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Functional analysis of arabidopsis and rice vacuolar sorting receptor (VSR) proteins. / CUHK electronic theses & dissertations collection

Vacuolar sorting receptors (VSRs) are type I integral membrane family proteins that mediate protein transport from late Golgi or trans-Golgi network (TGN) to vacuole via prevacuolar compartment (PVC) in plant cells. The N-terminus of a VSR is believed to be important for cargo binding while its transmembrane domain (TMD) and cytoplasmic tail (CT) are essential for its correct subcellular localization. In this study, I first developed and tested an expression system using transgenic tobacco BY-2 cells to produce truncated VSR proteins (VSRNT) lacking the TMD/CT into the cultured media. The secreted VSRs bind specifically to the vacuolar sorting determinants (VSDs) of known vacuolar proteins and such binding is calcium dependent in vitro. Thus, VSR cargo proteins are likely secreted into the cultured media along with the truncated VSRs, which enable the identification of various VSR cargo proteins from the cultured media of transgenic cells. I then identified these putative VSR cargo proteins through liquid-chromatography with tandem mass spectrometry (LC-MS/MS) and Fourier transform mass spectrometry (FT-MS) using transgenic Arabidopsis cell suspension cultures PSB-D expressing these truncated VSRs. Among the 17 unique proteins found in the cultured media of transgenic Arabidopsis PSB-D cell line expressing VSRNT, an Arabidopsis glycosyl hydrolase family 3 protein At5g10560 (GH3) was chosen for further study on VSR-cargo protein interaction. GFP-tagged GH3 fusion protein was found to co-localize with VSR-RFP marker protein in PVC, whereas GH3 was also shown to interact with a VSR protein BP-80. Loss-of-function analysis demonstrated that the GH3 contained a vacuolar sorting determinant (VSD) for PVC targeting. / Suen, Pui Kit. / Source: Dissertation Abstracts International, Volume: 73-02, Section: B, page: . / Thesis (Ph.D.)--Chinese University of Hong Kong, 2010. / Includes bibliographical references (leaves 77-84). / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Electronic reproduction. [Ann Arbor, MI] : ProQuest Information and Learning, [201-] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Abstract also in Chinese.

Identiferoai:union.ndltd.org:cuhk.edu.hk/oai:cuhk-dr:cuhk_344711
Date January 2010
ContributorsSuen, Pui Kit., Chinese University of Hong Kong Graduate School. Division of Life Sciences.
Source SetsThe Chinese University of Hong Kong
LanguageEnglish, Chinese
Detected LanguageEnglish
TypeText, theses
Formatelectronic resource, microform, microfiche, 1 online resource (xi, 85 leaves : ill.)
RightsUse of this resource is governed by the terms and conditions of the Creative Commons “Attribution-NonCommercial-NoDerivatives 4.0 International” License (http://creativecommons.org/licenses/by-nc-nd/4.0/)

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