Evidence map›Paper›PMID 39671183›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

The C-terminal activating domain promotes pannexin 1 channel opening.

Erik Henze, Jacqueline J Ehrlich, Janice L Robertson, Eric Gelsleichter, Toshimitsu Kawate

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. PANX1 hexamers work but cells prefer heptamers.The Journal of general physiology · 2025
    Article
  7. Article
  8. Pannexin channels in inflammation and tumorigenesis.Frontiers in cell and developmental biology · 2025
    Review
  9. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Erik Henze *Department of Molecular Medicine, Cornell University, Ithaca, NY 14853.
Jacqueline J Ehrlich *Department of Molecular Medicine, Cornell University, Ithaca, NY 14853.ORCID 0000-0002-8761-7198
Janice L Robertson *Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, MO 63110.ORCID 0000-0002-5499-9943
Eric GelsleichterDepartment of Molecular Medicine, Cornell University, Ithaca, NY 14853.ORCID 0000-0002-5970-813X
Toshimitsu KawateDepartment of Molecular Medicine, Cornell University, Ithaca, NY 14853.ORCID 0000-0002-5005-2031

Funding

Driving forces of membrane protein assembly in membranesR01GM120260 · NIGMS · WASHINGTON UNIVERSITY · PI ROBERTSON, JANICE L · 2016 to 2024
$3.4M
Structure and Function of Pannexins: Activation MechanismR01GM114379 · NIGMS · CORNELL UNIVERSITY · PI KAWATE, TOSHIMITSU · 2015 to 2025
$3.1M
Cryo Transmission Electron Microscope for Cryo-EM Sample OptimizationS10OD030470 · OD · CORNELL UNIVERSITY · PI KELLOGG, ELIZABETH · 2021 to 2021
$1.1M
Determinants of amino acid transporter oligomerization in membranesR03NS133680 · NINDS · WASHINGTON UNIVERSITY · PI ROBERTSON, JANICE L · 2023 to 2023
$156k
HHS | NIH (NIH) R01GM114379HHS | NIH (NIH) R01GM120260HHS | NIH (NIH) R03NS133680Margaret and Richard Riney Canine Health Center Research Grants Program N/ANIGMS NIH HHS R01 GM114379NIGMS NIH HHS R01 GM120260NIH HHS S10 OD030470NINDS NIH HHS R03 NS133680
6 · The paper itself

Abstract

Pannexin 1 (Panx1) constitutes a large pore channel responsible for the release of adenosine triphosphate (ATP) from apoptotic cells. Strong evidence indicates that caspase-mediated cleavage of the C-terminus promotes the opening of the Panx1 channel by unplugging the pore. However, this simple pore-plugging mechanism alone cannot account for the observation that a Panx1 construct ending before the caspase cleavage site remains closed. Here, we show that a helical region located immediately before the caspase cleavage site, referred to as the "C-terminal activating domain (CAD)", plays a pivotal role in facilitating Panx1 activation. Electrophysiology and mutagenesis studies uncovered that two conserved leucine residues within the CAD play a pivotal role. Cryoelectron microscopy (Cryo-EM) analysis of the construct ending before reaching the CAD demonstrated that the N terminus extends into an intracellular pocket. In contrast, the construct including the CAD revealed that this domain occupies the intracellular pocket, causing the N terminus to flip upward within the pore. Analysis of electrostatic free energy landscape in the closed conformation indicated that the intracellular side of the ion permeation pore may be occupied by anions like ATP, creating an electrostatic barrier for anions attempting to permeate the pore. When the N terminus flips up, it diminishes the positively charged surface, thereby reducing the drive to accumulate anions inside the pore. This dynamic change in the electrostatic landscape likely contributes to the selection of permeant ions. Collectively, these experiments put forth a mechanism in which C-terminal cleavage liberates the CAD, causing the repositioning of the N terminus to promote Panx1 channel opening.

Indexed as

ConnexinsCryoelectron MicroscopyNerve Tissue ProteinsAdenosine TriphosphateAnimalsHumansIon Channel GatingProtein DomainsAdenosine TriphosphateConnexinsNerve Tissue ProteinsPANX1 protein, humancaspase cleavageelectrostatic barrierlarge pore channelmetabolite release

Identifiers

PMID39671183
PMCPMC11665872

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.