A novel method for viral display of ER membrane proteins on budded baculovirus |
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Authors: | Urano Yasuomi Yamaguchi Mineko Fukuda Rie Masuda Kazuyuki Takahashi Kazuaki Uchiyama Yasutoshi Iwanari Hiroko Jiang Shu-Ying Naito Makoto Kodama Tatsuhiko Hamakubo Takao |
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Institution: | Department of Molecular Biology, Research Center for Advanced Science and Technology, The University of Tokyo, #35 4-6-1 Komaba, Meguro, Tokyo 153-8904, Japan. |
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Abstract: | The baculovirus expression system has been used to express large quantities of various proteins, including membrane receptors. Here, we reveal a novel property of this expression system to be that certain membrane proteins can be displayed on the budded virus itself. We introduced the genes encoding sterol regulatory element-binding protein-2 (SREBP-2) or SREBP cleavage-activating protein (SCAP), important integral membrane proteins of the endoplasmic reticulum (ER) and/or the Golgi apparatus related to cellular cholesterol regulation, into a baculovirus vector. When insect cells were infected with SREBP-2 or SCAP recombinant viruses, it was found that these ER membrane proteins appeared on the budded baculovirus in addition to the host cell membrane fraction. Compared to proteins expressed on the cell membrane, membrane proteins displayed on virus exhibited both less aggregation and less degradation upon immunoblotting. Using this viral displayed SCAP as the screening antigen, we then generated a new monoclonal antibody specific against SCAP, which was useful for immunological localization studies. This system, which takes advantage of the viral display of membrane proteins, should prove to be a powerful additional tool for postgenomic protein analysis. |
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Keywords: | SREBP SCAP Endoplasmic reticulum Sf9 Baculovirus Budded virus Monoclonal antibody |
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