Evidence map›Paper›PMID 25034694›Full record

ArticleNucleic acids research2014

In vivo co-localization of enzymes on RNA scaffolds increases metabolic production in a geometrically dependent manner.

Gairik Sachdeva, Abhishek Garg, David Godding, Jeffrey C Way, Pamela A Silver

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 1 pooled it
8.0field-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

58 citing papers in PubMed, 1 synthesis or guideline pooled it, 159 citations in OpenAlex.

  1. Pooled it
  2. Review
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  7. Review
  8. Unleashing the potential of catalytic RNAs to combat mis-spliced transcripts.Frontiers in bioengineering and biotechnology · 2023
    Review
  9. Application of artificial scaffold systems in microbial metabolic engineering.Frontiers in bioengineering and biotechnology · 2023
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Enzyme assemblies on demand.Nature chemical biology · 2022
    Article
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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

5 authors at 3 institutions in 2 countries.

Gairik SachdevaSchool of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138, USA Department of Systems Biology, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115, USA Wyss Institute for Biologically Inspired Engineering, 3 Blackfan St., Boston, MA 02115, USA.
Abhishek GargDepartment of Systems Biology, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115, USA.
David GoddingDepartment of Life Sciences, Imperial College London, London SW7 2AZ, UK.
Jeffrey C WayWyss Institute for Biologically Inspired Engineering, 3 Blackfan St., Boston, MA 02115, USA.
Pamela A SilverDepartment of Systems Biology, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115, USA Wyss Institute for Biologically Inspired Engineering, 3 Blackfan St., Boston, MA 02115, USA pamela_silver@hms.harvard.edu.
Harvard University · USCenter for Systems Biology · USImperial College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Co-localization of biochemical processes plays a key role in the directional control of metabolic fluxes toward specific products in cells. Here, we employ in vivo scaffolds made of RNA that can bind engineered proteins fused to specific RNA binding domains. This allows proteins to be co-localized on RNA scaffolds inside living Escherichia coli. We assembled a library of eight aptamers and corresponding RNA binding domains fused to partial fragments of fluorescent proteins. New scaffold designs could co-localize split green fluorescent protein fragments to produce activity as measured by cell-based fluorescence. The scaffolds consisted of either single bivalent RNAs or RNAs designed to polymerize in one or two dimensions. The new scaffolds were used to increase metabolic output from a two-enzyme pentadecane production pathway that contains a fatty aldehyde intermediate, as well as three and four enzymes in the succinate production pathway. Pentadecane synthesis depended on the geometry of enzymes on the scaffold, as determined through systematic reorientation of the acyl-ACP reductase fusion by rotation via addition of base pairs to its cognate RNA aptamer. Together, these data suggest that intra-cellular scaffolding of enzymatic reactions may enhance the direct channeling of a variety of substrates.

Indexed as

Metabolic Networks and PathwaysAlkanesAptamers, NucleotideEnzymesEscherichia coliFluorescent DyesGreen Fluorescent ProteinsMetabolic EngineeringProtein Structure, TertiaryRecombinant Fusion ProteinsRNARNA-Binding ProteinsSuccinic AcidAlkanesAptamers, NucleotideEnzymesFluorescent DyesGreen Fluorescent ProteinspentadecaneRecombinant Fusion ProteinsRNARNA-Binding ProteinsSuccinic Acid

Identifiers

PMID25034694
PMCPMC4132732
OpenAlexW2104961996

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.