Evidence map›Paper›PMID 11717428›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2001

High refractive index substrates for fluorescence microscopy of biological interfaces with high z contrast.

C M Ajo-Franklin, L Kam, S G Boxer

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Engineering lipid bilayer membranes for protein studies.International journal of molecular sciences · 2013
    Review
  4. Article
  5. DNA-tethered membranes formed by giant vesicle rupture.Journal of structural biology · 2009
    Article
  6. Review
  7. Article
  8. 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

3 authors.

C M Ajo-FranklinDepartment of Chemistry, Stanford University, Stanford, CA 94305-5080, USA.
L Kam
S G Boxer

Funding

INSTITUTIONAL TRAINING GRANT IN GENOME SCIENCET32HG000044 · NHGRI · STANFORD UNIVERSITY · PI MICHAEL P. SNYDER · 1995 to 2026
$32.2M
COMPUTATIONAL METHODS FOR PROTEOMIC ANALYSISK22HG000044 · NHGRI · UNIVERSITY OF UTAH · PI GIDDINGS, MORGAN CORINNE · 2000 to 2005
$1.3M
CELL ADHESION ON PROTEIN-MICROPATTERNED LIPID BILAYERSF32GM020878 · NIGMS · STANFORD UNIVERSITY · PI KAM, LANCE C · 2001 to 2003
$66k
NHGRI NIH HHS HG00044NHGRI NIH HHS K22 HG000044NHGRI NIH HHS T32 HG000044NIGMS NIH HHS F32 GM020878NIGMS NIH HHS GM20878
6 · The paper itself

Abstract

Total internal reflection fluorescence microscopy is widely used to confine the excitation of a complex fluorescent sample very close to the material on which it is supported. By working with high refractive index solid supports, it is possible to confine even further the evanescent field, and by varying the angle of incidence, to obtain quantitative information on the distance of the fluorescent object from the surface. We report the fabrication of hybrid surfaces consisting of nm layers of SiO(2) on lithium niobate (LiNbO(3), n = 2.3). Supported lipid bilayer membranes can be assembled and patterned on these hybrid surfaces as on conventional glass. By varying the angle of incidence of the excitation light, we are able to obtain fluorescent contrast between 40-nm fluorescent beads tethered to a supported bilayer and fluorescently labeled protein printed on the surface, which differ in vertical position by only tens of nm. Preliminary experiments that test theoretical models for the fluorescence-collection factor near a high refractive index surface are presented, and this factor is incorporated into a semiquantitative model used to predict the contrast of the 40-nm bead/protein system. These results demonstrate that it should be possible to profile the vertical location of fluorophores on the nm distance scale in real time, opening the possibility of many experiments at the interface between supported membranes and living cells. Improvements in materials and optical techniques are outlined.

Indexed as

Lipid BilayersNiobiumOxidesSilicon DioxideContrast SensitivityFluorescent DyesImage EnhancementMathematical ComputingMicroscopy, FluorescencePhosphatidylcholinesPhosphatidylethanolaminesXanthenes1,2-dipalmitoyl-3-phosphatidylethanolamineFluorescent DyesLipid Bilayerslithium niobateNiobiumOxidesPhosphatidylcholinesPhosphatidylethanolaminesSilicon DioxideTexas redXanthenes

Identifiers

PMID11717428
PMCPMC61094

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.