Protocol for endolysosomal proteomics in goat atrial tissue using a refined density-gradient approach

Here, we present a protocol to analyze endolysosomal (EL) proteins in goat atrial fibrillation (AF) tissue using a modified density-gradient, proteomic-based fractionation. This method separates organelles from tissue lysate, isolating sarcoplasmic reticulum, mitochondria (1.3 g/mL), and EL (1.04 g/mL) with minimal contamination. The protocol includes tissue isolation, homogenization, density-gradient processing, peptide analysis, data analysis, and protein network identification using discontinuous Percoll and sucrose gradients; it supports molecular and proteomic studies. For complete details on the use and execution of this protocol, please refer to Ayagama et al.<sup>1</sup> and Ayagama et al.<sup>2</sup>.

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Publication Details

Journal
STAR Protocols
Published
2025-12-01
DOI
https://doi.org/10.1016/j.xpro.2025.104248
Citations
1
Primary Topic
Cellular transport and secretion
Type
article
Field-Weighted Citation Impact
1.15
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article

Protocol for endolysosomal proteomics in goat atrial tissue using a refined density-gradient approach

G. Berridge, Román Fischer, Ulrich Schotten, Rebecca A. Capel et al.
1 citations
STAR Protocols
Cellular transport and secretion
1.15
article

Protocol for endolysosomal proteomics in goat atrial tissue using a refined density-gradient approach

G. Berridge, Román Fischer, Ulrich Schotten, Rebecca A. Capel, Sander Verheule, Thamali Ayagama, Rebecca A.B. Burton
article en
1 citations

Abstract

Here, we present a protocol to analyze endolysosomal (EL) proteins in goat atrial fibrillation (AF) tissue using a modified density-gradient, proteomic-based fractionation. This method separates organelles from tissue lysate, isolating sarcoplasmic reticulum, mitochondria (1.3 g/mL), and EL (1.04 g/mL) with minimal contamination. The protocol includes tissue isolation, homogenization, density-gradient processing, peptide analysis, data analysis, and protein network identification using discontinuous Percoll and sucrose gradients; it supports molecular and proteomic studies. For complete details on the use and execution of this protocol, please refer to Ayagama et al.<sup>1</sup> and Ayagama et al.<sup>2</sup>.

STAR ProtocolsVol. 6(4)
University of Liverpool (GB), Maastricht University (NL), University of Oxford (GB), Liverpool Heart and Chest Hospital (GB)
Openalex Percentile: Top 17%
Cellular transport and secretion
1.15
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