Evidence map›Paper›PMID 34319232›Full record

ArticleeLife2021

Structure and analysis of nanobody binding to the human ASIC1a ion channel.

Yangyu Wu, Zhuyuan Chen, Fred J Sigworth, Cecilia M Canessa

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Antigen-Detected NMR for Minimal Epitope Engineering and Structure-Guided Selection of a NaAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. Conformational plasticity of human acid-sensing ion channel 1a.Nature structural & molecular biology · 2026
    Article
  3. Article
  4. Review
  5. Modulating ion channels with nanobodies.Synthetic and systems biotechnology · 2025
    Review
  6. Review
  7. Review
  8. Epithelial NaComprehensive Physiology · 2024
    Review
  9. Photomodulation of the ASIC1a acidic pocket destabilizes the open state.Protein science : a publication of the Protein Society · 2023
    Article
  10. Nanobodies: Robust miniprotein binders in biomedicine.Advanced drug delivery reviews · 2023
    Review
  11. AFTM: a database of transmembrane regions in the human proteome predicted by AlphaFold.Database : the journal of biological databases and curation · 2023
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Development of a universal nanobody-binding Fab module for fiducial-assisted cryo-EM studies of membrane proteins.Proceedings of the National Academy of Sciences of the United States of America · 2021
    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

4 authors at 2 institutions in 2 countries.

Yangyu WuBasic Sciences Department, Tsinghua University School of Medicine, Beijing, China.ORCID 0000-0001-8064-6132
Zhuyuan ChenBasic Sciences Department, Tsinghua University School of Medicine, Beijing, China.
Fred J SigworthCellular and Molecular Physiology, Yale University School of Medicine, New Haven, United States.ORCID 0000-0002-7178-8494
Cecilia M CanessaBasic Sciences Department, Tsinghua University School of Medicine, Beijing, China.ORCID 0000-0001-7316-5082
Tsinghua University · CNYale University · US

Funding

FLUCTUATIONS IN IONIC CURRENT THROUGH MEMBRANE CHANNELSR01NS021501 · NINDS · YALE UNIVERSITY · PI SIGWORTH, FREDERICK J · 1985 to 2024
$10.9M
NINDS NIH HHS R01 NS021501
6 · The paper itself

Abstract

ASIC1a is a proton-gated sodium channel involved in modulation of pain, fear, addiction, and ischemia-induced neuronal injury. We report isolation and characterization of alpaca-derived nanobodies (Nbs) that specifically target human ASIC1a. Cryo-electron microscopy of the human ASIC1a channel at pH 7.4 in complex with one of these, Nb.C1, yielded a structure at 2.9 Å resolution. It is revealed that Nb.C1 binds to a site overlapping with that of the Texas coral snake toxin (MitTx1) and the black mamba venom Mambalgin-1; however, the Nb.C1-binding site does not overlap with that of the inhibitory tarantula toxin psalmotoxin-1 (PcTx1). Fusion of Nb.C1 with PcTx1 in a single polypeptide markedly enhances the potency of PcTx1, whereas competition of Nb.C1 and MitTx1 for binding reduces channel activation by the toxin. Thus, Nb.C1 is a molecular tool for biochemical and structural studies of hASIC1a; a potential antidote to the pain-inducing component of coral snake bite; and a candidate to potentiate PcTx1-mediated inhibition of hASIC1a in vivo for therapeutic applications.

Indexed as

Acid Sensing Ion ChannelsAnimalsCamelids, New WorldCryoelectron MicroscopyProtein BindingSingle-Domain AntibodiesAcid Sensing Ion ChannelsASIC1 protein, humanSingle-Domain AntibodiesASIC1cryo-electron microscopyMitTx antagonismmolecular biophysicsnanobodyPctx1 potentiationstructural biology

Identifiers

PMID34319232
PMCPMC8318589
OpenAlexW3187032976

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.