Evidence map›Paper›PMID 22742968›Full record

ArticleJournal of proteome research2012

High density diffusion-free nanowell arrays.

Bharath R Takulapalli, Ji Qiu, D Mitchell Magee, Peter Kahn, Al Brunner, Kristi Barker, Steven Means, Shane Miersch, Xiaofang Bian, Alex Mendoza and 5 more

Abstract read
In one paragraph

Article in Journal of proteome research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Trial
  2. Article
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  5. Article
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  8. Comparative Microbiomics Analysis of Antimicrobial Antibody Response between Patients with Lung Cancer and Control Subjects with Benign Pulmonary Nodules.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2023
    Article
  9. Article
  10. Article
  11. Identification of anti-Epstein-Barr virus (EBV) antibody signature in EBV-associated gastric carcinoma.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2021
    Article
  12. Review
  13. Article
  14. Review
  15. Multi-platform Approach for Microbial Biomarker Identification UsingFrontiers in cellular and infection microbiology · 2019
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  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

15 authors.

Bharath R TakulapalliBiodesign Institute, Center for Personal Diagnostics, Arizona State University, Tempe, Arizona 85287, United States.
Ji Qiu
D Mitchell Magee
Peter Kahn
Al Brunner
Kristi Barker
Steven Means
Shane Miersch
Xiaofang Bian
Alex Mendoza
Fernanda Festa
Karan Syal
Jin G Park
Joshua LaBaer
Peter Wiktor

Funding

Biomarker Detection Using NAPPA Tumor Antigen ArraysU01CA117374 · NCI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI ANDERSON, KAREN SUE, LABAER, JOSHUA · 2005 to 2015
$6.2M
Piezoelectric Pipetting for High Density Nucleic Acid Programmable Protein ArraysR42RR031446 · NCRR · ENGINEERING ARTS, LLC · PI WIKTOR, PETER J. · 2010 to 2011
$427k
NCI NIH HHS 5U01CA117374NCI NIH HHS U01 CA117374NCRR NIH HHS 5R42RR031446-01NCRR NIH HHS R42 RR031446
6 · The paper itself

Abstract

Proteomics aspires to elucidate the functions of all proteins. Protein microarrays provide an important step by enabling high-throughput studies of displayed proteins. However, many functional assays of proteins include untethered intermediates or products, which could frustrate the use of planar arrays at very high densities because of diffusion to neighboring features. The nucleic acid programmable protein array (NAPPA) is a robust in situ synthesis method for producing functional proteins just-in-time, which includes steps with diffusible intermediates. We determined that diffusion of expressed proteins led to cross-binding at neighboring spots at very high densities with reduced interspot spacing. To address this limitation, we have developed an innovative platform using photolithographically etched discrete silicon nanowells and used NAPPA as a test case. This arrested protein diffusion and cross-binding. We present confined high density protein expression and display, as well as functional protein-protein interactions, in 8000 nanowell arrays. This is the highest density of individual proteins in nanovessels demonstrated on a single slide. We further present proof of principle results on ultrahigh density protein arrays capable of up to 24000 nanowells on a single slide.

Indexed as

Lab-On-A-Chip DevicesDiffusionHumansProtein Array AnalysisProtein BiosynthesisProtein Interaction MappingProteomeProteomicsSiliconProteomeSilicon

Identifiers

PMID22742968
PMCPMC3412896

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.