Purification of Protein-complexes from the Cyanobacterium Synechocystis sp. PCC 6803 Using FLAG-affinity Chromatography

0534703 - MBÚ 2021 RIV US eng J - Journal Article
Koskela, Minna M. - Skotnicová, Petra - Sobotka, Roman
Purification of Protein-complexes from the Cyanobacterium Synechocystis sp. PCC 6803 Using FLAG-affinity Chromatography.
Bio-protocol. Roč. 10, č. 10 (2020), č. článku e3616. ISSN 2331-8325
R&D Projects: GA ČR(CZ) GA17-08755S; GA MŠMT(CZ) LO1416
Institutional support: RVO:61388971
Keywords : Protein purification * Membrane protein complexes * Synechocystis 6803 * Photosystems
OECD category: Microbiology
Method of publishing: Limited access
https://en.bio-protocol.org/e3616

Exploring the structure and function of protein complexes requires their isolation in the native state-a task that is made challenging when studying labile and/or low abundant complexes. The difficulties in preparing membrane-protein complexes are especially notorious. The cyanobacterium Synechocystis sp. PCC 6803 is a widely used model organism for the physiology of oxygenic phototrophs, and the biogenesis of membrane-bound photosynthetic complexes has traditionally been studied using this cyanobacterium. In a typical approach, the protein complexes are purified with a combination of His-affinity chromatography and a size-based fractionation method such as gradient ultracentrifugation and/or native electrophoresis. However, His-affinity purification harbors prominent contaminants and the levels of many proteins are too low for a feasible multi-step purification. Here, we have developed a purification method for the isolation of 3x FLAG-tagged proteins from the membrane and soluble fractions of Synechocystis. Soluble proteins or solubilized thylakoids are subjected to a single affinity purification step that utilizes the highly specific binding of FLAG-affinity resin. After an intensive wash, the captured proteins are released from the resin under native conditions using an excess of synthetic 3x FLAG peptide. The protocol allows fast isolation of low abundant protein complexes with a superb purity.
Permanent Link: http://hdl.handle.net/11104/0312872