Evidence map›Paper›PMID 27686335›Full record

ArticleAnalytical chemistry2016

A Stimuli-Responsive, Binary Reagent System for Rapid Isolation of Protein Biomarkers.

Barrett J Nehilla, John J Hill, Selvi Srinivasan, Yen-Chi Chen, Thomas H Schulte, Patrick S Stayton, James J Lai

Open access · greenAbstract read
In one paragraph

Article in Analytical chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

6 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Exosome Processing and Characterization Approaches for Research and Technology Development.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    Review
  5. Review
  6. Article
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

7 authors at 1 institution in 1 country.

Barrett J NehillaDepartment of Bioengineering, University of Washington , Seattle, Washington 98195, United States.
John J HillDepartment of Bioengineering, University of Washington , Seattle, Washington 98195, United States.
Selvi SrinivasanDepartment of Bioengineering, University of Washington , Seattle, Washington 98195, United States.
Yen-Chi ChenDepartment of Bioengineering, University of Washington , Seattle, Washington 98195, United States.
Thomas H SchulteDepartment of Bioengineering, University of Washington , Seattle, Washington 98195, United States.
Patrick S StaytonDepartment of Bioengineering, University of Washington , Seattle, Washington 98195, United States.
James J LaiDepartment of Bioengineering, University of Washington , Seattle, Washington 98195, United States.
University of Washington · US

Funding

Smart Polymer Reagents for Sensitivity and Speed-enhanced Clinical DiagnosticsR44GM100558 · NIGMS · NEXGENIA, INC. · PI NEHILLA, BARRETT J · 2013 to 2014
$1.1M
Biospecimen preparation technologies to enable high throughput and highly sensitiR21CA174581 · NCI · UNIVERSITY OF WASHINGTON · PI LAI, JAMES · 2013 to 2015
$692k
Smart Polymer Reagents for Sensitivity and Speed-enhanced Clinical DiagnosticsR43GM100558 · NIGMS · NEXGENIA, INC. · PI SCHULTE, THOMAS · 2012 to 2012
$196k
NCI NIH HHS R21 CA174581NIGMS NIH HHS R43 GM100558NIGMS NIH HHS R44 GM100558
6 · The paper itself

Abstract

Magnetic microbeads exhibit rapid separation characteristics and are widely employed for biomolecule and cell isolations in research laboratories, clinical diagnostics assays, and cell therapy manufacturing. However, micrometer particle diameters compromise biomarker recognition, which leads to long incubation times and significant reagent demands. Here, a stimuli-responsive binary reagent system is presented that combines the nanoscale benefits of efficient biomarker recognition and the microscale benefits of rapid magnetic separation. This system comprises magnetic nanoparticles and polymer-antibody (Ab) conjugates that transition from hydrophilic nanoscale reagents to microscale aggregates in response to temperature stimuli. The binary reagent system was benchmarked against Ab-labeled Dynabeads in terms of biomarker isolation kinetics, assay speed, and reagent needs. Surface plasmon resonance (SPR) measurements showed that polymer conjugation did not significantly alter the Ab's binding affinity or kinetics. ELISA analysis showed that the unconjugated Ab, polymer-Ab conjugates, and Ab-labeled Dynabeads exhibited similar equilibrium dissociation constants (K

Indexed as

BiomarkersEnzyme-Linked Immunosorbent AssayHIVHIV Core Protein p24HIV InfectionsHumansHydrophobic and Hydrophilic InteractionsImmunoconjugatesIndicators and ReagentsMagnetite NanoparticlesPolymersProtein MultimerizationSurface Plasmon ResonanceTemperatureBiomarkersHIV Core Protein p24ImmunoconjugatesIndicators and ReagentsMagnetite NanoparticlesPolymers

Identifiers

PMID27686335
PMCPMC6750004
OpenAlexW2526627378

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.