Evidence map›Paper›PMID 30010220›Full record

ArticleMolecular microbiology2018

Species- and C-terminal linker-dependent variations in the dynamic behavior of FtsZ on membranes in vitro.

Kousik Sundararajan, Anthony Vecchiarelli, Kiyoshi Mizuuchi, Erin D Goley

Abstract read
In one paragraph

Article in Molecular microbiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. GTPase activity regulates FtsZ ring positioning inMolecular biology of the cell · 2024
    Article
  4. Review
  5. Dynamic Assembly/Disassembly ofInternational journal of molecular sciences · 2021
    Article
  6. FtsZ dynamics in bacterial division: What, how, and why?Current opinion in cell biology · 2021
    Review
  7. Review
  8. Article
  9. Bacterial cell division at a glance.Journal of cell science · 2020
    Review
  10. Article
  11. 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

4 authors.

Kousik SundararajanDepartment of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.ORCID 0000-0002-1375-5491
Anthony VecchiarelliMolecular, Cellular, and Developmental Biology, University of Michigan College of Literature Science and the Arts, Ann Arbor, MI, 48109, USA.ORCID 0000-0002-6198-3245
Kiyoshi MizuuchiLaboratory of Molecular Biology, National Institute of Diabetes, and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, 20814, USA.
Erin D GoleyDepartment of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.ORCID 0000-0002-8518-2303

Funding

Study of the mechanism of septum localization during bacterial cell divisionZIADK036164 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI MIZUUCHI, KIYOSHI · 2009 to 2025
$12.7M
Regulation and Mechanism of the C. Crescentus Cytokinetic RingR01GM108640 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI GOLEY, ERIN D · 2015 to 2019
$1.6M
Intramural NIH HHS ZIA DK036164NIGMS NIH HHS R01 GM108640
6 · The paper itself

Abstract

Bacterial cell division requires the assembly of FtsZ protofilaments into a dynamic structure called the 'Z-ring'. The Z-ring recruits the division machinery and directs local cell wall remodeling for constriction. The organization and dynamics of protofilaments within the Z-ring coordinate local cell wall synthesis during cell constriction, but their regulation is largely unknown. The disordered C-terminal linker (CTL) region of Caulobacter crescentus FtsZ (CcFtsZ) regulates polymer structure and turnover in solution in vitro, and regulates Z-ring structure and activity of cell wall enzymes in vivo. To investigate the contributions of the CTL to the polymerization properties of FtsZ on its physiological platform, the cell membrane, we reconstituted CcFtsZ polymerization on supported lipid bilayers (SLB) and visualized polymer dynamics and structure using total internal reflection fluorescence microscopy. Unlike Escherichia coli FtsZ protofilaments that organized into large, bundled patterns, CcFtsZ protofilaments assembled into small, dynamic clusters on SLBs. Moreover, CcFtsZ lacking its CTL formed large networks of straight filament bundles that underwent slower turnover than the dynamic clusters of wildtype FtsZ. Our in vitro characterization provides novel insights into species- and CTL-dependent differences between FtsZ assembly properties that are relevant to Z-ring assembly and function on membranes in vivo.

Indexed as

Bacterial ProteinsCaulobacter crescentusCell DivisionCell MembraneCell WallCytoskeletal ProteinsCytoskeletonEscherichia coliLipid BilayersMaleimidesMicroscopy, FluorescencePhosphatidylcholinesPhosphatidylglycerolsProtein Multimerization1,2-dioleoyl-sn-glycero-3-phosphoglycerol1,2-oleoylphosphatidylcholineAlexa Fluor 488 C5-maleimideBacterial ProteinsCytoskeletal ProteinsFtsZ protein, BacteriaLipid BilayersMaleimidesPhosphatidylcholinesPhosphatidylglycerols

Identifiers

PMID30010220
PMCPMC6195856

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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.