Sign In  |  Register  |  About San Rafael  |  Contact Us

San Rafael, CA
September 01, 2020 1:37pm
7-Day Forecast | Traffic
  • Search Hotels in San Rafael

  • CHECK-IN:
  • CHECK-OUT:
  • ROOMS:

Creative Biolabs: Summarizing Malaria Infection Mechanisms and Introducing Biotherapeutic Discovery

By: Get News
Creative Biolabs introduced the discovery of biomolecular approaches targeting Plasmodium, aiming to assist academia and the pharmaceutical industry in relieving the malaria health crisis.

New York, USA - January 4, 2024 - Malaria remains a global health threat, causing millions of cases and hundreds of thousands of deaths each year. Plasmodium falciparum, the most lethal of the malaria parasites affecting humans, has long been a formidable adversary in the quest for effective antimalarial treatments. Creative Biolabs has long been dedicated to discovering innovative solutions to combat this deadly infectious disease. A resource essay entitled "The Evolutionary Mechanisms of Hijacking IgM in Plasmodium falciparum" was published on the company's website lately, summarizing a recent research paper in Nature Communications that reports on the complicated molecular mechanisms of P. falciparum proteins hijacking IgM and introducing its biomolecular discovery services to facilitate parasitic disease research and therapeutic development.

"The sound research results indicate that antibodies, especially IgM, comprise the first line of defense to neutralize pathogens," according to a scientist at Creative Biolabs. "We've collected IgM antibodies that can serve as an instrument to study the intricate dance between Plasmodium and the host's immune system. In the meantime, we have also constructed the AntInfectâ„¢ platform to facilitate the discovery of anti-bacteria biomolecular."

The high-throughput AntInfectâ„¢ integrates antigen-specific B lymphocyte cytometry technology to construct a comprehensive list of premade peptide libraries, hybridoma and phage display technologies for anti-parasite antibody screening, and phage display based epitope mapping to cover the miscellaneous research pursuits and to back the discovery of biomolecular targeting plasmodium, of which the main targets and their underlying mechanisms are:

* Apical membrane antigen 1 (AMA1): to inhibit the interaction between AMA1 and rhoptry neck protein 2 (RON2)

* Erythrocyte binding antigen-175 (EBA-175): to prevent EBA-175 and glycophorin A (GpA) binding event

* P. falciparum Reticulocyte Binding Protein Homologue 5 (PfRH5): to prohibit PfRH5 from interacting with its receptor Basigin (BSG)

"Thanks to this breakthrough discovery that sheds light on the mechanisms of how this parasite impairs IgM's neutralizing ability," said the scientist, "the attempts towards conquering Malaria become more straightforward, with researchers concentrating more on these straight-to-the-point therapeutic targets."

As Creative Biolabs continues to push the boundaries of scientific exploration, the company invites collaboration with research institutions, pharmaceutical partners, and other stakeholders to accelerate the translation of these findings into tangible therapeutic solutions.

For more information, please visit https://www.creative-biolabs.com/antinfect.

About

Creative Biolabs is a leading biotechnology company dedicated to providing innovative solutions in the fields of drug discovery, antibody development, and custom services. With a commitment to excellence and a focus on advancing precision medicine, Creative Biolabs leverages cutting-edge technologies to address the most challenging scientific questions.

Media Contact
Company Name: Creative Biolabs
Contact Person: Candy Swift
Email: Send Email
Phone: 1-631-830-6441
Country: United States
Website: https://www.creative-biolabs.com



Data & News supplied by www.cloudquote.io
Stock quotes supplied by Barchart
Quotes delayed at least 20 minutes.
By accessing this page, you agree to the following
Privacy Policy and Terms and Conditions.
 
 
Copyright © 2010-2020 SanRafael.com & California Media Partners, LLC. All rights reserved.