Evidence map›Paper›PMID 39198447›Full record

ArticleNature communications2024

Label-free, real-time monitoring of membrane binding events at zeptomolar concentrations using frequency-locked optical microresonators.

Adley Gin, Phuong-Diem Nguyen, Jeffrey E Melzer, Cheng Li, Hannah Strzelinski, Stephen B Liggett, Judith Su

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Sub-parts-per-billion CONature communications · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Adley Gin *Wyant College of Optical Sciences, The University of Arizona, Tucson, AZ, 85721, USA.
Phuong-Diem Nguyen *Department of Biomedical Engineering, The University of Arizona, Tucson, AZ, 85721, USA.
Jeffrey E MelzerWyant College of Optical Sciences, The University of Arizona, Tucson, AZ, 85721, USA.
Cheng LiWyant College of Optical Sciences, The University of Arizona, Tucson, AZ, 85721, USA.
Hannah StrzelinskiDepartment of Medicine, University of South Florida Morsani College of Medicine, Tampa, FL, 33612, USA.ORCID 0000-0002-8461-7061
Stephen B LiggettDepartment of Medicine, University of South Florida Morsani College of Medicine, Tampa, FL, 33612, USA.ORCID 0000-0002-0128-3669
Judith SuWyant College of Optical Sciences, The University of Arizona, Tucson, AZ, 85721, USA. judy@optics.arizona.edu.ORCID 0000-0002-1005-1755

Funding

Project 4 - OGR1- and TSPO- dependent mechanisms mediated by benzodiazepines affecting ASM contractionP01HL114471 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI LIGGETT, STEPHEN B · 2013 to 2023
$23.9M
Characterization of biased airway smooth muscle TAS2R agonists for treating asthmaR01HL155532 · NHLBI · UNIVERSITY OF SOUTH FLORIDA · PI LIGGETT, STEPHEN B · 2021 to 2024
$2.2M
Label-free single molecule detection for basic science and translational medicineR35GM137988 · NIGMS · UNIVERSITY OF ARIZONA · PI SU, JUDITH · 2020 to 2024
$1.8M
Label-free, highly-specific, small molecule detection using microtoroid optical resonatorsR21MH111109 · NIMH · UNIVERSITY OF ARIZONA · PI SU, JUDITH · 2016 to 2017
$396k
NHLBI NIH HHS P01 HL114471NHLBI NIH HHS R01 HL155532NIGMS NIH HHS R35 GM137988NIMH NIH HHS R21 MH111109U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01HL114471U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01HL155532U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R35GM137988U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) R21MH111109
6 · The paper itself

Abstract

G-protein coupled receptors help regulate cellular function and communication, and are targets of small molecule drug discovery efforts. Conventional techniques to probe these interactions require labels and large amounts of receptor to achieve satisfactory sensitivity. Here, we use frequency-locked optical microtoroids for label-free characterization of membrane interactions in vitro at zeptomolar concentrations for the kappa opioid receptor and its native agonist dynorphin A 1-13, as well as big dynorphin (dynorphin A and dynorphin B) using a supported biomimetic membrane. The measured affinity of the agonist dynorphin A 1-13 to the κ-opioid receptor was also measured and found to be 3.1 nM. Radioligand assays revealed a dissociation constant in agreement with this value (1.1 nM). The limit of detection for the κOR/DynA 1-13 was calculated as 180 zM. The binding of Cholera Toxin B-monosialotetrahexosyl ganglioside was also monitored in real-time and an equilibrium dissociation constant of 1.53 nM was found. Our biosensing platform provides a method for highly sensitive real-time characterization of membrane embedded protein binding kinetics that is rapid and label-free, for drug discovery and toxin screening among other applications.

Indexed as

DynorphinsReceptors, Opioid, kappaBiosensing TechniquesCholera ToxinHumansProtein BindingRadioligand AssayCholera ToxinDynorphinsReceptors, Opioid, kappa

Identifiers

PMID39198447
PMCPMC11358326

What OpenQuestion holds

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Registered trials

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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.