Evidence map›Paper›PMID 21368157›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2011

Vertical nanopillars for highly localized fluorescence imaging.

Chong Xie, Lindsey Hanson, Yi Cui, Bianxiao Cui

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Review
  2. Review
  3. Semi-Implantable Bioelectronics.Nano-micro letters · 2022
    Review
  4. Article
  5. High-Aspect-Ratio Nanostructured Surfaces as Biological Metamaterials.Advanced materials (Deerfield Beach, Fla.) · 2020
    Review
  6. Article
  7. Interfacing Cells with Vertical Nanoscale Devices: Applications and Characterization.Annual review of analytical chemistry (Palo Alto, Calif.) · 2018
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Nanotechnology and regenerative therapeutics in plastic surgery: The next frontier.Journal of plastic, reconstructive & aesthetic surgery : JPRAS · 2016
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Synthetic nanoelectronic probes for biological cells and tissues.Annual review of analytical chemistry (Palo Alto, Calif.) · 2013
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Chong XieDepartment of Materials Science and Engineering, Stanford University, Stanford, CA 94305, USA.
Lindsey Hanson
Yi Cui
Bianxiao Cui

Funding

Engineering external forces for manipulating cargo transport in live neuronsDP2NS082125 · NINDS · STANFORD UNIVERSITY · PI CUI, BIANXIAO · 2012 to 2012
$2.4M
Imaging NGF signal transduction in live neuronsR00NS057906 · NINDS · STANFORD UNIVERSITY · PI CUI, BIANXIAO · 2008 to 2010
$852k
Imaging nerve growth factor signal transduction in live neuronsK99NS057906 · NINDS · STANFORD UNIVERSITY · PI CUI, BIANXIAO · 2007 to 2008
$117k
NINDS NIH HHS DP2 NS082125NINDS NIH HHS K99 NS057906NINDS NIH HHS NS057906NINDS NIH HHS R00 NS057906
6 · The paper itself

Abstract

Observing individual molecules in a complex environment by fluorescence microscopy is becoming increasingly important in biological and medical research, for which critical reduction of observation volume is required. Here, we demonstrate the use of vertically aligned silicon dioxide nanopillars to achieve below-the-diffraction-limit observation volume in vitro and inside live cells. With a diameter much smaller than the wavelength of visible light, a transparent silicon dioxide nanopillar embedded in a nontransparent substrate restricts the propagation of light and affords evanescence wave excitation along its vertical surface. This effect creates highly confined illumination volume that selectively excites fluorescence molecules in the vicinity of the nanopillar. We show that this nanopillar illumination can be used for in vitro single-molecule detection at high fluorophore concentrations. In addition, we demonstrate that vertical nanopillars interface tightly with live cells and function as highly localized light sources inside the cell. Furthermore, specific chemical modification of the nanopillar surface makes it possible to locally recruit proteins of interest and simultaneously observe their behavior within the complex, crowded environment of the cell.

Indexed as

NanostructuresMicroscopy, FluorescenceSilicon DioxideSilicon Dioxide

Identifiers

PMID21368157
PMCPMC3054026

What OpenQuestion holds

Textmetadata
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.