Evidence map›Paper›PMID 38168376›Full record

ArticlebioRxiv : the preprint server for biology2023

Single molecule studies of the native hair cell mechanosensory transduction complex.

Sarah Clark, Jaba Mitra, Johannes Elferich, April Goehring, Jingpeng Ge, Taekjip Ha, Eric Gouaux

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 6 institutions in 2 countries.

Sarah ClarkVollum Institute, Oregon Health & Science University, Portland, Oregon 97239, USA.ORCID 0000-0003-2805-2526
Jaba MitraDepartment of Materials Science and Engineering, University of Illinois Urbana-Champaign, IL 61801, USA.ORCID 0000-0001-6569-6203
Johannes ElferichVollum Institute, Oregon Health & Science University, Portland, Oregon 97239, USA.ORCID 0000-0002-9911-706X
April GoehringVollum Institute, Oregon Health & Science University, Portland, Oregon 97239, USA.ORCID 0000-0002-2592-6956
Jingpeng GeVollum Institute, Oregon Health & Science University, Portland, Oregon 97239, USA.ORCID 0000-0001-6164-1221
Taekjip HaDepartment of Biophysics and Biophysical Chemistry, Johns Hopkins University, Baltimore, MD 21215, USA.ORCID 0000-0003-2195-6258
Eric GouauxVollum Institute, Oregon Health & Science University, Portland, Oregon 97239, USA.ORCID 0000-0002-8549-2360
Oregon Health & Science University · USBoston Children's Hospital · USHoward Hughes Medical Institute · USOregon State University · USUMass Memorial Health Care · USUniversity of Illinois Urbana-Champaign · US

Funding

Supplement for childcare costs for NRSA fellowF32DC017894 · NIDCD · OREGON HEALTH & SCIENCE UNIVERSITY · PI CLARK, SARAH A · 2019 to 2021
$196k
NIDCD NIH HHS F32 DC017894
6 · The paper itself

Abstract

Hearing and balance rely on the conversion of a mechanical stimulus into an electrical signal, a process known as mechanosensory transduction (MT). In vertebrates, this process is accomplished by an MT complex that is located in hair cells of the inner ear. While the past three decades of research have identified many subunits that are important for MT and revealed interactions between these subunits, the composition and organization of a functional complex remains unknown. The major challenge associated with studying the MT complex is its extremely low abundance in hair cells; current estimates of MT complex quantity range from 3-60 attomoles per cochlea or utricle, well below the detection limit of most biochemical assays that are used to characterize macromolecular complexes. Here we describe the optimization of two single molecule assays, single molecule pull-down (SiMPull) and single molecule array (SiMoA), to study the composition and quantity of native mouse MT complexes. We demonstrate that these assays are capable of detecting and quantifying low attomoles of the native MT subunits protocadherin-15 (PCDH15) and lipoma HMGIC fusion partner-like protein 5 (LHFPL5). Our results illuminate the stoichiometry of PCDH15- and LHFPL5-containing complexes and establish SiMPull and SiMoA as productive methods for probing the abundance, composition, and arrangement of subunits in the native MT complex.

Identifiers

PMID38168376
PMCPMC10760052
OpenAlexW4389609943

What OpenQuestion holds

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LicenceCC BY
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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.