Features Partner Sites Information LinkXpress hp
Sign In
Advertise with Us
INTEGRA BIOSCIENCES AG

Download Mobile App




Crystal Structure Reveals How Neutralizing Antibody Blocks Astrovirus Infection

By Gerald M. Slutzky, PhD
Posted on 08 Dec 2016
A team of molecular virologists used X-ray crystallography to establish how a neutralizing antibody bound to the surface of the gastroenteritis-causing astrovirus and blocked its entry into uninfected cells.

Human astroviruses (HAstVs) are a leading cause of viral diarrhea in young children, the immune compromised, and the elderly. More...
There are no vaccines or antiviral therapies against HAstV disease. Several lines of evidence point to the presence of protective antibodies in healthy adults as a mechanism governing protection against reinfection by HAstV. However, development of anti-HAstV therapies has been hampered by the gap in knowledge of protective antibody epitopes on the HAstV capsid surface.

To better understand how neutralizing antibodies bind to HAstV, investigators at the University of California, Santa Cruz (USA) used X-ray crystallography to examine the structure of the HAstV capsid spike domain bound to the neutralizing monoclonal antibody PL-2.

The investigators reported in the November 2, 2016, online edition of the Journal of Virology that the antibody used all six complement-determining regions to bind to a quaternary epitope on each side of the dimeric capsid spike. Furthermore, the investigators determined that the HAstV capsid spike was a receptor-binding domain and that the antibody neutralized HAstV by blocking virus attachment to cells.

These findings suggested that a subunit-based vaccine focusing the immune system on the HAstV capsid spike domain could be effective in protecting children against HAstV disease.

"We have identified a site of vulnerability on the surface of the virus that we can now target for development of a vaccine or antiviral therapy," said senior author Dr. Rebecca DuBois, assistant professor of biomolecular engineering at the University of California, Santa Cruz. "These are the first results showing how a neutralizing antibody blocks this virus. Antibody therapeutics is a rapidly growing field. Many immunotherapies are being developed to target cancer cells, and we expect to see a growing number of antibody therapies for infectious diseases over the next ten years."

Related Links:
University of California, Santa Cruz


New
Gold Member
Nucleic Acid Extractor System
NEOS-96 XT
POC Helicobacter Pylori Test Kit
Hepy Urease Test
New
Japanese Encephalitis Test
Japanese Encephalitis Virus Real Time PCR Kit
New
CMV CLIA Diagnostic
CLIA CMV IgA Screen Group
Read the full article by registering today, it's FREE! It's Free!
Register now for FREE to LabMedica.com and get access to news and events that shape the world of Clinical Laboratory Medicine.
  • Free digital version edition of LabMedica International sent by email on regular basis
  • Free print version of LabMedica International magazine (available only outside USA and Canada).
  • Free and unlimited access to back issues of LabMedica International in digital format
  • Free LabMedica International Newsletter sent every week containing the latest news
  • Free breaking news sent via email
  • Free access to Events Calendar
  • Free access to LinkXpress new product services
  • REGISTRATION IS FREE AND EASY!
Click here to Register








Channels

Immunology

view channel
Image: Accurate immunotherapy selection for esophageal and GEJ carcinomas depends on consistent PD-L1 assessment (credit: Adobe Stock)

FDA Approval Expands Use of PD-L1 Companion Diagnostic in Esophageal and GEJ Carcinomas

Esophageal and gastroesophageal junction carcinomas (GEJ) have a poor prognosis, with approximately 16,250 deaths in the United States in 2025 and a five-year relative survival of 21.9%.... Read more
Copyright © 2000-2026 Globetech Media. All rights reserved.