HR-Bac, a toolbox based on homologous recombination for expression, screening and production of multiprotein complexes using the baculovirus expression system

Olga Kolesnikova, Amélie Zachayus, Simon Pichard, Judit Osz, Natacha Rochel, Paola Rossolillo, Isabelle Kolb-Cheynel, Nathalie Troffer-Charlier, Emmanuel Compe, Olivier Bensaude, Imre Berger, Arnaud Poterszman*

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

7 Citations (Scopus)
61 Downloads (Pure)

Abstract

The Baculovirus/insect cell expression system is a powerful technology for reconstitution of eukaryotic macromolecular assemblies. Most multigene expression platforms rely on Tn7-mediated transposition for transferring the expression cassette into the baculoviral genome. This allows a rigorous characterization of recombinant bacmids but involves multiple steps, a limitation when many constructs are to be tested. For parallel expression screening and potential high throughput applications, we have established an open source multigene-expression toolbox exploiting homologous recombination, thus reducing the recombinant baculovirus generation to a single-step procedure and shortening the time from cloning to protein production to 2 weeks. The HR-bac toolbox is composed of a set of engineered bacmids expressing a fluorescent marker to monitor virus propagation and a library of transfer vectors. They contain single or dual expression cassettes bearing different affinity tags and their design facilitates the mix and match utilization of expression units from Multibac constructs. The overall cost of virus generation with HR-bac toolbox is relatively low as the preparation of linearized baculoviral DNA only requires standard reagents. Various multiprotein assemblies (nuclear hormone receptor heterodimers, the P-TEFb or the ternary CAK kinase complex associated with the XPD TFIIH subunit) are used as model systems to validate the toolbox presented.

Original languageEnglish
Article number2030
Number of pages12
JournalScientific Reports
Volume12
Issue number1
DOIs
Publication statusPublished - 7 Feb 2022

Bibliographical note

Funding Information:
We thank I Jones for the generous gift of the AcMNPV bacmid and Arthur Vogt for help with the characterization of the virus pool. We acknowledge support from the Institut National de la Santé et de la Recherche Médicale (INSERM), the Centre National pour la Recherche Scientifique (CNRS), the Ligue contre le Cancer, the Institut National du Cancer (INCA_9378 (2015-142)), ANR-12-BSV8-0015-01, ANR-20-CE12-0017 and ANR-10-LABX-0030-INRT, a French State fund managed by the Agence Nationale de la Recherche under the frame program Investissements d’Avenir ANR-10- IDEX-0002-02. We acknowledge the use of resources of the French Infrastructure for Integrated Structural Biology FRISBI ANR-10-INBS-05, of Instruct-ERIC (RD project funding) and of Instruct-ULTRA as part of the European Union’s Horizon 2020 (grant ID 731005).

Publisher Copyright:
© 2022, The Author(s).

Research Groups and Themes

  • Bristol BioDesign Institute

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