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Humana Press, Methods in Molecular Biology, p. 19-36, 2008

DOI: 10.1007/978-1-59745-028-7_2

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Purification and Proteomic Analysis of Chloroplasts and their Sub-Organellar Compartments.

Journal article published in 2008 by Daniel Salvi, Norbert Rolland, Jacques Joyard, Myriam Ferro
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

Sub-cellular proteomics has proven to be a powerful approach to link the information contained in sequenced genomes from eukaryotic cells to the functional knowledge provided by studies of cell compartments. Chloroplasts are plant-specific organelles and are the site of photosynthesis and also of many other essential metabolic pathways, like syntheses of amino acids, vitamins, and pigments. They contain several sub-organellar compartments: the envelope (the two-membrane system surrounding the organelle), the stroma (the internal soluble phase), and the thylakoid membranes (the internal membrane system). There is a link between these compartments and the functions of their constitutive proteins. One way to bring into view the sub-proteomes of the chloroplast is to develop proteomic analyses based (1) on the use of highly purified sub-fractions of the chloroplast and (2) on mass spectrometry (MS)-based analyses for protein identification. To illustrate such strategies, this chapter describes the methods for purification of chloroplasts from Arabidopsis leaves and for the specific recovery of highly pure sub-organellar fractions of envelope, stroma, and thylakoids. Subsequently, methods are described to analyze by MS the proteins recovered from these fractions.