Evidence map›Paper›PMID 27981836›Full record

ArticleAnalytical chemistry2017

Enhanced Temporal Resolution with Ion Channel-Functionalized Sensors Using a Conductance-Based Measurement Protocol.

Mark T Agasid, Troy J Comi, S Scott Saavedra, Craig A Aspinwall

Abstract read
In one paragraph

Article in Analytical chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Membrane protein-based biosensors.Journal of the Royal Society, Interface · 2018
    Review
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

4 authors.

Mark T AgasidDepartment of Chemistry and Biochemistry, ‡BIO5 Institute, and §Department of Biomedical Engineering, University of Arizona , Tucson, Arizona 85721, United States.
Troy J ComiDepartment of Chemistry and Biochemistry, ‡BIO5 Institute, and §Department of Biomedical Engineering, University of Arizona , Tucson, Arizona 85721, United States.
S Scott SaavedraDepartment of Chemistry and Biochemistry, ‡BIO5 Institute, and §Department of Biomedical Engineering, University of Arizona , Tucson, Arizona 85721, United States.ORCID 0000-0002-9946-2664
Craig A AspinwallDepartment of Chemistry and Biochemistry, ‡BIO5 Institute, and §Department of Biomedical Engineering, University of Arizona , Tucson, Arizona 85721, United States.ORCID 0000-0002-4359-5812

Funding

Sniffer Biosensors Based on Ion Channel-GPCR Chimeras and Polylipid MembranesR01EB007047 · NIBIB · UNIVERSITY OF ARIZONA · PI ASPINWALL, CRAIG A, SAAVEDRA, STEVEN SCOTT · 2006 to 2015
$3.5M
NIBIB NIH HHS R01 EB007047
6 · The paper itself

Abstract

The binding of a target analyte to an ion channel (IC), which is readily detected electrochemically in a label-free manner with single-molecule selectivity and specificity, has generated widespread interest in using natural and engineered ICs as transducers in biosensing platforms. To date, the majority of developments in IC-functionalized sensing have focused on IC selectivity or sensitivity or development of suitable membrane environments and aperture geometries. Comparatively little work has addressed analytical performance criteria, particularly criteria required for temporal measurements of dynamic processes. We report a measurement protocol suitable for rapid, time-resolved monitoring (≤30 ms) of IC-modulated membrane conductance. Key features of this protocol include the reduction of membrane area and the use of small voltage steps (10 mV) and short duration voltage pulses (10 ms), which have the net effect of reducing the capacitive charging and decreasing the time required to achieve steady state currents. Application of a conductance protocol employing three sequential, 10 ms voltage steps (-10 mV, -20 mV, -30 mV) in an alternating, pyramid-like arrangement enabled sampling of membrane conductance every 30 ms. Using this protocol, dynamic IC measurements on black lipid membranes (BLMs) functionalized with gramicidin A were conducted using a fast perfusion system. BLM conductance decreased by 76 ± 7.5% within 30 ms of switching from solutions containing 0 to 1 M Ca

Indexed as

Electric ConductivityBiosensing TechniquesEquipment DesignGramicidinImmobilized ProteinsMembrane LipidsMembranes, ArtificialTransducersGramicidinImmobilized ProteinsMembrane LipidsMembranes, Artificial

Identifiers

PMID27981836
PMCPMC5862562

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.