Evidence map›Paper›PMID 31509711›Full record

ArticleJournal of the American Chemical Society2019

Breaking Symmetry: Engineering Single-Chain Dimeric Streptavidin as Host for Artificial Metalloenzymes.

Shuke Wu, Yi Zhou, Johannes G Rebelein, Miriam Kuhn, Hendrik Mallin, Jingming Zhao, Nico V Igareta, Thomas R Ward

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2019. 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
–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

18 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Rational design of allosteric switchable catalysts.Exploration (Beijing, China) · 2022
    Review
  9. Article
  10. Article
  11. Article
  12. Recent trends in biocatalysis.Chemical Society reviews · 2021
    Review
  13. Artificial Metalloproteins with Dinuclear Iron-Hydroxido Centers.Journal of the American Chemical Society · 2021
    Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. 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

8 authors.

Shuke WuDepartment of Chemistry , University of Basel , BPR 1096, Mattenstrasse 24a , CH-4058 Basel , Switzerland.ORCID 0000-0003-0914-9277
Yi ZhouDepartment of Chemistry , University of Basel , BPR 1096, Mattenstrasse 24a , CH-4058 Basel , Switzerland.ORCID 0000-0003-3467-193X
Johannes G RebeleinDepartment of Chemistry , University of Basel , BPR 1096, Mattenstrasse 24a , CH-4058 Basel , Switzerland.ORCID 0000-0003-2560-716X
Miriam KuhnDepartment of Chemistry , University of Basel , BPR 1096, Mattenstrasse 24a , CH-4058 Basel , Switzerland.
Hendrik MallinDepartment of Chemistry , University of Basel , BPR 1096, Mattenstrasse 24a , CH-4058 Basel , Switzerland.
Jingming ZhaoDepartment of Chemistry , University of Basel , BPR 1096, Mattenstrasse 24a , CH-4058 Basel , Switzerland.ORCID 0000-0001-7104-8990
Nico V IgaretaDepartment of Chemistry , University of Basel , BPR 1096, Mattenstrasse 24a , CH-4058 Basel , Switzerland.
Thomas R WardDepartment of Chemistry , University of Basel , BPR 1096, Mattenstrasse 24a , CH-4058 Basel , Switzerland.ORCID 0000-0001-8602-5468

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The biotin-streptavidin technology has been extensively exploited to engineer artificial metalloenzymes (ArMs) that catalyze a dozen different reactions. Despite its versatility, the homotetrameric nature of streptavidin (Sav) and the noncooperative binding of biotinylated cofactors impose two limitations on the genetic optimization of ArMs: (i) point mutations are reflected in all four subunits of Sav, and (ii) the noncooperative binding of biotinylated cofactors to Sav may lead to an erosion in the catalytic performance, depending on the cofactor:biotin-binding site ratio. To address these challenges, we report on our efforts to engineer a (monovalent) single-chain dimeric streptavidin (scdSav) as scaffold for Sav-based ArMs. The versatility of scdSav as host protein is highlighted for the asymmetric transfer hydrogenation of prochiral imines using [Cp*Ir(biot-

Indexed as

Binding SitesBiotinBiotinylationCatalysisChemical EngineeringChromatography, AffinityEscherichia coliHydrogenationIridiumKineticsMetalloproteinsOrganometallic CompoundsStereoisomerismStreptavidinBiotinIridiumMetalloproteinsOrganometallic CompoundsStreptavidin

Identifiers

PMID31509711
PMCPMC6805045

What OpenQuestion holds

Textmetadata
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.