Evidence map›Paper›PMID 29632258›Full record

ArticlePhilosophical transactions of the Royal Society of London. Series B, Biological sciences2018

Reverse and forward engineering of protein pattern formation.

Simon Kretschmer, Leon Harrington, Petra Schwille

Abstract read
In one paragraph

Article in Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Self-organization: the fundament of cell biology.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2018
    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

3 authors.

Simon KretschmerDepartment of Cellular and Molecular Biophysics, Max-Planck-Institute of Biochemistry, 82152 Martinsried, Germany.
Leon HarringtonDepartment of Cellular and Molecular Biophysics, Max-Planck-Institute of Biochemistry, 82152 Martinsried, Germany.
Petra SchwilleDepartment of Cellular and Molecular Biophysics, Max-Planck-Institute of Biochemistry, 82152 Martinsried, Germany schwille@biochem.mpg.de.ORCID 0000-0002-6106-4847

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Living systems employ protein pattern formation to regulate important life processes in space and time. Although pattern-forming protein networks have been identified in various prokaryotes and eukaryotes, their systematic experimental characterization is challenging owing to the complex environment of living cells. In turn, cell-free systems are ideally suited for this goal, as they offer defined molecular environments that can be precisely controlled and manipulated. Towards revealing the molecular basis of protein pattern formation, we outline two complementary approaches: the biochemical reverse engineering of reconstituted networks and the de novo design, or forward engineering, of artificial self-organizing systems. We first illustrate the reverse engineering approach by the example of the

Indexed as

Molecular ConformationProtein BiosynthesisCell Cycle ProteinsEscherichia coliEscherichia coli ProteinsPhase TransitionCell Cycle ProteinsEscherichia coli ProteinsMinE protein, E coliin vitro reconstitutionMin systempattern formationreaction–diffusion systemsself-organizationsynthetic biology

Identifiers

PMID29632258
PMCPMC5904292

What OpenQuestion holds

Textmetadata
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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.