Evidence map›Paper›PMID 31100274›Full record

ReviewChemico-biological interactions2019

The evolution of phosphotriesterase for decontamination and detoxification of organophosphorus chemical warfare agents.

Andrew N Bigley, Frank M Raushel

Open access · greenAbstract readReview
In one paragraph

Review in Chemico-biological interactions, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
12.5field-weighted citation impact, top 2% 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

25 citing papers in PubMed, 102 citations in OpenAlex.

  1. The Discovery ofACS catalysis · 2026
    Article
  2. Catalytic pBiochemistry · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Supercharged Phosphotriesterase for improved Paraoxon activity.Protein engineering, design & selection : PEDS · 2024
    Article
  12. Review
  13. Article
  14. Article
  15. Bacterial Membrane Vesicles for In Vitro Catalysis.Bioengineering (Basel, Switzerland) · 2023
    Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. 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 1 institution in 1 country.

Andrew N BigleyDepartment of Chemistry, Texas A&M University, College Station, TX, 77843, USA.
Frank M RaushelDepartment of Chemistry, Texas A&M University, College Station, TX, 77843, USA. Electronic address: raushel@tamu.edu.
Texas A&M University · US

Funding

Enzymatic Hydrolysis of Organophosphate EstersR01GM116894 · NIGMS · TEXAS A&M UNIVERSITY · PI RAUSHEL, FRANK M. · 2017 to 2020
$1.1M
NIGMS NIH HHS R01 GM116894
6 · The paper itself

Abstract

The organophosphorus chemical warfare agents were initially synthesized in the 1930's and are some of the most toxic compounds ever discovered. The standard means of decontamination are either harsh chemical hydrolysis or high temperature incineration. Given the continued use of chemical warfare agents there are ongoing efforts to develop gentle environmentally friendly means of decontamination and medical counter measures to chemical warfare agent intoxication. Enzymatic decontamination offers the benefits of extreme specificity and mild conditions, allowing their use for both environmental and medical applications. The most promising enzyme for decontamination of the organophosphorus chemical warfare agents is the enzyme phosphotriesterase from Pseudomonas diminuta. However, the catalytic activity of the wild-type enzyme with the chemical warfare agents falls far below that seen with its best substrates, and its stereochemical preference is for the less toxic enantiomer of the chiral phosphorus center found in most chemical warfare agents. Rational design efforts have succeeded in the dramatic improvement of the stereochemical preference of PTE for the more toxic enantiomers. Directed evolution experiments, including site-saturation mutagenesis, targeted error-prone PCR, computational design, and quantitative library analysis, have systematically improved the catalytic activity against the chemical warfare nerve agents. These efforts have resulted in greater than 4-orders of magnitude improvement in catalytic activity and have led to the identification of variants that are highly effective at detoxifying both G-type and V-type nerve agents. The best of these variants have the ability to prevent intoxication when delivered as a post-exposure treatment for VX and as a pre-exposure treatment for G-agent intoxication with observed protective factors up to 60-fold. Combining the best variant, H257Y/L303T, with a PCB polymer coating has enabled the development of a long lasting circulating prophylactic treatment that is highly effective against sarin.

Indexed as

Evolution, MolecularBacterial ProteinsChemical Warfare AgentsDecontaminationInactivation, MetabolicOrganothiophosphorus CompoundsPhosphoric Triester HydrolasesPseudomonasStereoisomerismBacterial ProteinsChemical Warfare AgentsOrganothiophosphorus CompoundsPhosphoric Triester HydrolasesVX-agentChemical warfare agentsEnzyme evolutionNerve agentOrganophosphateOrganophosphate hydrolasePhosphotriesterase

Identifiers

PMID31100274
PMCPMC6622166
OpenAlexW2945956305

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.