Subcellular localization of legionella Dot/Icm effectors


Autoria(s): Vogrin, Adam J; Mousnier, Aurelie; Frankel, Gad; Hartland, Elizabeth L
Data(s)

2013

Resumo

<p>The translocation of effector proteins by the Dot/Icm type IV secretion system is central to the ability of Legionella pneumophila to persist and replicate within eukaryotic cells. The subcellular localization of translocated Dot/Icm proteins in host cells provides insight into their function. Through co-staining with host cell markers, effector proteins may be localized to specific subcellular compartments and membranes, which frequently reflects their host cell target and mechanism of action. In this chapter, we describe protocols to (1) localize effector proteins within cells by ectopic expression using green fluorescent protein fusions and (2) localize effector proteins within infected cells using epitope-tagged effector proteins and immuno-fluorescence microscopy.</p>

Identificador

http://pure.qub.ac.uk/portal/en/publications/subcellular-localization-of-legionella-doticm-effectors(a93d6f89-5c87-4e17-b7b8-882a3693b9b8).html

http://dx.doi.org/10.1007/978-1-62703-161-5_20

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Vogrin , A J , Mousnier , A , Frankel , G & Hartland , E L 2013 , ' Subcellular localization of legionella Dot/Icm effectors ' Methods in Molecular Biology , vol 954 , pp. 333-44 . DOI: 10.1007/978-1-62703-161-5_20

Palavras-Chave #Bacterial Proteins #Bacterial Secretion Systems #Cloning, Molecular #Gene Expression #Green Fluorescent Proteins #HEK293 Cells #Humans #Legionella #Legionella pneumophila #Microscopy, Fluorescence #Plasmids #Protein Transport #Recombinant Fusion Proteins #Transfection
Tipo

article