Basically you can (right now) fix protein part from one protein and hallucinate/design protein backbone backwards from it, using something like 4090, and that protein with high probability will fold as predicted. As an example fig. 3 in 2, shows you can design origami-like structures, which is not useful but very impressive, considering how long protein folding was dogshit despite compute power thrown into it.
Taking alphafold structures you can make proteins binding to other proteins, even without knowing nothing else, have appreciable expectation (>1 %) it will work. Which is how you can make designer viruses, if you were so inclined.
Drugs for now is not solved via neural networks, but they are working towards it, and i don’t see a reason why design of structures binding to known protein structures won’t work, it seems if anything else easier.
So, after taking some time to digest this information, I have a couple of follow-up questions, if you don’t mind answering them.
First of all, where do things stand with drugs? Is it just not something academics are working on, but presumably being done (or already finished) within proprietary institutions (e.g. Big Pharma)? Can you point me to some recent papers on the subject?
Secondly, what about enzymes? Binding proteins are interesting, certainly, but it’s enzymes that really excite me the most. Is anyone working on custom enzyme design, and if so, can you link some papers on that? In looking more closely at that Nature paper, I see that enzymes are something of a work-in-progress as yet. If you have anything else on the subject, I’d welcome that, but if there’s nothing else of note there, that’s fine.
Thank you for mentioning this to begin with, by the way, I really appreciate the info you’ve already shared!
With drugs third paper references it, i think in the next 6 months people expect neural net check of compounds binding affinities (https://www.biorxiv.org/content/10.1101/2023.11.01.565201v1.abstract), but here quantum chemistry is lagging behind, they still can’t do large molecules (>30 atoms) reliably. Basically rn the big bad boy is david baker lab, they do all this exciting stuff, you can periodically check google scholar for new developments like i do.
With enzymes (as i understand) the problem is to make them work, they can make them bind, but they can’t make them move to do stuff.
Alphafold can’t make conformations for now, and its a harder problem, so maybe in 2 years they can develop something reliable, as for now its mainly shenanigans of biasing folding programs into new conformations
https://www.science.org/doi/10.1126/science.add2187
https://www.nature.com/articles/s41586-023-06415-8
https://www.sciencedirect.com/science/article/abs/pii/S1476927122000445
Basically you can (right now) fix protein part from one protein and hallucinate/design protein backbone backwards from it, using something like 4090, and that protein with high probability will fold as predicted. As an example fig. 3 in 2, shows you can design origami-like structures, which is not useful but very impressive, considering how long protein folding was dogshit despite compute power thrown into it.
Taking alphafold structures you can make proteins binding to other proteins, even without knowing nothing else, have appreciable expectation (>1 %) it will work. Which is how you can make designer viruses, if you were so inclined.
Drugs for now is not solved via neural networks, but they are working towards it, and i don’t see a reason why design of structures binding to known protein structures won’t work, it seems if anything else easier.
Awesome, thanks!
So, after taking some time to digest this information, I have a couple of follow-up questions, if you don’t mind answering them.
First of all, where do things stand with drugs? Is it just not something academics are working on, but presumably being done (or already finished) within proprietary institutions (e.g. Big Pharma)? Can you point me to some recent papers on the subject?
Secondly, what about enzymes? Binding proteins are interesting, certainly, but it’s enzymes that really excite me the most. Is anyone working on custom enzyme design, and if so, can you link some papers on that?In looking more closely at that Nature paper, I see that enzymes are something of a work-in-progress as yet. If you have anything else on the subject, I’d welcome that, but if there’s nothing else of note there, that’s fine.Thank you for mentioning this to begin with, by the way, I really appreciate the info you’ve already shared!
With drugs third paper references it, i think in the next 6 months people expect neural net check of compounds binding affinities (https://www.biorxiv.org/content/10.1101/2023.11.01.565201v1.abstract), but here quantum chemistry is lagging behind, they still can’t do large molecules (>30 atoms) reliably. Basically rn the big bad boy is david baker lab, they do all this exciting stuff, you can periodically check google scholar for new developments like i do.
With enzymes (as i understand) the problem is to make them work, they can make them bind, but they can’t make them move to do stuff.
Alphafold can’t make conformations for now, and its a harder problem, so maybe in 2 years they can develop something reliable, as for now its mainly shenanigans of biasing folding programs into new conformations
This is great information, thank you so much!