共 30 条
BacMam system for high-level expression of recombinant soluble and membrane glycoproteins for structural studies
被引:105
作者:

Dukkipati, Abhirarn
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机构: Stanford Univ, Sch Med, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA

Park, Hyun Ho
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h-index: 0
机构: Stanford Univ, Sch Med, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA

Waghray, Deepa
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h-index: 0
机构: Stanford Univ, Sch Med, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA

Fischer, Suzanne
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h-index: 0
机构: Stanford Univ, Sch Med, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA

Garcia, K. Christopher
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h-index: 0
机构:
Stanford Univ, Sch Med, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA Stanford Univ, Sch Med, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA
机构:
[1] Stanford Univ, Sch Med, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA
关键词:
BacMam;
293;
cells;
GPCR;
Parathyroid hormone receptor;
Frizzled;
US28;
Chemokine;
Fractalkine;
Purification;
Crystallization;
D O I:
10.1016/j.pep.2008.08.004
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Baculovirus mediated gene transduction of mammalian cells (BacMam) is an emerging technique for rapid recombinant protein expression in mammalian cells. We constructed two baculovirus transfer vectors that incorporate several mammalian transcriptional regulatory elements necessary for high-level protein expression in mammalian cells. Using these vectors, we show that the BacMam system in combination with the 293 GnTI(-) cell line can be used for production of milligram quantities of soluble glycoproteins. Moreover, for crystallization trials, the purified glycoproteins are sensitive to EndoH treatment resulting in a loss of the bulk of the attached N-linked glycosylation. In addition, we also show that a combination of the BacMam system and 293 GnTI(-) cell line can be used for producing milligram quantities of a GPCR-protein ligand complex suitable for crystallization trials. (c) 2008 Elsevier Inc. All rights reserved.
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页码:160 / 170
页数:11
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