Evidence map›Paper›PMID 25678711›Full record

ArticleThe Journal of biological chemistry2015

HypE-specific nanobodies as tools to modulate HypE-mediated target AMPylation.

Matthias C Truttmann, Qin Wu, Sarah Stiegeler, Joao N Duarte, Jessica Ingram, Hidde L Ploegh

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

28 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
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  7. Site-Specifically Conjugated Single-Domain Antibody Successfully Identifies Glypican-3-Expressing Liver Cancer by Immuno-PET.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2023
    Article
  8. Article
  9. The Alarmone Diadenosine Tetraphosphate as a Cosubstrate for Protein AMPylation.Angewandte Chemie (International ed. in English) · 2023
    Article
  10. Article
  11. Production of an Active, Human Membrane Protein inInternational journal of molecular sciences · 2022
    Article
  12. The AMPylase FIC-1 modulates TGF-β signaling inFrontiers in molecular neuroscience · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Exploring cellular biochemistry with nanobodies.The Journal of biological chemistry · 2020
    Review
  17. Article
  18. Article
  19. Article
  20. 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.

Matthias C TruttmannFrom the Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142 and.
Qin WuFrom the Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142 and.
Sarah StiegelerFrom the Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142 and.
Joao N DuarteFrom the Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142 and.
Jessica IngramFrom the Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142 and.
Hidde L PloeghFrom the Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142 and the Massachusetts Institute of Technology, Cambridge, Massachusetts 02139 ploegh@wi.mit.edu.
Whitehead Institute for Biomedical Research · USMassachusetts Institute of Technology · US

Funding

A new strategy to disrupt protein-protein interactions in eukaryotic cells.DP1GM106409 · NIGMS · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI PLOEGH, HIDDE L. · 2012 to 2016
$4.8M
NIGMS NIH HHS DP1 GM106409
6 · The paper itself

Abstract

The covalent addition of mono-AMP to target proteins (AMPylation) by Fic domain-containing proteins is a poorly understood, yet highly conserved post-translational modification. Here, we describe the generation, evaluation, and application of four HypE-specific nanobodies: three that inhibit HypE-mediated target AMPylation in vitro and one that acts as an activator. All heavy chain-only antibody variable domains bind HypE when expressed as GFP fusions in intact cells. We observed localization of HypE at the nuclear envelope and further identified histones H2-H4, but not H1, as novel in vitro targets of the human Fic protein. Its role in histone modification provides a possible link between AMPylation and regulation of gene expression.

Indexed as

Adenosine MonophosphateAmino Acid SequenceCarrier ProteinsCell LineFlow CytometryHumansMembrane ProteinsMolecular Sequence DataNucleotidyltransferasesSequence Homology, Amino AcidSingle-Domain AntibodiesAdenosine MonophosphateCarrier ProteinsFICD protein, humanMembrane ProteinsNucleotidyltransferasesSingle-Domain AntibodiesAMPylationFic ProteinsHistone ModificationHypENuclear MembranePhage DisplayPost-translational Modification (PTM)Recombinant Protein ExpressionVHHs

Identifiers

PMID25678711
PMCPMC4424278
OpenAlexW2036946921

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.