Evidence map›Paper›PMID 22624874›Full record

ArticleAnalytical chemistry2012

Selection strategy to generate aptamer pairs that bind to distinct sites on protein targets.

Qiang Gong, Jinpeng Wang, Kareem M Ahmad, Andrew T Csordas, Jiehua Zhou, Jeff Nie, Ron Stewart, James A Thomson, John J Rossi, H Tom Soh

Abstract read
In one paragraph

Article in Analytical chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Updates on Aptamer Research.International journal of molecular sciences · 2019
    Review
  8. Article
  9. Review
  10. Selection of DNA aptamers with two modified bases.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  11. Aptamer-based sandwich-type biosensors.Journal of biological engineering · 2017
    Review
  12. The expanding world of DNA and RNA.Current opinion in chemical biology · 2016
    Review
  13. Article
  14. Methods for Improving Aptamer Binding Affinity.Molecules (Basel, Switzerland) · 2016
    Review
  15. Review
  16. Article
  17. Array-based discovery of aptamer pairs.Analytical chemistry · 2015
    Article
  18. Article
  19. Review
  20. 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

10 authors.

Qiang GongInterdepartmental Program in Biomolecular Science and Engineering, University of California Santa Barbara, Santa Barbara, California 93106, USA.
Jinpeng Wang
Kareem M Ahmad
Andrew T Csordas
Jiehua Zhou
Jeff Nie
Ron Stewart
James A Thomson
John J Rossi
H Tom Soh

Funding

COMBINATORIAL USE OF CCR5 RIBOZYMES WITH ANTI HIV1 RNASR01AI042552 · NIAID · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI ROSSI, JOHN JOSEPH · 1998 to 2019
$7.8M
Midwest Progenitor Cell ConsortiumU01HL099773 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI THOMSON, JAMES ALEXANDER · 2009 to 2015
$7.8M
YEAST SYSTEM FOR DEVELOPING ANTI-HIV-1 RIBOZYMESR01AI029329 · NIAID · LOMA LINDA UNIVERSITY · PI ROSSI, JOHN JOSEPH · 1990 to 2018
$3.9M
QPASS: Quantitative Parallel Aptamer Selection SystemU54DK093467 · NIDDK · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI SMITH, LLOYD M, SOH, HYONGSOK TOM · 2011 to 2013
$3.2M
Strain Specific Detection of Influenza at the Point-of-CareR01EB009764 · NIBIB · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI SOH, HYONGSOK TOM · 2009 to 2012
$1.5M
NHLBI NIH HHS U01 HL099773NIAID NIH HHS R01 AI029329NIAID NIH HHS R01 AI042552NIBIB NIH HHS R01 EB009764NIDDK NIH HHS U54 DK093467
6 · The paper itself

Abstract

Many analytical techniques benefit greatly from the use of affinity reagent pairs, wherein each reagent recognizes a discrete binding site on a target. For example, antibody pairs have been widely used to dramatically increase the specificity of enzyme linked immunosorbent assays (ELISA). Nucleic acid-based aptamers offer many advantageous features relative to protein-based affinity reagents, including well-established chemical synthesis, thermostability, and low production cost. However, the generation of suitable aptamer pairs has posed a significant challenge, and few such pairs have been reported to date. To address this important challenge, we present multivalent aptamer isolation systematic evolution of ligands by exponential enrichment (MAI-SELEX), a technique designed for the efficient selection of aptamer pairs. In contrast to conventional selection methods, our method utilizes two selection modules to generate separate aptamer pools that recognize distinct binding sites on a single target. Using MAI-SELEX, we have isolated two groups of 2'-fluoro-modified RNA aptamers that specifically recognize the αV or β3 subunits of integrin αVβ3. These aptamers exhibit low nanomolar affinities for their targets, with minimal cross-reactivity to other closely related integrin homologues. Moreover, we show that these aptamer pairs do not interfere with each other's binding and effectively detect the target even in complex mixtures such as undiluted serum.

Indexed as

AnimalsAptamers, NucleotideBinding SitesCattleIntegrin alphaVbeta3LigandsProtein SubunitsSELEX Aptamer TechniqueSequence Homology, Amino AcidSubstrate SpecificityAptamers, NucleotideIntegrin alphaVbeta3LigandsProtein Subunits

Identifiers

PMID22624874
PMCPMC3382006

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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.