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Separation of Thylakoid Protein Complexes with Two-dimensional Native-PAGE.

Bio-protocol (2018-07-05)
Marjaana Rantala, Virpi Paakkarinen, Eva-Mari Aro
ZUSAMMENFASSUNG

The hierarchical composition and interactions of the labile thylakoid protein complexes can be assessed by sequential 2D-native gel-electrophoresis system. Mild non-ionic detergent digitonin is used to solubilize labile protein super-and megacomplexes, which are then separated with first-dimension blue native polyacrylamide gel electrophoresis (1D-BN-PAGE). The digitonin derived protein complexes are further solubilized with stronger detergent, β-DM, and subsequently separated on an orthogonal 2D-BN-PAGE to release smaller protein subcomplexes from the higher-order supercomplexes. Here we describe a detailed method for 2D-BN-PAGE analysis of thylakoid protein complexes from Arabidopsis thaliana.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Trizma® Base, Primary Standard and Buffer, ≥99.9% (titration), crystalline
Sigma-Aldrich
Albumin aus Rinderserum, heat shock fraction, protease free, fatty acid free, essentially globulin free, pH 7, ≥98%
Sigma-Aldrich
Saccharose, for molecular biology, ≥99.5% (GC)
Millipore
Digitonin, hochrein, CAS 11024-24-1 is a non-ionic detergent commonly used to solubilize membrane-bound proteins.
Sigma-Aldrich
n-Dodecyl β-D-Maltosid, ≥98% (GC)
Sigma-Aldrich
Acrylamid, for molecular biology, ≥99% (HPLC)
Sigma-Aldrich
6-Amino-hexansäure, ≥99% (titration), powder