Evidence map›Paper›PMID 28202723›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Mapping of voltage sensor positions in resting and inactivated mammalian sodium channels by LRET.

Tomoya Kubota, Thomas Durek, Bobo Dang, Rocio K Finol-Urdaneta, David J Craik, Stephen B H Kent, Robert J French, Francisco Bezanilla, Ana M Correa

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

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  13. Novel protein science enabled by total chemical synthesis.Protein science : a publication of the Protein Society · 2019
    Review
  14. Review
  15. Article
  16. Article
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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

9 authors.

Tomoya KubotaDepartment of Biochemistry and Molecular Biology, The University of Chicago, Chicago, IL 60637.
Thomas DurekInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia.
Bobo DangDepartment of Biochemistry and Molecular Biology, The University of Chicago, Chicago, IL 60637.
Rocio K Finol-UrdanetaDepartment of Physiology and Pharmacology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada, T2N 4N1.
David J CraikInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia.
Stephen B H KentDepartment of Biochemistry and Molecular Biology, The University of Chicago, Chicago, IL 60637.
Robert J FrenchDepartment of Physiology and Pharmacology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada, T2N 4N1; nanicorrea@uchicago.edu french@ucalgary.ca fbezanilla@uchicago.edu.
Francisco BezanillaDepartment of Biochemistry and Molecular Biology, The University of Chicago, Chicago, IL 60637; nanicorrea@uchicago.edu french@ucalgary.ca fbezanilla@uchicago.edu.
Ana M CorreaDepartment of Biochemistry and Molecular Biology, The University of Chicago, Chicago, IL 60637; nanicorrea@uchicago.edu french@ucalgary.ca fbezanilla@uchicago.edu.

Funding

Synthetic Antigen Binder CoreU54GM087519 · NIGMS · UNIVERSITY OF CHICAGO · PI JAVITCH, JONATHAN A · 2010 to 2017
$31.9M
The Electrophysiological Studies of Voltage Gated ChannelsR01GM030376 · NIGMS · UNIVERSITY OF CHICAGO · PI BEZANILLA, FRANCISCO J · 1985 to 2025
$9.1M
ELECTROPHYSIOLOGICAL STUDIES OF VOLTAGE GATED CHANNELSR37GM030376 · NIGMS · UNIVERSITY OF CHICAGO · PI BEZANILLA, FRANCISCO J · 1999 to 2008
$3.7M
Voltage-Gating in Bacterial Ion ChannelsR01GM068044 · NIGMS · UNIVERSITY OF CHICAGO · PI CORREA, ANA M · 2004 to 2010
$1.8M
CIHR MOP-10053NIGMS NIH HHS R01 GM030376NIGMS NIH HHS R01 GM068044NIGMS NIH HHS R37 GM030376NIGMS NIH HHS U54 GM087519
6 · The paper itself

Abstract

Voltage-gated sodium channels (Navs) play crucial roles in excitable cells. Although vertebrate Nav function has been extensively studied, the detailed structural basis for voltage-dependent gating mechanisms remain obscure. We have assessed the structural changes of the Nav voltage sensor domain using lanthanide-based resonance energy transfer (LRET) between the rat skeletal muscle voltage-gated sodium channel (Nav1.4) and fluorescently labeled Nav1.4-targeting toxins. We generated donor constructs with genetically encoded lanthanide-binding tags (LBTs) inserted at the extracellular end of the S4 segment of each domain (with a single LBT per construct). Three different Bodipy-labeled, Nav1.4-targeting toxins were synthesized as acceptors: β-scorpion toxin (Ts1)-Bodipy, KIIIA-Bodipy, and GIIIA-Bodipy analogs. Functional Nav-LBT channels expressed in

Indexed as

AnimalsBinding SitesBoron CompoundsEnergy TransferKineticsLanthanoid Series ElementsMembrane PotentialsMuscle ProteinsMuscle, SkeletalOocytesPatch-Clamp TechniquesRatsScorpion VenomsSodium ChannelsVoltage-Gated Sodium ChannelsXenopus4,4-difluoro-4-bora-3a,4a-diaza-s-indaceneBoron CompoundsLanthanoid Series ElementsMuscle ProteinsScn4a protein, ratScorpion VenomsSodium ChannelsVoltage-Gated Sodium Channelsrelaxed stateslow inactivationvoltage gatingβ-scorpion toxinμ-conotoxin

Identifiers

PMID28202723
PMCPMC5347571

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.