Evidence map›Paper›PMID 22458258›Full record

ArticleLangmuir : the ACS journal of surfaces and colloids2012

On-chip synthesis of RNA aptamer microarrays for multiplexed protein biosensing with SPR imaging measurements.

Yulin Chen, Kohei Nakamoto, Osamu Niwa, Robert M Corn

Abstract read
In one paragraph

Article in Langmuir : the ACS journal of surfaces and colloids, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Review
  3. Molecular Diagnosis and Cancer Prognosis-A Concise Review.Diagnostics (Basel, Switzerland) · 2023
    Review
  4. Review
  5. Review
  6. Spotting, Transcription andComputational and structural biotechnology journal · 2019
    Review
  7. High-Density RNA Microarrays Synthesized In Situ by Photolithography.Angewandte Chemie (International ed. in English) · 2018
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Surface Enzyme Chemistries for Ultrasensitive Microarray Biosensing with SPR Imaging.Langmuir : the ACS journal of surfaces and colloids · 2015
    Article
  13. Review
  14. Aptamer Microarrays-Current Status and Future Prospects.Microarrays (Basel, Switzerland) · 2015
    Review
  15. Silica nanowire arrays for diffraction-based bioaffinity sensing.Chemistry (Weinheim an der Bergstrasse, Germany) · 2014
    Article
  16. Article
  17. Article
  18. Article
  19. 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

4 authors at 2 institutions in 2 countries.

Yulin ChenDepartment of Chemistry, University of California-Irvine, Irvine, California 92697, USA.
Kohei Nakamoto
Osamu Niwa
Robert M Corn
University of California, Irvine · USUniversity of Tsukuba · JP

Funding

SPR IMAGING STUDIES OF PROTEIN/DNA INTERACTIONSR01GM059622 · NIGMS · UNIVERSITY OF WISCONSIN MADISON · PI CORN, ROBERT M · 1999 to 2018
$5.1M
NIGMS NIH HHS 2R01 GM059622NIGMS NIH HHS R01 GM059622
6 · The paper itself

Abstract

Microarrays of RNA aptamers are fabricated in a one-step, multiplexed enzymatic synthesis on gold thin films in a microfluidic format and then employed in the detection of protein biomarkers with surface plasmon resonance imaging (SPRI) measurements. Single-stranded RNA (ssRNA) oligonucleotides are transcribed on-chip from double-stranded DNA (dsDNA) templates attached to microarray elements (denoted as generator elements) by the surface transcription reaction of T7 RNA polymerase. As they are synthesized, the ssRNA oligonucleotides diffuse in the microfluidic channel and are quickly captured by hybridization adsorption onto adjacent single-stranded DNA (ssDNA) microarray elements (denoted as detector elements) that contain a sequence complementary to 5'-end of the ssRNA. The RNA aptamers attached to these detector elements are subsequently used in SPRI measurements for the bioaffinity detection of protein biomarkers. The microfluidic generator-detector element format permits the simultaneous fabrication of multiple ssRNA oligonucleotides with different capture sequences that can hybridize simultaneously to distinct detector elements and thus create a multiplexed aptamer microarray. In an initial set of demonstration experiments, SPRI measurements are used to monitor the bioaffinity adsorption of human thrombin (hTh) and vascular endothelial growth factor (VEGF) proteins onto RNA aptamer microarrays fabricated in situ with this on-chip RNA polymerase synthesis methodology. Additional SPRI measurements of the hydrolysis and desorption of the surface-bound ssRNA aptamers with a surface RNase H are used to verify the capture of ssRNA with RNA-DNA surface hybridization onto the detector elements. The on-chip RNA synthesis described here is an elegant, one-step multiplexed methodology for the rapid and contamination-free fabrication of RNA aptamer microarrays for protein biosensing with SPRI.

Indexed as

AdsorptionAptamers, NucleotideBiomarkersBiosensing TechniquesDNADNA-Directed RNA PolymerasesGoldHumansHydrolysisMicrofluidic Analytical TechniquesNucleic Acid HybridizationOligonucleotide Array Sequence AnalysisRibonuclease HSurface Plasmon ResonanceThrombinVascular Endothelial Growth Factor AAptamers, Nucleotidebacteriophage T7 RNA polymeraseBiomarkersDNADNA-Directed RNA PolymerasesGoldRibonuclease HThrombinVascular Endothelial Growth Factor AVEGFA protein, humanViral Proteins

Identifiers

PMID22458258
PMCPMC3368080
OpenAlexW2083454689

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.