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  3. iMEM: Isolation of Plasma Membrane for Cryoelectron Microscopy.
 

iMEM: Isolation of Plasma Membrane for Cryoelectron Microscopy.

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BORIS DOI
10.7892/boris.91356
Date of Publication
December 6, 2016
Publication Type
Article
Division/Institute

Institut für Anatomie...

Author
Peitsch, Camille Françoise
Institut für Anatomie
Beckmann, Sven
Institut für Anatomie
Zuber, Benoîtorcid-logo
Institut für Anatomie
Subject(s)

600 - Technology::610...

Series
Structure
ISSN or ISBN (if monograph)
0969-2126
Publisher
Cell Press
Language
English
Publisher DOI
10.1016/j.str.2016.09.016
PubMed ID
27818102
Uncontrolled Keywords

actin cortex

blotting

cell-free system

cryoelectron tomograp...

electron microscopy

endocytosis

exocytosis

filter paper

large dense core vesi...

live fluorescence ima...

plasma membrane

Description
The plasma membrane and the cell cortex are essential parts of the eukaryotic cell. The plasma membrane delimitates the cell and mediates communication with the outside. The cell cortex is the submembrane cytoskeleton shaping the cell and is able to reorganize for the passage of material. To study events at and near the plasma membrane, cryoelectron microscopy (cryo-EM) may be used. Most intact cells are too thick for direct cryo-EM imaging. Generating cell-free membrane patches could be a means to study features at the plasma membrane. Here we present an unroofing method, termed iMEM (isolation of membrane patches for cryo-EM) where the plasma membrane is isolated directly on an EM grid. The in situ isolation of membrane patches has several advantages: it is a one-step procedure providing a higher throughput than focused-ion beam cryomilling. It enables the time-precise control over biochemical events before cryofixation.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/147090
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FileFile TypeFormatSizeLicensePublisher/Copright statementContent
1-s2.0-S0969212616303070-main.pdftextAdobe PDF4.42 MBpublished
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