Evidence map›Paper›PMID 35448360›Full record

ArticleMembranes2022

Dynamic Distribution of ASIC1a Channels and Other Proteins within Cells Detected through Fractionation.

Libia Catalina Salinas Castellanos, Rodolfo Gabriel Gatto, Silvia Adriana Menchón, Matías Blaustein, Osvaldo Daniel Uchitel, Carina Weissmann

Abstract read
In one paragraph

Article in Membranes, 2022. 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

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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.

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

6 authors.

Libia Catalina Salinas CastellanosInstituto de Fisiología Biologia Molecular y Neurociencias (IFIBYNE), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Departamento de Fisiología, Biología Molecular y Celular (DFBMC), University of Buenos Aires (UBA), Buenos Aires 1428, Argentina.
Rodolfo Gabriel GattoDepartment of Bioengineering, University of Illinois at Chicago, Chicago, IL 60607, USA.ORCID 0000-0003-2170-6662
Silvia Adriana MenchónIFEG-CONICET and FaMAF-Universidad Nacional de Córdoba, Ciudad Universitaria, Córdoba 5016, Argentina.ORCID 0000-0002-2142-2515
Matías BlausteinDepartamento de Fisiología, Biología Molecular y Celular (DFBMC), Facultad de Ciencias Exactas y Naturales (FCEyN), Instituto de Biociencias, Biotecnología y Biología Traslacional (iB3), University of Buenos Aires (UBA), Buenos Aires 1428, Argentina.ORCID 0000-0001-6309-6888
Osvaldo Daniel UchitelInstituto de Fisiología Biologia Molecular y Neurociencias (IFIBYNE), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Departamento de Fisiología, Biología Molecular y Celular (DFBMC), University of Buenos Aires (UBA), Buenos Aires 1428, Argentina.ORCID 0000-0002-8909-6787
Carina WeissmannInstituto de Fisiología Biologia Molecular y Neurociencias (IFIBYNE), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Departamento de Fisiología, Biología Molecular y Celular (DFBMC), University of Buenos Aires (UBA), Buenos Aires 1428, Argentina.ORCID 0000-0002-7196-5390

Funding

Agencia Nacional de Promoción Científica y Tecnológica (ANPCYT) PICT 2016-3642Takeda Pharmaceuticals International AG Singapore Branch IIR-AR-002659Universidad de Buenos Aires Ciencia y Tecnología [UBA-CYT] Grant 01/Q666 (20020130100666BA;
6 · The paper itself

Abstract

Proteins in eukaryotic cells reside in different cell compartments. Many studies require the specific localization of proteins and the detection of any dynamic changes in intracellular protein distribution. There are several methods available for this purpose that rely on the fractionation of the different cell compartments. Fractionation protocols have evolved since the first use of a centrifuge to isolate organelles. In this study, we described a simple method that involves the use of a tabletop centrifuge and different detergents to obtain cell fractions enriched in cytosolic (Cyt), plasma membrane (PM), membranous organelle (MO), and nuclear (Nu) proteins and identify the proteins in each fraction. This method serves to identify transmembrane proteins such as channel subunits as well as PM-embedded or weakly associated proteins. This protocol uses a minute amount of cell material and typical equipment present in laboratories, and it takes approximately 3 h. The process was validated using endogenous and exogenous proteins expressed in the HEK293T cell line that were targeted to each compartment. Using a specific stimulus as a trigger, we showed and quantified the shuttling of a protein channel (ASIC1a, acid sensing ion channel) from the MO fraction to the PM fraction and the shuttling of a kinase from a cytosolic location to a nuclear location.

Indexed as

distributionfractionationplasma-membrane-associated proteinstraffickingtranslocation

Identifiers

PMID35448360
PMCPMC9027401

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