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An in vivo expression system for the identification of cargo proteins of vacuolar sorting receptors in A rabidopsis culture cells
Author(s) -
Shen Jinbo,
Suen Pui Kit,
Wang Xiangfeng,
Lin Youshun,
Lo Sze Wan,
Rojo Enrique,
Jiang Liwen
Publication year - 2013
Publication title -
the plant journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.058
H-Index - 269
eISSN - 1365-313X
pISSN - 0960-7412
DOI - 10.1111/tpj.12257
Subject(s) - microbiology and biotechnology , protein targeting , secretion , biology , in vivo , receptor , protein sorting signals , transport protein , cell culture , membrane protein , computational biology , gene , signal peptide , biochemistry , genetics , recombinant dna , membrane
Summary Vacuolar sorting receptors ( VSR s) are type I integral membrane family proteins that in plant cells are thought to recognize cargo proteins at the late G olgi or trans ‐ G olgi network ( TGN ) for vacuolar transport via the pre‐vacuolar compartment ( PVC ). However, little is known about VSR cargo proteins in plants. Here we developed and tested an in vivo expression system for the identification of VSR cargos which is based on the premise that the expressed N ‐terminus of VSR s will be secreted into the culture medium along with their corresponding cargo proteins. Indeed, transgenic A rabidopsis culture cell lines expressing VSR N‐terminal binding domains (VSRNTs) were shown to secrete truncated VSR s ( BP 80 NT , At VSR 1 NT and At VSR 4 NT ) with attached cargo molecules into the culture medium. Putative cargo proteins were identified through mass spectrometry. Several identified cargo proteins were confirmed by localization studies and interaction analysis with VSR s. The screening strategy described here should be applicable to all VSR s and will help identify and study cargo proteins for individual VSR proteins. This method should be useful for both cargo identification and protein–protein interaction in vivo .