Garry Nolan's role with the CCR5 receptor. Garr
Post# of 155581
Garry Nolan is the Rachford and Carlota A. Harris Professor in the Department of Pathology at the Stanford University School of Medicine.
He also holds a joint appointment in the Department of Microbiology and Immunology.
Why do we care?
In my original post, the entertaining YouTube interview of Nolan urges us to make him a Leronlimab ally.
https://www.youtube.com/watch?v=HxVVz2Jorzk
Gary Nolan, among his various research endeavors,
[ ] has contributed to our understanding of the CCR5 receptor, primarily in the context of its role as an HIV-1 co-receptor.
His research focused on
[ ] How the CCR5 receptor facilitates HIV-1 entry into cells.
[ ] Along with CD4, CCR5 is used by HIV-1 to enter cells like macrophages and T cells.
To investigate this mechanism, Nolan and his team studied
[ ] The role of CCR5's signal transduction.
[ ] The team introduced mutations in the cytoplasmic domains of CCR5,
[ ] including truncating the carboxyl-tail and mutating the DRY sequence.
[ ] These mutations blocked chemokine-dependent activation of second messengers like intracellular calcium fluxes and chemotaxis.
[ ] However, these mutations did not affect CCR5's function as an HIV-1 co-receptor.
[ ] This led to the conclusion that signal transduction, a typical function of G protein-coupled receptors like CCR5, is not necessary for CCR5 to act as an HIV-1 co-receptor.
In essence, Nolan's work demonstrated that
[ ] HIV can utilize CCR5 for entry even when the receptor's usual signaling functions are inhibited .
[ ] This finding is significant for understanding HIV-1 entry and may contribute to developing new therapies.

