Evidence map›Paper›PMID 22728885›Full record

ArticleLab on a chip2012

Electro-optical BLM chips enabling dynamic imaging of ordered lipid domains.

Chenren Shao, Eric L Kendall, Don L DeVoe

Abstract read
In one paragraph

Article in Lab on a chip, 2012. 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.

Chenren ShaoDepartment of Mechanical Engineering, University of Maryland, College Park, MD 20742, USA.
Eric L Kendall
Don L DeVoe

Funding

Microfluidic Platform for Probing Ceramide ChannelsR21EB009485 · NIBIB · UNIV OF MARYLAND, COLLEGE PARK · PI DEVOE, DON L · 2009 to 2010
$399k
Single Molecule Mass Spectrometry in a Microfluidic Nanopore ChipR21EB011750 · NIBIB · UNIV OF MARYLAND, COLLEGE PARK · PI DEVOE, DON L · 2010 to 2010
$214k
NIBIB NIH HHS R21 EB009485NIBIB NIH HHS R21EB009485NIBIB NIH HHS R21 EB011750NIBIB NIH HHS R21EB011750
6 · The paper itself

Abstract

Studies of lipid rafts, ordered microdomains of sphingolipids and cholesterol within cell membranes, are essential in probing the relationships between membrane organization and cellular function. While in vitro studies of lipid phase separation are commonly performed using spherical vesicles as model membranes, the utility of these models is limited by a number of factors. Here we present a microfluidic device that supports simultaneous electrical measurements and confocal imaging of on-chip bilayer lipid membranes (BLMs), enabling real-time multi-domain imaging of membrane organization. The chips further support closed microfluidic access to both sides of the membrane, allowing the membrane boundary conditions to be rapidly changed and providing a mechanism for dynamically adjusting membrane curvature through application of a transmembrane pressure gradient. Here we demonstrate the platform through the study of dynamic generation and dissolution of ordered lipid domains as membrane components are transported to and from the supporting annulus containing solvated lipids and cholesterol.

Indexed as

1,2-DipalmitoylphosphatidylcholineCholesterolLipid BilayersMembrane MicrodomainsMicrofluidic Analytical TechniquesMicroscopy, ConfocalPhosphatidylcholinesPressureSphingolipidsUnilamellar Liposomes1,2-Dipalmitoylphosphatidylcholine1-palmitoyl-2-oleoylphosphatidylcholineCholesterolLipid BilayersPhosphatidylcholinesSphingolipidsUnilamellar Liposomes

Identifiers

PMID22728885
PMCPMC3411933

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.