Evidence map›Paper›PMID 37720554›Full record

ArticleFrontiers in molecular neuroscience2023

A toxin-based approach to neuropeptide and peptide hormone discovery.

Thomas Lund Koch, Joshua P Torres, Robert P Baskin, Paula Flórez Salcedo, Kevin Chase, Baldomero M Olivera, Helena Safavi-Hemami

Abstract read
In one paragraph

Article in Frontiers in molecular neuroscience, 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
–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

10 citing papers in PubMed.

  1. Article
  2. Toxins in disguise: Neuropeptide mimicry across animal venoms.General and comparative endocrinology · 2026
    Review
  3. Review
  4. Structural similarities reveal an expansive conotoxin family with a two-finger toxin fold.Protein science : a publication of the Protein Society · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Prey Shifts Drive Venom Evolution in Cone Snails.Molecular biology and evolution · 2024
    Article
  9. Review
  10. 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

7 authors.

Thomas Lund KochDepartment of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
Joshua P TorresDepartment of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
Robert P BaskinSchool of Biological Sciences, University of Utah, Salt Lake City, UT, United States.
Paula Flórez SalcedoDepartment of Neurobiology, University of Utah, Salt Lake City, UT, United States.
Kevin ChaseSchool of Biological Sciences, University of Utah, Salt Lake City, UT, United States.
Baldomero M OliveraSchool of Biological Sciences, University of Utah, Salt Lake City, UT, United States.
Helena Safavi-HemamiDepartment of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.

Funding

Q-ToF Mass Spectrometer for the University of Utah MS and Proteomics CoreS10OD018210 · OD · UNIVERSITY OF UTAH · PI COX, JAMES ERIC · 2015 to 2015
$530k
NIH HHS S10 OD018210
6 · The paper itself

Abstract

Peptide hormones and neuropeptides form a diverse class of bioactive secreted molecules that control essential processes in animals. Despite breakthroughs in peptide discovery, many signaling peptides remain undiscovered. Recently, we demonstrated the use of somatostatin-mimicking toxins from cone snails to identify the invertebrate ortholog of somatostatin. Here, we show that this toxin-based approach can be systematically applied to discover other unknown secretory peptides that are likely to have signaling function. Using large sequencing datasets, we searched for homologies between cone snail toxins and secreted proteins from the snails' prey. We identified and confirmed expression of five toxin families that share strong similarities with unknown secretory peptides from mollusks and annelids and in one case also from ecdysozoans. Based on several lines of evidence we propose that these peptides likely act as signaling peptides that serve important physiological functions. Indeed, we confirmed that one of the identified peptides belongs to the family of crustacean hyperglycemic hormone, a peptide not previously observed in Spiralia. We propose that this discovery pipeline can be broadly applied to other systems in which one organism has evolved molecules to manipulate the physiology of another.

Indexed as

Conuscrustacean hyperglycemic hormonehormoneneuropeptidetoxinsvenom

Identifiers

PMID37720554
PMCPMC10501145

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Registered trials

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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.