Evidence map›Paper›PMID 26953342›Full record

ArticleThe Journal of biological chemistry2016

Complex Formed between Intramembrane Metalloprotease SpoIVFB and Its Substrate, Pro-σK.

Yang Zhang, Sabyasachi Halder, Richard A Kerr, Daniel Parrell, Brandon Ruotolo, Lee Kroos

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.2field-weighted citation impact, top 41% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Interaction of intramembrane metalloprotease SpoIVFB with substrate Pro-σProceedings of the National Academy of Sciences of the United States of America · 2017
    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

6 authors at 2 institutions in 1 country.

Yang ZhangFrom the Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, Michigan 48824 and.
Sabyasachi HalderFrom the Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, Michigan 48824 and.
Richard A Kerrthe Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109.
Daniel ParrellFrom the Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, Michigan 48824 and.
Brandon Ruotolothe Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109.
Lee KroosFrom the Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, Michigan 48824 and kroos@msu.edu.
Michigan State University · USUniversity of Michigan–Ann Arbor · US

Funding

SWITCH GOVERNING BACILLUS MOTHER CELL GENE EXPRESSIONR01GM043585 · NIGMS · MICHIGAN STATE UNIVERSITY · PI KROOS, LEE R · 1995 to 2021
$4.8M
New Structural Mass Spectrometry Tools Applied to the Mitochondrial Membrane ProtR01GM105942 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ANDREWS, PHILIP C, RUOTOLO, BRANDON T · 2013 to 2016
$1.4M
NIGMS NIH HHS R01 GM043585NIGMS NIH HHS R01 GM105942
6 · The paper itself

Abstract

Intramembrane metalloproteases (IMMPs) are conserved from bacteria to humans and control many important signaling pathways, but little is known about how IMMPs interact with their substrates. SpoIVFB is an IMMP that cleaves Pro-σ(K) during Bacillus subtilis endospore formation. When catalytically inactive SpoIVFB was coexpressed with C-terminally truncated Pro-σ(K)(1-126) (which can be cleaved by active SpoIVFB) in Escherichia coli, the substrate dramatically improved solubilization of the enzyme from membranes with mild detergents. Both the Pro(1-20) and σ(K)(21-126) parts contributed to improving SpoIVFB solubilization from membranes, but only the σ(K) part was needed to form a stable complex with SpoIVFB in a pulldown assay. The last 10 residues of SpoIVFB were required for improved solubilization from membranes by Pro-σ(K)(1-126) and for normal interaction with the substrate. The inactive SpoIVFB·Pro-σ(K)(1-126)-His6 complex was stable during affinity purification and gel filtration chromatography. Disulfide cross-linking of the purified complex indicated that it resembled the complex formed in vivo Ion mobility-mass spectrometry analysis resulted in an observed mass consistent with a 4:2 SpoIVFB·Pro-σ(K)(1-126)-His6 complex. Stepwise photobleaching of SpoIVFB fused to a fluorescent protein supported the notion that the enzyme is tetrameric during B. subtilis sporulation. The results provide the first evidence that an IMMP acts as a tetramer, give new insights into how SpoIVFB interacts with its substrate, and lay the foundation for further biochemical analysis of the enzyme·substrate complex and future structural studies.

Indexed as

Bacillus subtilisBacterial ProteinsCell MembraneEndopeptidasesImmunoblottingMass SpectrometryMembrane ProteinsProtein PrecursorsSignal TransductionSubstrate SpecificityBacterial ProteinsEndopeptidasesMembrane ProteinsProtein PrecursorsspoIVFB protein, Bacillus subtilisBacillusbacterial signal transductionenzyme purificationenzyme-substrate interactionintramembrane proteolysismass spectrometry (MS)metalloenzymeprotein complexsigma factorsporulation

Identifiers

PMID26953342
PMCPMC4858981
OpenAlexW2294823859

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.