This is the first plain English description of Cailyn's genetic anomaly that I've ever seen.
STXBP1 and the bubble bath.
In order to understand the 
function of STXBP1, just imagine a bubble bath (on Sunday evenings, our 
little daughter usually has a bath, therefore, this example was obvious 
to me). Imagine two medium-sized bubbles floating on the water. What 
does it take to turn these two bubbles into one big bubble? Yes, it is 
quite difficult. The more you try to push them together, the more you 
risk generating many small bubbles rather than a single big one. For soap bubbles,
 this task is a bit easier, but also here you will end up with a burst 
bubble rather than a single big bubble in many cases. In terms of 
(bio)physics, the joining of bubbles is a matter of overcoming the 
repulsive forces when joining two lipid bilayers,
 i.e. it’s not natural for bubbles to join, you have to give them a 
push. To cut a long story short, why is this relevant for the human 
brain? Our synapses have the same problem thousands of times each 
millisecond. In order to enable synaptic transmission, we need to fuse 
synaptic vesicles. Each of these vesicles needs a little push to fuse 
with the presynaptic membrane. And STXBP1 is one of proteins providing 
this push.
1 comment:
That actually makes sense. I read the rest of the post... and it makes my head spin. ((hugs)) to you and the whole family.
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