Gene gymnastics Synthetic biology for baculovirus expression vector system engineering
被引:32
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作者:
Vijayachandran, Lakshmi S.
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机构:
UJF EMBL CNRS, EMBL, Grenoble Outstn, UMR 5233, Grenoble, France
UJF EMBL CNRS, UVHCI, UMR 5233, Grenoble, FranceUJF EMBL CNRS, EMBL, Grenoble Outstn, UMR 5233, Grenoble, France
Vijayachandran, Lakshmi S.
[1
,2
]
Raj, Deepak B. Thimiri Govinda
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h-index: 0
机构:
UJF EMBL CNRS, EMBL, Grenoble Outstn, UMR 5233, Grenoble, France
UJF EMBL CNRS, UVHCI, UMR 5233, Grenoble, FranceUJF EMBL CNRS, EMBL, Grenoble Outstn, UMR 5233, Grenoble, France
Raj, Deepak B. Thimiri Govinda
[1
,2
]
Edelweiss, Evelina
论文数: 0引用数: 0
h-index: 0
机构:
UJF EMBL CNRS, EMBL, Grenoble Outstn, UMR 5233, Grenoble, France
UJF EMBL CNRS, UVHCI, UMR 5233, Grenoble, France
UMR5075 CEA CNRS Univ Joseph Fourier, IBS, Grenoble, FranceUJF EMBL CNRS, EMBL, Grenoble Outstn, UMR 5233, Grenoble, France
Edelweiss, Evelina
[1
,2
,3
]
Gupta, Kapil
论文数: 0引用数: 0
h-index: 0
机构:
UJF EMBL CNRS, EMBL, Grenoble Outstn, UMR 5233, Grenoble, France
UJF EMBL CNRS, UVHCI, UMR 5233, Grenoble, FranceUJF EMBL CNRS, EMBL, Grenoble Outstn, UMR 5233, Grenoble, France
Gupta, Kapil
[1
,2
]
Maier, Josef
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h-index: 0
机构:
Informat Serv Life Sci IStLS, Oberndorf, GermanyUJF EMBL CNRS, EMBL, Grenoble Outstn, UMR 5233, Grenoble, France
Maier, Josef
[4
]
论文数: 引用数:
h-index:
机构:
Gordeliy, Valentin
[3
]
Fitzgerald, Daniel J.
论文数: 0引用数: 0
h-index: 0
机构:
Geneva Biotech, Geneva, SwitzerlandUJF EMBL CNRS, EMBL, Grenoble Outstn, UMR 5233, Grenoble, France
Fitzgerald, Daniel J.
[5
]
Berger, Imre
论文数: 0引用数: 0
h-index: 0
机构:
UJF EMBL CNRS, EMBL, Grenoble Outstn, UMR 5233, Grenoble, France
UJF EMBL CNRS, UVHCI, UMR 5233, Grenoble, FranceUJF EMBL CNRS, EMBL, Grenoble Outstn, UMR 5233, Grenoble, France
Berger, Imre
[1
,2
]
机构:
[1] UJF EMBL CNRS, EMBL, Grenoble Outstn, UMR 5233, Grenoble, France
[2] UJF EMBL CNRS, UVHCI, UMR 5233, Grenoble, France
[3] UMR5075 CEA CNRS Univ Joseph Fourier, IBS, Grenoble, France
[4] Informat Serv Life Sci IStLS, Oberndorf, Germany
Most essential activities in eukaryotic cells are catalyzed by large multiprotein assemblies containing up to ten or more interlocking subunits. The vast majority of these protein complexes are not easily accessible for high resolution studies aimed at unlocking their mechanisms, due to their low cellular abundance and high heterogeneity. Recombinant overproduction can resolve this bottleneck and baculovirus expression vector systems (BEVS) have emerged as particularly powerful tools for the provision of eukaryotic multiprotein complexes in high quality and quantity. Recently, synthetic biology approaches have begun to make their mark in improving existing BEVS reagents by de novo design of streamlined transfer plasmids and by engineering the baculovirus genome. Here we present OmniBac, comprising new custom designed reagents that further facilitate the integration of heterologous genes into the baculovirus genome for multiprotein expression. Based on comparative genome analysis and data mining, we herein present a blueprint to custom design and engineer the entire baculovirus genome for optimized production properties using a bottom-up synthetic biology approach.