Evidence map›Paper›PMID 35931110›Full record

ReviewJournal of molecular biology2023

Complexin Membrane Interactions: Implications for Synapse Evolution and Function.

Justine A Lottermoser, Jeremy S Dittman

Open access · greenAbstract readReview
In one paragraph

Review in Journal of molecular biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Exploring Intrinsic Disorder in Human Synucleins and Associated Proteins.International journal of molecular sciences · 2024
    Article
  6. Mechanisms of SNARE proteins in membrane fusion.Nature reviews. Molecular cell biology · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. SNARE Proteins in Synaptic Vesicle Fusion.Advances in neurobiology · 2023
    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

2 authors at 2 institutions in 1 country.

Justine A LottermoserDepartment of Biochemistry, Weill Cornell Medicine, New York, NY, United States.
Jeremy S DittmanDepartment of Biochemistry, Weill Cornell Medicine, New York, NY, United States. Electronic address: jed2019@med.cornell.edu.
Cornell University · USWeill Cornell Medicine · US

Funding

Analysis of Synaptic Protein DynamicsR01NS116747 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI Jeremy Samuel Dittman · 2020 to 2026
$2.6M
Elucidating the Complexin C-terminal Domain Mechanism in Neurotransmission RegulationF31NS127534 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI LOTTERMOSER, JUSTINE · 2022 to 2023
$76k
NINDS NIH HHS F31 NS127534NINDS NIH HHS R01 NS116747
6 · The paper itself

Abstract

The molecules and mechanisms behind chemical synaptic transmission have been explored for decades. For several of the core proteins involved in synaptic vesicle fusion, we now have a reasonably detailed grasp of their biochemical, structural, and functional properties. Complexin is one of the key synaptic proteins for which a simple mechanistic understanding is still lacking. Living up to its name, this small protein has been associated with a variety of roles differing between synapses and between species, but little consensus has been reached on its fundamental modes of action. Much attention has been paid to its deeply conserved SNARE-binding properties, while membrane-binding features of complexin and their functional significance have yet to be explored to the same degree. In this review, we summarize the known membrane interactions of the complexin C-terminal domain and their potential relevance to its function, synaptic localization, and evolutionary history.

Indexed as

Adaptor Proteins, Vesicular TransportMembrane FusionNerve Tissue ProteinsSynaptic VesiclesExocytosisSNARE ProteinsAdaptor Proteins, Vesicular TransportNerve Tissue ProteinsSNARE Proteinsamphipathic helixcomplexincurvaturemembranesynapse

Identifiers

PMID35931110
PMCPMC9807284
OpenAlexW4289528565

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.