Evidence map›Paper›PMID 37860658›Full record

ReviewChemical science2023

From random to rational: improving enzyme design through electric fields, second coordination sphere interactions, and conformational dynamics.

Shobhit S Chaturvedi, Daniel Bím, Christo Z Christov, Anastassia N Alexandrova

Open access · diamondAbstract readReview
In one paragraph

Review in Chemical science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Functional dynamics of water in New Delhi metallo-β-lactamase catalysis.Protein science : a publication of the Protein Society · 2026
    Article
  6. Article
  7. s_mmpbsa: A Lite and Cross-Platform MM-PBSA Program.Molecules (Basel, Switzerland) · 2026
    Article
  8. Review
  9. Oriented Electric Fields─Universal Catalysts.Accounts of chemical research · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Design of a light and CaProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  17. Article
  18. Review
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

4 authors at 2 institutions in 1 country.

Shobhit S ChaturvediDepartment of Chemistry and Biochemistry, University of California, Los Angeles California 90095 USA ana@chem.ucla.edu.ORCID https://orcid.org/0000-0003-4977-5600
Daniel BímDepartment of Chemistry and Biochemistry, University of California, Los Angeles California 90095 USA ana@chem.ucla.edu.ORCID https://orcid.org/0000-0003-3100-4293
Christo Z ChristovDepartment of Chemistry, Michigan Technological University Houghton Michigan 49931 USA.ORCID https://orcid.org/0000-0002-4481-0246
Anastassia N AlexandrovaDepartment of Chemistry and Biochemistry, University of California, Los Angeles California 90095 USA ana@chem.ucla.edu.ORCID https://orcid.org/0000-0002-3003-1911
Michigan Technological University · USUniversity of California, Los Angeles · US

Funding

Redox enzymes - tuning and designR01GM134047 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ALEXANDROVA, ANASTASSIA N, YANG, JENNY · 2019 to 2022
$1.3M
Understanding the Ligand Binding by Non-Heme Fe(II)- and 2-Oxoglutarate-Dependent Histone DemethylasesR15GM139118 · NIGMS · MICHIGAN TECHNOLOGICAL UNIVERSITY · PI CHRISTOV, CHRISTO ZHIVKOV · 2021 to 2024
$786k
NIGMS NIH HHS R01 GM134047NIGMS NIH HHS R15 GM139118
6 · The paper itself

Abstract

Enzymes are versatile and efficient biological catalysts that drive numerous cellular processes, motivating the development of enzyme design approaches to tailor catalysts for diverse applications. In this perspective, we investigate the unique properties of natural, evolved, and designed enzymes, recognizing their strengths and shortcomings. We highlight the challenges and limitations of current enzyme design protocols, with a particular focus on their limited consideration of long-range electrostatic and dynamic effects. We then delve deeper into the impact of the protein environment on enzyme catalysis and explore the roles of preorganized electric fields, second coordination sphere interactions, and protein dynamics for enzyme function. Furthermore, we present several case studies illustrating successful enzyme-design efforts incorporating enzyme strategies mentioned above to achieve improved catalytic properties. Finally, we envision the future of enzyme design research, spotlighting the challenges yet to be overcome and the synergy of intrinsic electric fields, second coordination sphere interactions, and conformational dynamics to push the state-of-the-art boundaries.

Identifiers

PMID37860658
PMCPMC10583697
OpenAlexW4386710792

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.