Evidence map›Paper›PMID 32483166›Full record

ArticleNature communications2020

A nanobody-based fluorescent reporter reveals human α-synuclein in the cell cytosol.

Christoph Gerdes, Natalia Waal, Thomas Offner, Eugenio F Fornasiero, Nora Wender, Hannes Verbarg, Ivan Manzini, Claudia Trenkwalder, Brit Mollenhauer, Timo Strohäker and 5 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 7% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
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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

15 authors at 4 institutions in 1 country.

Christoph GerdesDepartment of Neuro- and Sensory Physiology, University Medical Center Göttingen, D-37073, Göttingen, Germany.ORCID http://orcid.org/0000-0001-5351-5348
Natalia WaalCenter for Biostructural Imaging of Neurodegeneration (BIN), University Medical Center Göttingen, D-37073, Göttingen, Germany.ORCID http://orcid.org/0000-0002-2974-7699
Thomas OffnerInstitute of Animal Physiology, Department of Animal Physiology and Molecular Biomedicine, Justus-Liebig University Giessen, 35390, Giessen, Germany.
Eugenio F FornasieroDepartment of Neuro- and Sensory Physiology, University Medical Center Göttingen, D-37073, Göttingen, Germany.ORCID http://orcid.org/0000-0001-7643-4962
Nora WenderDepartment of Neuro- and Sensory Physiology, University Medical Center Göttingen, D-37073, Göttingen, Germany.
Hannes VerbargDepartment of Neuro- and Sensory Physiology, University Medical Center Göttingen, D-37073, Göttingen, Germany.
Ivan ManziniInstitute of Animal Physiology, Department of Animal Physiology and Molecular Biomedicine, Justus-Liebig University Giessen, 35390, Giessen, Germany.ORCID http://orcid.org/0000-0002-3575-9637
Claudia TrenkwalderDepartment of Neurosurgery, University Medical Center Göttingen, D-37075, Göttingen, Germany.
Brit MollenhauerParacelsus-Elena-Klinik, Klinikstraße 16, 34128, Kassel, Germany.
Timo StrohäkerGerman Center for Neurodegenerative Diseases (DZNE), Von-Siebold-Str. 3a, 37075, Göttingen, Germany.
Markus ZweckstetterGerman Center for Neurodegenerative Diseases (DZNE), Von-Siebold-Str. 3a, 37075, Göttingen, Germany.
Stefan BeckerDepartment for NMR-based Structural Biology, Max Planck Institute for Biophysical Chemistry, 37077, Göttingen, Germany.ORCID http://orcid.org/0000-0003-2041-5740
Silvio O RizzoliDepartment of Neuro- and Sensory Physiology, University Medical Center Göttingen, D-37073, Göttingen, Germany.
Fitnat Buket Basmanav *Department of Neuro- and Sensory Physiology, University Medical Center Göttingen, D-37073, Göttingen, Germany.
Felipe Opazo *Department of Neuro- and Sensory Physiology, University Medical Center Göttingen, D-37073, Göttingen, Germany. fopazo@gwdg.de.ORCID http://orcid.org/0000-0002-4968-9713
Universitätsmedizin Göttingen · DEGerman Center for Neurodegenerative Diseases · DEJustus-Liebig-Universität Gießen · DEMax Planck Institute for Biophysical Chemistry · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aggregation and spreading of α-Synuclein (αSyn) are hallmarks of several neurodegenerative diseases, thus monitoring human αSyn (hαSyn) in animal models or cell cultures is vital for the field. However, the detection of native hαSyn in such systems is challenging. We show that the nanobody NbSyn87, previously-described to bind hαSyn, also shows cross-reactivity for the proteasomal subunit Rpn10. As such, when the NbSyn87 is expressed in the absence of hαSyn, it is continuously degraded by the proteasome, while it is stabilized when it binds to hαSyn. Here, we exploit this feature to design a new Fluorescent Reporter for hαSyn (FluoReSyn) by fusing NbSyn87 to fluorescent proteins, which results in fluorescence signal fluctuations depending on the presence and amounts of intracellular hαSyn. We characterize this biosensor in cells and tissues to finally reveal the presence of transmittable αSyn in human cerebrospinal fluid, demonstrating the potential of FluoReSyn for clinical research and diagnostics.

Indexed as

AdultAgedAged, 80 and overalpha-SynucleinAnimalsCells, CulturedCytosolFemaleFluorescenceHEK293 CellsHumansLuminescent ProteinsMaleMicroscopy, Fluorescence, MultiphotonMiddle AgedNeuronsalpha-SynucleinLuminescent ProteinsRed Fluorescent ProteinSingle-Domain Antibodies

Identifiers

PMID32483166
PMCPMC7264335
OpenAlexW3031733595

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.