Evidence map›Paper›PMID 34347442›Full record

ArticleAnalytical chemistry2021

Enhancing the Sensitivity of the Virus BioResistor by Overoxidation: Detecting IgG Antibodies.

Apurva Bhasin, Eric J Choi, Nicholas P Drago, Jason E Garrido, Emily C Sanders, Jihoon Shin, Ilektra Andoni, Dong-Hwan Kim, Lu Fang, Gregory A Weiss and 1 more

Open access · greenAbstract read
In one paragraph

Article in Analytical chemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

1 citing paper in PubMed, 8 citations in OpenAlex.

  1. Review
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

11 authors at 3 institutions in 3 countries.

Apurva BhasinDepartment of Chemistry, University of California, Irvine, Irvine, California 92697, United States.
Eric J ChoiDepartment of Chemistry, University of California, Irvine, Irvine, California 92697, United States.ORCID 0000-0003-3287-1284
Nicholas P DragoDepartment of Chemistry, University of California, Irvine, Irvine, California 92697, United States.ORCID 0000-0002-3790-552X
Jason E GarridoDepartment of Chemistry, University of California, Irvine, Irvine, California 92697, United States.
Emily C SandersDepartment of Chemistry, University of California, Irvine, Irvine, California 92697, United States.ORCID 0000-0003-1043-5772
Jihoon ShinSchool of Chemical Engineering, Sungkyunkwan University, Jangan-gu, Suwon, Gyeonggi-do 16419, South Korea.
Ilektra AndoniDepartment of Chemistry, University of California, Irvine, Irvine, California 92697, United States.
Dong-Hwan KimSchool of Chemical Engineering, Sungkyunkwan University, Jangan-gu, Suwon, Gyeonggi-do 16419, South Korea.ORCID 0000-0002-2753-0955
Lu FangDepartment of Automation, Hangzhou Dianzi University, Xiasha, Hangzhou 310018, China.
Gregory A WeissDepartment of Chemistry, University of California, Irvine, Irvine, California 92697, United States.ORCID 0000-0003-0296-9846
Reginald M PennerDepartment of Chemistry, University of California, Irvine, Irvine, California 92697, United States.ORCID 0000-0003-2831-3028
University of California, Irvine · USSungkyunkwan University · KRHangzhou Dianzi University · CN

Funding

Monitoring Recurrent Bladder Cancer with Electro-Phage BiosensorsR33CA206955 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI WEISS, GREGORY A. · 2016 to 2018
$932k
NCI NIH HHS R33 CA206955
6 · The paper itself

Abstract

The Virus BioResistor (VBR) is a biosensor capable of rapid and sensitive detection of small protein disease markers using a simple dip-and-read modality. For example, the bladder cancer-associated protein DJ-1 (22 kDa) can be detected in human urine within 1.0 min with a limit of detection (LOD) of 10 pM. The VBR uses engineered virus particles as receptors to recognize and selectively bind the protein of interest. These virus particles are entrained in a conductive poly(3,4-ethylenedioxythiophene) or PEDOT channel. The electrical impedance of the channel increases when the target protein is bound by the virus particles. But VBRs exhibit a sensitivity that is inversely related to the molecular weight of the protein target. Thus, large proteins, such as IgG antibodies (150 kDa), can be undetectable even at high concentrations. We demonstrate that the electrochemical overoxidation of the VBR's PEDOT channel increases its electrical impedance, conferring enhanced sensitivity for both small and large proteins. Overoxidation makes possible the detection of two antibodies, undetectable at a normal VBR, with a limit of detection of 40 ng/mL (250 pM), and a dynamic range for quantitation extending to 600 ng/mL.

Indexed as

Biosensing TechniquesBridged Bicyclo Compounds, HeterocyclicHumansImmunoglobulin GLimit of DetectionPolymersBridged Bicyclo Compounds, HeterocyclicImmunoglobulin GPolymers

Identifiers

PMID34347442
PMCPMC9096803
OpenAlexW3189931986

What OpenQuestion holds

Textmetadata
LicenceTDM
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.