Evidence map›Paper›PMID 33352834›Full record

ArticleToxins2020

Engineering an Effective Human SNAP-23 Cleaving Botulinum Neurotoxin A Variant.

Stefan Sikorra, Sarah Donald, Mark Elliott, Susan Schwede, Shu-Fen Coker, Adam P Kupinski, Vineeta Tripathi, Keith Foster, Matthew Beard, Thomas Binz

Open access · goldAbstract read
In one paragraph

Article in Toxins, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Probing the properties of PTEN specific botulinum toxin type E mutants.Journal of neural transmission (Vienna, Austria : 1996) · 2025
    Article
  4. Targeted degradation of α-Synuclein using an evolved botulinum toxin protease.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Review
  6. Review
  7. 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

10 authors at 2 institutions in 2 countries.

Stefan SikorraInstitut für Zellbiochemie, OE 4310, Medizinische Hochschule Hannover, 30623 Hannover, Germany.
Sarah DonaldIpsen Bioinnovation, 102 Park Drive, Milton Park, Abingdon OX14 4RY, UK.
Mark ElliottIpsen Bioinnovation, 102 Park Drive, Milton Park, Abingdon OX14 4RY, UK.
Susan SchwedeInstitut für Zellbiochemie, OE 4310, Medizinische Hochschule Hannover, 30623 Hannover, Germany.
Shu-Fen CokerIpsen Bioinnovation, 102 Park Drive, Milton Park, Abingdon OX14 4RY, UK.
Adam P KupinskiIpsen Bioinnovation, 102 Park Drive, Milton Park, Abingdon OX14 4RY, UK.
Vineeta TripathiIpsen Bioinnovation, 102 Park Drive, Milton Park, Abingdon OX14 4RY, UK.
Keith FosterIpsen Bioinnovation, 102 Park Drive, Milton Park, Abingdon OX14 4RY, UK.
Matthew BeardIpsen Bioinnovation, 102 Park Drive, Milton Park, Abingdon OX14 4RY, UK.
Thomas BinzInstitut für Zellbiochemie, OE 4310, Medizinische Hochschule Hannover, 30623 Hannover, Germany.ORCID 0000-0001-9133-3617
Ipsen (United Kingdom) · GBMedizinische Hochschule Hannover · DE

Funding

Ipsen none
6 · The paper itself

Abstract

Botulinum neurotoxin (BoNT) serotype A inhibits neurotransmitter release by cleaving SNAP-25 and represents an established pharmaceutical for treating medical conditions caused by hyperactivity of cholinergic nerves. Oversecretion from non-neuronal cells is often also the cause of diseases. Notably, excessive release of inflammatory messengers is thought to contribute to diseases such as chronic obstructive pulmonary disease, asthma, diabetes etc. The expansion of its application to these medical conditions is prevented because the major non-neuronal SNAP-25 isoform responsible for exocytosis, SNAP-23, is, in humans, virtually resistant to BoNT/A. Based on previous structural data and mutagenesis studies of SNAP-23 we optimized substrate binding pockets of the enzymatic domain for interaction with SNAP-23. Systematic mutagenesis and rational design yielded the mutations E148Y, K166F, S254A, and G305D, each of which individually increased the activity of LC/A against SNAP-23 between 3- to 23-fold. The assembled quadruple mutant showed approximately 2000-fold increased catalytic activity against human SNAP-23 in in vitro cleavage assays. A comparable increase in activity was recorded for the full-length BoNT/A quadruple mutant tested in cultivated primary neurons transduced with a fluorescently tagged-SNAP-23 encoding gene. Equipped with a suitable targeting domain this quadruple mutant promises to complete successfully tests in cells of the immune system.

Indexed as

Amino Acid SequenceAnimalsBotulinum Toxins, Type ACells, CulturedDose-Response Relationship, DrugHEK293 CellsHumansNeuronsProtein EngineeringProtein Structure, SecondaryQb-SNARE ProteinsQc-SNARE ProteinsRatsRats, Sprague-DawleyBotulinum Toxins, Type AQb-SNARE ProteinsQc-SNARE ProteinsSNAP23 protein, humanbotulinum toxinscreening methodSNAP-23SNAP-25substrate specificityzinc protease

Identifiers

PMID33352834
PMCPMC7766560
OpenAlexW3115213141

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.