Fluorescence protease protection of GFP chimeras to reveal protein topology and subcellular localization
- 17 February 2006
- journal article
- research article
- Published by Springer Nature in Nature Methods
- Vol. 3 (3) , 205-210
- https://doi.org/10.1038/nmeth857
Abstract
Understanding the cell biology of many proteins requires knowledge of their in vivo topological distribution. Here we describe a new fluorescence-based technique, fluorescence protease protection (FPP), for investigating the topology of proteins and for localizing protein subpopulations within the complex environment of the living cell. In the FPP assay, adapted from biochemical protease protection assays, GFP fusion proteins are used as noninvasive tools to obtain details of protein topology and localization within living cells in a rapid and straightforward manner. To demonstrate the broad applicability of FPP, we used the technique to define the topology of proteins localized to a wide range of organelles including the endoplasmic reticulum (ER), Golgi apparatus, mitochondria, peroxisomes and autophagosomes. The success of the FPP assay in characterizing the topology of the tested proteins within their appropriate compartments suggests this technique has wide applicability in studying protein topology and localization within the cell.Keywords
This publication has 32 references indexed in Scilit:
- Suppression of chaperone-mediated autophagy in the renal cortex during acute diabetes mellitusKidney International, 2004
- Global analysis of protein localization in budding yeastNature, 2003
- Cellular Phenotyping of Secretory and Nuclear Prion Proteins Associated with Inherited Prion DiseasesJournal of Biological Chemistry, 2002
- A Novel Method to Determine the Topology of Peroxisomal Membrane Proteins in Vivo Using the Tobacco Etch Virus ProteasePublished by Elsevier ,2001
- LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processingThe EMBO Journal, 2000
- The Reversible Modification Regulates the Membrane-Binding State of Apg8/Aut7 Essential for Autophagy and the Cytoplasm to Vacuole Targeting PathwayThe Journal of cell biology, 2000
- Identification and characterization of the human peroxin PEX3European Journal of Cell Biology, 1999
- Chimeric green fluorescent protein as a tool for visualizing subcellular organelles in living cellsCurrent Biology, 1995
- Green Fluorescent Protein as a Marker for Gene ExpressionScience, 1994
- Transmembrane topology of acetylcholine receptor subunits probed with photoreactive phospholipidsBiochemistry, 1985