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

A high efficiency cloning and expression system for proteomic analysis.

Xuan Z Ding1, Ian T Paulsen, Apurba K Bhattacharjee

  • 1Department of Bacterial Diseases, Division of Communicable Diseases and Immunology, Walter Reed Army Institute of Reseach, Silver Spring, MD 20910-7500, USA. tom.ding@na.amedd.army.mil

Proteomics
|June 27, 2006
PubMed
Summary
This summary is machine-generated.

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

Calciphylaxis complicated by NDM-1-producing Pseudomonas aeruginosa: first experience with cefepime-zidebactam alongside phage therapy in the USA.

The Lancet. Infectious diseases·2026
Same author

One Yeast, Sixteen Synthetic Chromosomes, Infinite Possibilities.

Yeast (Chichester, England)·2026
Same author

Genome sequences of 19 <i>Klebsiella</i> phages of the genus <i>Przondovirus</i>.

Microbiology resource announcements·2026
Same author

Synthesis of Programmable Bioelectronic Yeast for Biohybrid Futures.

Engineering biology·2026
Same author

Environment and Pollen Diversity Differentially Affect the Gut Microbiomes of Introduced Honeybees and Bumblebees.

Evolutionary applications·2026
Same author

Agriculture alters protein evolution of respiratory nitrate reductase in soil bacteria at a global scale.

Environmental research·2026

Researchers developed a high-efficiency cloning and expression system (HECES) for Brucella proteins. This system aids in identifying new diagnostic reagents and vaccine candidates for brucellosis, a significant zoonotic disease.

Area of Science:

  • Microbiology
  • Immunology
  • Genomics

Background:

  • Brucella species are major zoonotic pathogens and biothreat agents.
  • Complete genome sequences of pathogenic Brucella are now available.
  • Antigenicity analysis of Brucella proteins is crucial for diagnostics and vaccines.

Purpose of the Study:

  • To develop a high-efficiency cloning and expression system (HECES) for Brucella proteins.
  • To enable genome-based analysis of Brucella protein antigenicity.
  • To facilitate the selection of new diagnostic reagents and vaccine candidates for brucellosis.

Main Methods:

  • A bench-level high-efficiency cloning and expression system (HECES) was established.
  • Large numbers of Brucella proteins were expressed based on genomic sequence information.

Related Experiment Videos

  • Purified proteins were produced in a microarray format for sero-reactivity analysis.
  • Main Results:

    • The HECES demonstrated high efficiency in protein production.
    • The microarray format allowed for efficient analysis of protein sero-reactivity.
    • The system is scalable from small to large-scale protein processing.

    Conclusions:

    • The HECES provides a powerful tool for analyzing Brucella protein antigenicity.
    • This method supports the development of novel reagents for brucellosis diagnosis.
    • The system facilitates the creation of effective vaccines against Brucella infections.