Evidence map›Paper›PMID 42681351›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Preparation of Plasma Membrane Vesicles, Lysosomes, Proteoliposomes and Alternative Sample Types for SSM-Based Electrophysiology.

Andre Bazzone, Rocco Zerlotti, Maximilian Kellner, Nidish Ponath Sadanandan

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Article in Methods in molecular biology (Clifton, N.J.), 2026. 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
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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.

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

4 authors.

Andre BazzoneNanion Technologies GmbH, Ganghoferstraße, D-80339, Munich, Germany. andre.bazzone@nanion.de.
Rocco ZerlottiNanion Technologies GmbH, Ganghoferstraße, D-80339, Munich, Germany.
Maximilian KellnerNanion Technologies GmbH, Ganghoferstraße, D-80339, Munich, Germany.
Nidish Ponath SadanandanPharmacology Department, Fraunhofer Gesellschaft FhG, ITMP-IIP, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Solid-supported membrane-based electrophysiology (SSME) is a vital technique for characterizing electrogenic membrane protein activity, with reliable measurements critically dependent on high-quality sample preparation. This chapter presents a comprehensive, step-by-step protocol for the purification of plasma membrane vesicles and lysosomes from mammalian cell culture, specifically optimized for SSME recordings. The method combines nitrogen decompression with discontinuous sucrose gradient centrifugation to maximize purity and yield, thereby substantially improving the signal-to-noise ratio compared to crude membrane extracts. To evaluate the purity of the resulting membrane fractions, we analyzed the enrichment of 14 marker proteins representing not only plasma membrane and lysosomes, but also endosomes, endoplasmic reticulum, Golgi apparatus, mitochondria, and other organelles. In addition, the chapter provides guidance on adapting the protocol to different experimental requirements, including alternative cell disruption techniques, approaches for enriching other organelles, and the use of crude membrane preparations in high-throughput screening applications. Alternative sample sources and preparation strategies are also discussed, encompassing bacterial membranes, native tissues, cell-free expression systems, and intact cultured cells, with references to established protocols. A dedicated section describes the generation of proteoliposomes-an important complementary sample type that offers greater flexibility for studying low-turnover transporters and for achieving precise control of membrane composition. Collectively, this methodological framework serves as a basis for SSME sample preparation and underscores the versatility of SSME.

Indexed as

Cell FractionationCell MembraneElectrophysiologyLysosomesProteolipidsAnimalsCell-Free SystemCentrifugation, Density GradientElectrophysiological PhenomenaHumansProteolipidsproteoliposomesEnrichmentIsolationMembranesMembrane transportOrganellesPurificationSSM-based electrophysiologySSMESURFE2R

Identifiers

PMID42681351

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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.