🦴 Could a naturally occurring “biological lubricant” redefine how we treat joint health and gout?

🔗 Lubricin’s Mucin Domain Has Strong Polyproline Type II Helical Character. Computational and Structural Biotechnology Journal (CSBJ). DOI: https://doi.org/10.34133/csbj.0021

📚 CSBJ - A Science Partner Journal: https://spj.science.org/journal/csbj

#StructuralBiology #ProteinScience #Biophysics #ComputationalBiology #Osteoarthritis #Glycoproteins #MolecularBiology

Posting on behalf of the @ncfg -

In our latest Interesting Fact Post learn about Mitochondrial Glycoproteins!
Think #mitochondria don't have #glycoproteins? Think again! New research shows O-GlcNAc modifications are key to: Energy Brain Health, Development

Read: https://research.bidmc.org/ncfg/blog/25-facts-about-mitochondrial-glycoproteins

#Glycobiology #glycotime

25] Facts About: Mitochondrial Glycoproteins

National Center for Functional Glycomics (NCFG)

💡 Have you ever wondered how many N-Glycans or #glycoproteins there are on cells?

The numbers are massive: calculations suggest about 20 to 200 million N-glycans per human cell!

Read the full blog post: https://research.bidmc.org/ncfg/blog/24-facts-about-number-glycoproteins-and-n-glycans-cell

#glycobiology #glycotime #cells #biology

Comparative Characterization of #Bronchial and #Nasal #Mucus Reveals Key #Determinants of #Influenza A Virus #Inhibition http://biorxiv.org/cgi/content/short/2024.09.17.613498v1?rss=1

The ability of mucus to neutralize influenza A virus varies with the anatomical origin of the #airway cultures and correlates with the abundance of #triglycerides and sialylated #glycoproteins and #glycolipids.

#Adaptation potential of #H3N8 canine #influenza virus in #human respiratory #cells, Sci Rep.: https://www.nature.com/articles/s41598-024-69509-x

We found that CIV acquired high growth properties in these cells mainly through #mutations in surface #glycoproteins, such as hemagglutinin (#HA) and neuraminidase (#NA). Our reverse genetics approach revealed that HA2-K82E, HA2-R163K, and NA-S18L mutations were responsible for the increased growth of CIV in human cells.

Adaptation potential of H3N8 canine influenza virus in human respiratory cells - Scientific Reports

In 2004, the equine-origin H3N8 canine influenza virus (CIV) first caused an outbreak with lethal cases in racing greyhounds in Florida, USA, and then spread to domestic dogs nationwide. Although transmission of this canine virus to humans has not been reported, it is important to evaluate its zoonotic potential because of the high contact opportunities between companion dogs and humans. To gain insight into the interspecies transmissibility of H3N8 CIV, we tested its adaptability to human respiratory A549 cells through successive passages. We found that CIV acquired high growth properties in these cells mainly through mutations in surface glycoproteins, such as hemagglutinin (HA) and neuraminidase (NA). Our reverse genetics approach revealed that HA2-K82E, HA2-R163K, and NA-S18L mutations were responsible for the increased growth of CIV in human cells. Molecular analyses revealed that both HA2 mutations altered the optimum pH for HA membrane fusion activity and that the NA mutation changed the HA-NA functional balance. These findings suggest that H3N8 CIV could evolve into a human pathogen with pandemic potential through a small number of mutations, thereby posing a threat to public health in the future.

Nature