MultiBac: multigene baculovirus-based eukaryotic protein complex production
- PMID: 18429060
- DOI: 10.1002/0471140864.ps0520s51
MultiBac: multigene baculovirus-based eukaryotic protein complex production
Abstract
Multiprotein complexes are an emerging focus in current biology, resulting in a demand for advanced heterologous expression systems. This unit provides protocols for the expression of eukaryotic multiprotein complexes using multigene expression vectors. Homologous and site-specific recombinases facilitate their assembly. Thus, modification of individual subunits for revised expression studies is achieved with comparative ease. The strategy outlined here employs the MultiBac baculoviral expression system for multiprotein complexes as an example. Baculoviral expression does not require particular safety precautions due to the replication incompetence of baculovirus in mammalian hosts. The MultiBac system provides for improved protein production due to deletion of specific viral genes (V-cath, chiA). Most of the steps described in this unit are tailored for high-throughput approaches. The general strategy of rapidly combining encoding DNAs by recombination into multigene expression vectors for protein complex expression can also be applied to other prokaryotic or mammalian expression systems.
(c) 2008 by John Wiley & Sons, Inc.
Similar articles
-
Protein complex expression by using multigene baculoviral vectors.Nat Methods. 2006 Dec;3(12):1021-32. doi: 10.1038/nmeth983. Nat Methods. 2006. PMID: 17117155
-
New baculovirus expression tools for recombinant protein complex production.J Struct Biol. 2010 Oct;172(1):45-54. doi: 10.1016/j.jsb.2010.02.010. Epub 2010 Feb 21. J Struct Biol. 2010. PMID: 20178849
-
MultiBac: Baculovirus-Mediated Multigene DNA Cargo Delivery in Insect and Mammalian Cells.Viruses. 2019 Feb 26;11(3):198. doi: 10.3390/v11030198. Viruses. 2019. PMID: 30813511 Free PMC article. Review.
-
Baculovirus expression system for heterologous multiprotein complexes.Nat Biotechnol. 2004 Dec;22(12):1583-7. doi: 10.1038/nbt1036. Epub 2004 Nov 28. Nat Biotechnol. 2004. PMID: 15568020
-
The MultiBac Baculovirus/Insect Cell Expression Vector System for Producing Complex Protein Biologics.Adv Exp Med Biol. 2016;896:199-215. doi: 10.1007/978-3-319-27216-0_13. Adv Exp Med Biol. 2016. PMID: 27165327 Free PMC article. Review.
Cited by
-
MultiBacMam Bimolecular Fluorescence Complementation (BiFC) tool-kit identifies new small-molecule inhibitors of the CDK5-p25 protein-protein interaction (PPI).Sci Rep. 2018 Mar 23;8(1):5083. doi: 10.1038/s41598-018-23516-x. Sci Rep. 2018. PMID: 29572554 Free PMC article.
-
Evolution of fungal tuberculosis necrotizing toxin (TNT) domain-containing enzymes reveals divergent adaptations to enhance NAD cleavage.Protein Sci. 2024 Jul;33(7):e5071. doi: 10.1002/pro.5071. Protein Sci. 2024. PMID: 38895984 Free PMC article.
-
Expression and purification of human neutrophil proteinase 3 from insect cells and characterization of ligand binding.PLoS One. 2024 Jun 25;19(6):e0294827. doi: 10.1371/journal.pone.0294827. eCollection 2024. PLoS One. 2024. PMID: 38917138 Free PMC article.
-
The Cac2 subunit is essential for productive histone binding and nucleosome assembly in CAF-1.Sci Rep. 2017 Apr 18;7:46274. doi: 10.1038/srep46274. Sci Rep. 2017. PMID: 28418026 Free PMC article.
-
Structure of transmembrane prolyl 4-hydroxylase reveals unique organization of EF and dioxygenase domains.J Biol Chem. 2021 Jan-Jun;296:100197. doi: 10.1074/jbc.RA120.016542. Epub 2020 Dec 20. J Biol Chem. 2021. PMID: 33334883 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources