Evidence map›Paper›PMID 35075142›Full record

ArticleScientific reports2022

Quantum optical immunoassay: upconversion nanoparticle-based neutralizing assay for COVID-19.

Navid Rajil, Shahriar Esmaeili, Benjamin W Neuman, Reed Nessler, Hung-Jen Wu, Zhenhuan Yi, Robert W Brick, Alexei V Sokolov, Philip R Hemmer, Marlan O Scully

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-weighted citation impact, top 21% of its field
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

5 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  4. Review
  5. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 2 countries.

Navid RajilInstitute for Quantum Science and Engineering, Texas A&M University, College Station, TX, 77843, USA.
Shahriar EsmaeiliInstitute for Quantum Science and Engineering, Texas A&M University, College Station, TX, 77843, USA.
Benjamin W NeumanInstitute for Quantum Science and Engineering, Texas A&M University, College Station, TX, 77843, USA.
Reed NesslerInstitute for Quantum Science and Engineering, Texas A&M University, College Station, TX, 77843, USA.
Hung-Jen WuDepartment of Chemical Engineering, Texas A&M University, College Station, TX, 77843, USA.ORCID 0000-0003-3082-7431
Zhenhuan YiInstitute for Quantum Science and Engineering, Texas A&M University, College Station, TX, 77843, USA.
Robert W BrickInstitute for Quantum Science and Engineering, Texas A&M University, College Station, TX, 77843, USA.
Alexei V SokolovInstitute for Quantum Science and Engineering, Texas A&M University, College Station, TX, 77843, USA.
Philip R HemmerInstitute for Quantum Science and Engineering, Texas A&M University, College Station, TX, 77843, USA.
Marlan O ScullyInstitute for Quantum Science and Engineering, Texas A&M University, College Station, TX, 77843, USA. scully@tamu.edu.
Texas A&M University · USBaylor University · USKazan Scientific Center · RUTexas A&M University System · US

Funding

Design of hetero-multivalent targeted liposome for combating intracellular Mycobacterium tuberculosisR21AI149383 · NIAID · TEXAS ENGINEERING EXPERIMENT STATION · PI CIRILLO, JEFFREY D., WU, HUNG-JEN · 2020 to 2021
$416k
Study the interaction between Lipopolysaccharide-Binding Protein and Immune Cell MembranesR03AI139650 · NIAID · TEXAS ENGINEERING EXPERIMENT STATION · PI JAYARAMAN, ARUL, WU, HUNG-JEN · 2019 to 2020
$149k
National Science Foundation (NSF) ECCS-2032589National Science Foundation (NSF) PHY-1820930National Science Foundation (NSF) PHY-2013771NIAID NIH HHS R03 AI139650NIAID NIH HHS R21 AI149383United States Department of Defense | United States Air Force | AFMC | Air Force Office of Scientific Research (AF Office of Scientific Research) FA9550-20-1-0366 DEFUnited States Department of Defense | United States Navy | Office of Naval Research (ONR) N00014-20-1-2184
6 · The paper itself

Abstract

In a viral pandemic, a few important tests are required for successful containment of the virus and reduction in severity of the infection. Among those tests, a test for the neutralizing ability of an antibody is crucial for assessment of population immunity gained through vaccination, and to test therapeutic value of antibodies made to counter the infections. Here, we report a sensitive technique to detect the relative neutralizing strength of various antibodies against the SARS-CoV-2 virus. We used bright, photostable, background-free, fluorescent upconversion nanoparticles conjugated with SARS-CoV-2 receptor binding domain as a phantom virion. A glass bottom plate coated with angiotensin-converting enzyme 2 (ACE-2) protein imitates the target cells. When no neutralizing IgG antibody was present in the sample, the particles would bind to the ACE-2 with high affinity. In contrast, a neutralizing antibody can prevent particle attachment to the ACE-2-coated substrate. A prototype system consisting of a custom-made confocal microscope was used to quantify particle attachment to the substrate. The sensitivity of this assay can reach 4.0 ng/ml and the dynamic range is from 1.0 ng/ml to 3.2 [Formula: see text]g/ml. This is to be compared to 19 ng/ml sensitivity of commercially available kits.

Indexed as

COVID-19 Serological TestingAngiotensin-Converting Enzyme 2Antibodies, NeutralizingAntibodies, ViralCOVID-19FluoroimmunoassayHumansNanoparticlesNeutralization TestsSARS-CoV-2ACE2 protein, humanAngiotensin-Converting Enzyme 2Antibodies, NeutralizingAntibodies, Viral

Identifiers

PMID35075142
PMCPMC8786937
OpenAlexW3206116745

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.