Evidence map›Paper›PMID 18314938›Full record

ArticleBioconjugate chemistry2008

Light-guided surface engineering for biomedical applications.

Ashwath Jayagopal, Gregory P Stone, Frederick R Haselton

Abstract read
In one paragraph

Article in Bioconjugate chemistry, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Ashwath JayagopalDepartment of Biomedical Engineering, Vanderbilt University, 5932 Stevenson Center, Nashville, TN 37232, USA.
Gregory P Stone
Frederick R Haselton

Funding

Training in Vision ResearchT32EY007135 · NEI · VANDERBILT UNIVERSITY · PI GEOFFREY F WOODMAN · 1994 to 2026
$5.8M
Lagrangian detection of biomolecular interactionsR21EB003516 · NIBIB · VANDERBILT UNIVERSITY · PI HASELTON, FREDERICK R · 2004 to 2005
$415k
NEI NIH HHS T32 EY007135NEI NIH HHS T32EY07135NIBIB NIH HHS EB003516NIBIB NIH HHS R21 EB003516
6 · The paper itself

Abstract

Free radical species generated through fluorescence photobleaching have been reported to effectively couple a water-soluble species to surfaces containing electron-rich sites . In this report, we expand upon this strategy to control the patterned attachment of antibodies and peptides to surfaces for biosensing and tissue engineering applications. In the first application, we compare hydrophobic attachment and photobleaching methods to immobilize FITC-labeled anti-M13K07 bacteriophage antibodies to the SiO2 layer of a differential capacitive biosensor and to the polyester filament of a feedback-controlled filament array. On both surfaces, antibody attachment and function were superior to the previously employed hydrophobic attachment. Furthermore, a laser scanning confocal microscope could be used for automated, software-guided photoattachment chemistry. In a second application, the cell-adhesion peptide RGDS was site-specifically photocoupled to glass coated with fluorescein-conjugated poly(ethylene glycol). RGDS attachment and bioactivity were characterized by a fibroblast adhesion assay. Cell adhesion was limited to sites of RGDS photocoupling. These examples illustrate that fluorophore-based photopatterning can be achieved by both solution-phase fluorophores or surface-adhered fluorophores. The coupling preserves the bioactivity of the patterned species, is amenable to a variety of surfaces, and is readily accessible to laboratories with fluorescence imaging equipment. The flexibility offered by visible light patterning will likely have many useful applications in bioscreening and tissue engineering where the controlled placement of biomolecules and cells is critical, and should be considered as an alternative to chemical coupling methods.

Indexed as

Biosensing TechniquesPhotobleaching3T3 CellsAnimalsAntibodies, MonoclonalBacteriophage M13Cell AdhesionCross-Linking ReagentsFluorescein-5-isothiocyanateFluorescent DyesGlassImmunoglobulin ELightMaleimidesMicePhotochemistryAntibodies, MonoclonalCross-Linking ReagentsFluorescein-5-isothiocyanateFluorescent DyesImmunoglobulin EMaleimidesPolylysine

Identifiers

PMID18314938
PMCPMC2853796

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.