The international research team led
by the University of Leicester say the finding of HAP1 can bind to the
mutant huntingtin protein in proportion to the amount of aminoalkanoic
acids present in the glutamine repeat region. The subcellular location
of HAP1 closely resembles that of Htt. HAP1 interacts with alternative
factors concerned in sac trafficking as well as GABAA receptor, Rho-GEF,
and HGS.
HAP1 interacts with muHtt in a very
polyQ dependent manner. Its localization and doable interacting
partners have since been characterized, so elucidating a doable role for
this protein in HD pathological process. HAP1 is localized in mitotic
spindle of dividing striatal cells, such as endosomes, microtubules and
vesicles in the basal neural structure and striatial neurons, where
HAP1B is preferentially expressed.
The role of HAP1(www.bioabb.com/products/Human-Huntingtin%252dassociated-protein-1%28HAP1%29-ELISA-kit.html)
in HD pathological process could involve aberration of cell cycle
processes, as high immunostaining of HAP1 throughout the cell cycle has
been ascertained. HAP1 can also disrupt endocytosis, as it has been
detected on vesicles concerned within the early stages of this method.
It's doable that the non-pathogenic activity of HAP1 is living thing
trafficking which this is often rattled following its association with
mHtt. HAP1 interacts with proteins aside from Htt and it's possible that
their perform is altered in HD pathological process. These embody
dynactin p150Glued, a living substance dynein accent protein concerned
in retrograde transport of organelles, and kinesin-like protein that is
another transport-mediation protein.
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