Evidence map›Paper›PMID 26972784›Full record

ArticleMethods (San Diego, Calif.)2016

AFBI assay - Aptamer Fluorescence Binding and Internalization assay for cultured adherent cells.

William H Thiel, Paloma H Giangrande

Open access · greenAbstract read
In one paragraph

Article in Methods (San Diego, Calif.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. A CRISPR View of Biological Mechanisms.Discoveries (Craiova, Romania) · 2016
    Review
  4. Advances in RNA structure determination.Methods (San Diego, Calif.) · 2016
    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

2 authors at 1 institution in 1 country.

William H ThielDepartment of Internal Medicine, University of Iowa, Iowa City, IA 52242, USA; The François M. Abboud Cardiovascular Research Center, University of Iowa, Iowa City, IA 52242, USA. Electronic address: william-thiel@uiowa.edu.
Paloma H GiangrandeDepartment of Internal Medicine, University of Iowa, Iowa City, IA 52242, USA; The François M. Abboud Cardiovascular Research Center, University of Iowa, Iowa City, IA 52242, USA; The Holden Comprehensive Cancer Center, University of Iowa, Iowa City, IA 52242, USA; The Molecular and Cell Biology Program, University of Iowa, Iowa City, IA 52242, USA. Electronic address: paloma-giangrande@uiowa.edu.
University of Iowa · US

Funding

Aptamer-siRNA Chimeras Targeting HER2-Positive Breast CancersR01CA138503 · NCI · UNIVERSITY OF IOWA · PI GIANGRANDE, PALOMA HOBAN · 2009 to 2013
$1.5M
Novel Chimeric RNA Aptamer Technology to Treat Head and Neck CancerR21DE019953 · NIDCR · UNIVERSITY OF IOWA · PI GIANGRANDE, PALOMA HOBAN, KLINGELHUTZ, ALOYSIUS JOHN · 2009 to 2010
$410k
NCI NIH HHS R01 CA138503NIDCR NIH HHS R21 DE019953
6 · The paper itself

Abstract

The SELEX (Systematic Evolution of Ligands by Exponential Enrichment) process allows for the enrichment of DNA or RNA aptamers from a complex nucleic acid library that are specific for a target molecule. The SELEX process has been adapted from identifying aptamers in vitro using recombinant target protein to cell-based methodologies (Cell-SELEX), where the targets are expressed on the surface of cells. One major advantage of Cell-SELEX is that the target molecules are maintained in a native confirmation. Additionally, Cell-SELEX may be used to discover novel therapeutic biomarkers by performing selections on diseased versus healthy cells. However, a caveat to Cell-SELEX is that testing of single aptamers identified in the selection is laborious, time-consuming, and expensive. The most frequently used methods to screen for aptamer binding and internalization on cells are flow cytometry and quantitative PCR (qPCR). While flow cytometry can directly assess binding of a fluorescently-labeled aptamer to a target, it requires significant starting material and is not easily scalable. qPCR-based approaches are highly sensitive but have non-negligible experiment-to-experiment variability due to the number of sample processing steps. Herein we describe a cell-based aptamer fluorescence binding and internalization (AFBI) assay. This assay requires minimal reagents and has few experimental steps/manipulations, thereby allowing for rapid screening of many aptamers and conditions simultaneously and direct quantitation of aptamer binding and internalization.

Indexed as

Aptamers, NucleotideCell AdhesionCells, CulturedHumansSELEX Aptamer TechniqueSpectrometry, FluorescenceStaining and LabelingAptamers, NucleotideAptamerCell-SELEXFluorescenceMicroplate readerSELEX

Identifiers

PMID26972784
PMCPMC4921262
OpenAlexW2294914325

What OpenQuestion holds

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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 OpenQuestion graph.