Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

PROfusion: genetically tagged proteins for functional proteomics and beyond.

B L Kreider1

  • 1Phylos, Inc., 128 Spring Street, Lexington, MA 02421, USA.

Medicinal Research Reviews
|May 8, 2000
PubMed
Summary

Phylos, Inc. developed PROfusion technology, linking proteins to their mRNA for large-scale functional genomics. This enables the selection of proteins with desired functions from massive synthetic and natural libraries.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

In vitro selection and characterization of Bcl-X(L)-binding proteins from a mix of tissue-specific mRNA display libraries.

The Journal of biological chemistry·2001
Same author

Dendritic cells and MPIF-1: chemotactic activity and inhibition of endogenous chemokine production by IFN-gamma and CD40 ligation.

Journal of leukocyte biology·1999
Same author

STRL22 is a receptor for the CC chemokine MIP-3alpha.

Biochemical and biophysical research communications·1997
Same author

Molecular and functional characterization of two novel human C-C chemokines as inhibitors of two distinct classes of myeloid progenitors.

The Journal of experimental medicine·1997
Same author

The Evi-1 zinc finger myeloid transforming protein binds to genomic fragments containing (GATA)n sequences.

Oncogene·1995
Same author

Interleukin-3 signals through multiple isoforms of Stat5.

The EMBO journal·1995

Area of Science:

  • Functional genomics
  • Molecular biology
  • Biotechnology

Background:

  • Protein function discovery is crucial for understanding biological processes.
  • Existing methods for library construction have limitations in scale and efficiency.
  • A need exists for novel technologies to create and screen large protein libraries.

Purpose of the Study:

  • To introduce and describe the PROfusion technology for protein-mRNA tagging.
  • To demonstrate the construction of large synthetic and natural protein libraries using this technology.
  • To highlight the utility of PROfusion technology for selecting proteins based on function.

Main Methods:

  • Development of PROfusion technology for covalent protein-mRNA tagging.
  • Construction of synthetic and natural protein libraries in vitro.

Related Experiment Videos

  • Selection of proteins with specific functions from large libraries.
  • Utilizing linked mRNA for PCR amplification and identification.
  • Main Results:

    • PROfusion technology enables direct linkage of proteins to their genetic information (mRNA).
    • Creation of exceptionally large libraries, up to 10^14 molecules.
    • Demonstrated capability to select proteins based on desired functions.
    • Facilitated subsequent PCR amplification and identification of selected proteins.

    Conclusions:

    • PROfusion technology is a powerful new tool for functional genomics.
    • The ability to construct massive libraries significantly advances protein discovery.
    • This technology streamlines the process of identifying functional proteins for various applications.