Evidence map›Paper›PMID 37333400›Full record

ArticlebioRxiv : the preprint server for biology2023

Quantifying turgor pressure in budding and fission yeasts based upon osmotic properties.

Joël Lemière, Fred Chang

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, 7 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Joël LemièreDepartment of Cell and Tissue Biology, University of San Francisco, CA, USA.
Fred ChangDepartment of Cell and Tissue Biology, University of San Francisco, CA, USA.
University of California, San Francisco · US

Funding

Mechanics of cell growth and divisionR35GM141796 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Fred Chang · 2021 to 2026
$3.7M
NIGMS NIH HHS R35 GM141796
6 · The paper itself

Abstract

Walled cells, such as plants, fungi, and bacteria cells, possess a high internal hydrostatic pressure, termed turgor pressure, that drives volume growth and contributes to cell shape determination. Rigorous measurement of turgor pressure, however, remains challenging, and reliable quantitative measurements, even in budding yeast are still lacking. Here, we present a simple and robust experimental approach to access turgor pressure in yeasts based upon the determination of isotonic concentration using protoplasts as osmometers. We propose three methods to identify the isotonic condition - 3D cell volume, cytoplasmic fluorophore intensity, and mobility of a cytGEMs nano-rheology probe - that all yield consistent values. Our results provide turgor pressure estimates of 1.0 ± 0.1 MPa for

Indexed as

cell volumecytoplasmic crowdingfluorescenceprotoplastSaccharomyces cerevisiaeSchizosaccharomyces. japonicasSchizosaccharomyces pombeturgor pressureyeast

Identifiers

PMID37333400
PMCPMC10274794
OpenAlexW4379875727

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.