Skip NavigationSkip to Content

A review of alternative promoters for optimal recombinant protein expression in baculovirus-infected insect cells

  1. Author:
    Grose,Carissa
    Putman,Zoe
    Esposito,Dom
  2. Author Address

    Frederick Natl Lab Canc Res, Prot Express Lab, NCI RAS Initiat, Canc Res Technol Program, Frederick, MD 21702 USA.
    1. Year: 2021
    2. Date: Oct
    3. Epub Date: 2021 06 01
  1. Journal: PROTEIN EXPRESSION AND PURIFICATION
  2. ACADEMIC PRESS INC ELSEVIER SCIENCE,
    1. 186
  3. Type of Article: Article
  4. Article Number: 105924
  5. ISSN: 1046-5928
  1. Abstract:

    Generating recombinant proteins in insect cells has been made possible via the use of the Baculovirus Expression Vector System (BEVS). Despite the success of many proteins via this platform, some targets remain a challenge due to issues such as cytopathic effects, the unpredictable nature of co-infection and co-expressions, and baculovirus genome instability. Many promoters have been assayed for the purpose of expressing diverse proteins in insect cells, and yet there remains a lack of implementation of those results when reviewing the landscape of commercially available baculovirus vectors. In advancing the platform to produce a greater variety of proteins and complexes, the development of such constructs cannot be avoided. A better understanding of viral gene regulation and promoter options including viral, synthetic, and insect-derived promoters will be beneficial to researchers looking to utilize BEVS by recruiting these intricate mechanisms of gene regulation for heterologous gene expression. Here we summarize some of the developments that could be utilized to improve the expression of recombinant proteins and multi-protein complexes in insect cells.

    See More

External Sources

  1. DOI: 10.1016/j.pep.2021.105924
  2. WOS: 000675885100002

Library Notes

  1. Fiscal Year: FY2020-2021
NCI at Frederick

You are leaving a government website.

This external link provides additional information that is consistent with the intended purpose of this site. The government cannot attest to the accuracy of a non-federal site.

Linking to a non-federal site does not constitute an endorsement by this institution or any of its employees of the sponsors or the information and products presented on the site. You will be subject to the destination site's privacy policy when you follow the link.

ContinueCancel