A protein folding mystery solved: Study explains core packing fractions

phys.org

94 points by PaulHoule 5 days ago


gilleain - 3 days ago

The 'explanation' in the article is a little thin:

Why is the packing fraction 55% maximum (in globular proteins)? "The answer seems to be that the packing fraction stops increasing when the protein cores jam or rigidify." Ok, so ...

> "That is, the individual amino acids that make up the protein core couldn't compress any further when the protein folded"

So they can't pack any further because they 'jam'? Ohhh, from the abstract of the paper:

> "... However, important developments in the physics of jamming in particulate systems can shed light on the packing of protein cores. ... Then, we develop an all-atom model for proteins and find that, above ∼0.55, protein cores undergo a jamming-like transition"

Possibly this is related to the need for protein cores to remain relatively 'liquid', as enzymes (for example) need to be somewhat flexible when binding/releasing substrates. A fully 'jammed'/packed core would lead to an inflexible structure with lower ability to ... er... move, bind stuff (I'm handwaving here :) )

ChuckMcM - 3 days ago

This is the kind of cool stuff I'm going to miss during the coming dark ages. When ever I read this in a paper:

"The authors acknowledge support from NIH Training Grant No. T32GM145452 (A.T.G., C.S.O., and Z.L.), NIH Training Grant No. T15LM007056-37 (J.A.L.), and the High Performance Computing facilities operated by Yale's Center for Research Computing."

All of these things (the NIH and Yale's Center for Research Computing) relied so heavily on government funding that they are no longer getting, especially if they don't sing ideologically pure songs for dear Leader.

pfdietz - 3 days ago

"In living organisms, every protein—a type of biological polymer consisting of hundreds of amino acids—carries out specific functions, such as catalysis, molecule transport, or DNA repair. To perform these functions, they must fold up into specific shapes."

This is not true. There are some proteins that are intrinsically disordered, not folding into any preferred way, but they still perform biological functions.

https://en.wikipedia.org/wiki/Intrinsically_disordered_prote...

timdellinger - 3 days ago

for perspective, monodisperse spheres max out at 74% (hexagonal close packing)

SamSeeder - 3 days ago

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banq - 3 days ago

The research direction has gone off track—it's overly fixated on proteins "chasing fireworks" (metaphorically trivial pursuits), while mitochondrial and other molecular pathways represent a far more substantial and impactful frontier. The academic world is mired in stagnation and decay, demanding external pressure to break its complacency.