Cost-Effective Manufacturing of Human Quality mRNA

Information

  • Research Project
  • 6737144
  • ApplicationId
    6737144
  • Core Project Number
    R43GM070156
  • Full Project Number
    1R43GM070156-01
  • Serial Number
    70156
  • FOA Number
  • Sub Project Id
  • Project Start Date
    1/1/2004 - 20 years ago
  • Project End Date
    6/30/2004 - 20 years ago
  • Program Officer Name
    FEINGOLD, ELISE A
  • Budget Start Date
    1/1/2004 - 20 years ago
  • Budget End Date
    6/30/2004 - 20 years ago
  • Fiscal Year
    2004
  • Support Year
    1
  • Suffix
  • Award Notice Date
    12/22/2003 - 20 years ago
Organizations

Cost-Effective Manufacturing of Human Quality mRNA

DESCRIPTION (provided by applicant): The overall objective of this proposal is to develop methods for the cost-effective, large-scale synthesis (up to kilograms amounts) of capped RNA. Companies such as Wyeth Vaccines, AlphaVax and Merix Biosciences are using capped RNA to produce human vaccines against cancers and infectious diseases such as HIV and biowarfare agents. The mMESSAGEmMACHINE(r) kit, based on Ambion's patented technology, provides the customer with high-yielding transcription reactions for the synthesis of capped RNA. Although this technology is the best available on the market for producing capped RNA, the cost of making capped RNA using this technology under cGMP conditions may be too cost prohibitive to make these RNA-based vaccine strategies commercially feasible. Additionally, the current technology produces a mixture of uncapped, correctly capped and "reverse" capped RNA. Our goals are to decrease the cost of the capped RNA required per human subject by at least 100-fold, to increase the purity of the capped RNA such that >90% of the RNA is correctly capped and to develop methods for assessing the purity of the final RNA product. By developing a new reaction system, we could theoretically increase the yield of these reactions by as much a 8-fold. Preliminary experiments increased the yield up to 3-fold based on this novel strategy. By increasing the ratio of the cap analog to GTP concentrations in these reaction systems, we should be able to increase the percentage of capped RNA in a reaction to 90% and further, by using a novel "anti-reverse cap analog" we will incorporate all of the cap in the correct, functional orientation. Increasing the resistance of the capped RNA to nucleases is one strategy to decrease the amount of RNA required per human subject and we will test various strategies for increasing the stability of the capped RNA in a cell while maintaining its translational competency. Finally, not all of the transcription components required for generating maximum yields are available as an FDA approved component. These proteins will be cloned and expressed in systems approved by the FDA.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R43
  • Administering IC
    GM
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    122108
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    821
  • Ed Inst. Type
  • Funding ICs
    NIGMS:122108\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    AMBION, INC.
  • Organization Department
  • Organization DUNS
    198680068
  • Organization City
    AUSTIN
  • Organization State
    TX
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    787441832
  • Organization District
    UNITED STATES