033
6 · The paper itself

Abstract

Investigations of G protein-coupled receptors (GPCRs) interactions with non-visual arrestins in living cells are essential to understanding the complex molecular mechanisms of GPCR-based signaling. Quantitative analysis of these interactions remains challenging in live cells, particularly when attempting to repeatedly image distinct cellular regions with high precision. Here, we describe the implementation of an optical imaging stabilization approach that integrates the recently developed Focal Readjustment for Enhanced Vertical Resolution (FREVR) technology into a multiphoton microscope, enabling high-precision alternation between image-forming sample planes with < 20-nanometer repeatability and stability over time. Using this setup, we monitored the dynamic recruitment of arrestin-2 (Arr2) to the plasma membrane of HEK-293 cells expressing muscarinic acetylcholine M

Indexed as

arrestinaxial positioningFluorescence microscopyGPCRimage stabilizationlive-cell imaging

Identifiers

PMID42039536
PMCPMC13104873

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.