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Differential proteomic analysis of the endoplasmic reticulum from developing and germinating seeds of castor ( Ricinus communis ) identifies seed protein precursors as significant components of the endoplasmic reticulum
Author(s) -
Maltman Daniel J.,
Gadd Stephen M.,
Simon William J.,
Slabas Antoni R.
Publication year - 2007
Publication title -
proteomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.26
H-Index - 167
eISSN - 1615-9861
pISSN - 1615-9853
DOI - 10.1002/pmic.200600694
Subject(s) - ricinus , endoplasmic reticulum , storage protein , germination , biochemistry , biology , protein biosynthesis , proteome , microbiology and biotechnology , biosynthesis , botany , enzyme , gene
The endoplasmic reticulum is a major compartment of storage protein and lipid biosynthesis. Maximal synthesis of these storage compounds occurs during seed development with breakdown occurring during germination. In this study, we have isolated four independent preparations of ER from both developing and germinating seeds of castor bean ( Ricinus communis ) and used 2‐D DIGE, and a combination of PMF and MS/MS sequencing, to quantify and identify differences in protein complement at both stages. Ninety protein spots in the developing seeds are up‐regulated and 19 individual proteins were identified, the majority of these are intermediates of seed storage synthesis and protein folding. The detection of these transitory storage proteins in the ER is discussed in terms of protein trafficking and processing. In germinating seed ER 15 spots are elevated, 5 of which were identified, amongst them was malate synthetase which is a component of the glyoxysome which is believed to originate from the ER. Notably no proteins involved in complex lipid biosynthesis were identified in the urea soluble ER fraction indicating that they are probably all integral membrane proteins.