Yea, that's correct. Though I may probably omit proteins and large moelcules, requiring transport vesicles and any specific transport mechanisms.
Stochasticity sounds like there has been performed some theoretical modelling to infer this. But does it imply that there would be some tiny % of any ligand molecules - endogenous or exogenous - which would just by chance get "an empty run" and didn't bind to their receptors (though structurally they're fine ligands with high affinity) and would be removed via waste removal systems? Is there any experimental evidence for this, like some study using radiolabelled high affinity ligand molecules to see what % of them gets into "an empty run"?
The mean free path seems sort of sensible in the extracellular space, though it still seems that the variables affecting mean free path (large amounts of receptors and binding thingys, the very small spaces, and the temperature) may be not enough. But wouldn't mean free path be near zero inside cells, where every nanometer should be occupied by some other biochemical pathway/reaction or bioelectric activity?
>>Neither you nor I will see biology as a mature science.
I personally wouldn't care a lot about proving anything to anybody in some absolute sense, but first of all to prove instrumentally and make stuff work for myself at least. I think that any biology student with the descent understanding should have some mini lab for personalized medicine (as e.g. Sinclair mentioned that his recent research on using 6 chemical compounds for OSK epigenetic reprogramming (rather than bulky viral vectors) can be done by any biology student).
Oh yes, many studies on unused targets/receptors are out there. It's a very common thing in the cell. Sure, yes, there are a lot of transport mechanisms to get the higher Dalton things about. But, again, it's all kinda random down there. Look at a lot of synapse regulation and you'll see that signaling molecules will escape the cleft and have to be digested. There's this really fun 'dance' that astrocytes do to regulate damaged NMDA receptors (and likely all receptors) that kinda makes the synapse just spill out all the signaling compounds for a little while. The cilia in neurons will also act as a kind of passive radar for a cell, just taking in signals and seeing what is going on with all the unused stuff floating about.
The mean free path is pretty much 0 all over, so to speak. I was just trying to tie it back into more EE concepts for you. The idea is that things are just randomly moving about, with a 'free' mean free path, until they aren't, and that stoppage costs energy. At body temperatures, it doesn't take much to knock binding ligands out of a cleft. So the stiffer the bind, the harder to disassociate, and the harder to get it to unbind at the end. Nature kinda figures this all out on her own, and the optimal energies are found out via evolution. It's all a 'good enough' system.
So, the trick with bio is that it's a lot like how Clausewitz thinks of war: War is easy, it's just that all the easy stuff is really hard. In that, it's conceptually easy to do bio. It's just that it's really hard to implement anything. Feynman talked a bit about it in one of his lectures. In that, getting a rat to randomly go into a room and then discover that there is cheese in it will take a tremendous amount of prep and careful cleaning and the like. Rats have really really good noses. It's so easy to fool yourself in bio, because the systems are just so complicated. And, for me, that's been true up and down the size scale, from single cells to whole animals. The systems are just so complex, you really only get to ask simple questions and then hope you controlled the experiment correctly.
All the empirical examples you mentioned pertain to the extracellullar space. So is this stochastic modelling also true in the intracellular space, which is like 100x times denser structurally, biochemically and bioelectrically (given that all biochemistry is effectively a type of electrical process involving very refined transfer/manipulations of charge densities), and allows to explain how do hundreds or thousands of biochemical reaction inside cells happen as required without interfering with each other?
Evolution also "tries" to save energy anywhere possible, so spending energy on the synthesis of endogenous ligands, which eventually will be discarded, seems a bit redundant. There is also a theorem in evolutionary game theory, that probability that natural selection will allow an organism to see reality as it is (=the truth) is exactly zero, as it's enough to make it just "good enough". I was arguing about that with Gemini, and it agreed with me. My point is that "evolution" is just a tool (like ChatGPT) with it's own instrumentally limited pool of empirical data (80% of which was also obtained from macroscopic enough observations rather than reverse engineering or experimentation) to build upon.
I actually want to apply one EE concept, which has some experimental basis. The reason why I am digging this, is that I am searching for some possible explanations of a couple of dozens of experimental studies in bioelectrics/magnetics I found. (though won't discuss in depth on a public forum)
I mean, how is the intracellular space denser than the extracellular? That means they wouldn't float.
The stochastic nature of the cell, as far as I know, exists pretty much the same in and out. With more transport mechanims occurring inside to make sure things get to where they need to be.
It's not that the discarded ligands (for example) are really 'discarded'. There are a few instances I know of that use the 'waste' as a product unto themselves. The ToR network comes to mind here. Still, trying to really figure out what the 'intention' was all those billions of years ago is hard, and networks and feedback loops have been built up over the eons. Like, yeah, nothing is really wasted in a cell, per se. But it can seem that way in the chain that you're looking at.
I'd love to know more about the magnetic side of things here. Is it memristors as synapses? Because that is a criminally misunderstood area of neuroscience.
>>how is the intracellular space denser than the extracellular?
Gemini:
```
Yes, the intracellular space is denser than the extracellular space:
Here's why:
Packing: Cells are packed with molecules like proteins, carbohydrates, and nucleic acids. These molecules take up a significant amount of space within the cell, leaving little room for just water.
Solutes: The intracellular space contains a higher concentration of dissolved molecules (solutes) compared to the extracellular space. This contributes to a higher density.
Extracellular Matrix: The extracellular space, on the other hand, contains a looser network of connective tissues and fluids like interstitial fluid. This allows for more space between molecules, resulting in a lower density.
```
>>Still, trying to really figure out what the 'intention' was all those billions of years ago is hard
With this logic you'll need another billion of years to randomly figure it out. I'd rather focus on how/efficiently does such position contribute to a specific current experimental methodology or results.
Yeah, sure cell densities vary (fat vs muscle) but pretty much any cell sample you're going to gather is going to be near the same density as the surrounding water environment. Again, there is a lot of variation though. The end result is that the density of a cell is near enough the density of water, it's not 100x more dense. I mean, iron is only ~8x more dense than water.
100x was a demo, not an actual number. But please explain how does intracellular content with DNA, RNA, proteins, structural organoids and all of these metabolic constituents [0] is supposed to be the density of water. You want the cells in an endotelium of a blood vessel to float, allow the blood to get into the wall of the vessel and get hematomas and hemmorhages?
Thank you so much for your explanations - I have learned a lot. I have some more questions but also have about 40 tabs of papers and terms to digest first, and I think the thread will probably go stale by then. May I ask what you studied and how you came into this type of knowledge from an engineering background, and whether you'd recommend any recent texts to come up to date on this stuff with?
I did a career change from particle physics to bioengineering and neuroscience ( and now AI/ML for EE applications with bioreactors, but that's another story).
There's not a lot of recent texts really. US based academia in the last few years has been really bad, as the replication crisis turned into a dry cough; I.E. make up data all you want, no one will care.
I'd really recommend reading Darwin though. Going way back to the literal foundation really helps set the stage, mentally, and bring you back to what is really going on with relation to the wider human condition.
Just about any review article more than 10 years old is also going to be pretty good. I'd stay way from review articles less than 5 years old though, as things change and retractions come out.
I'll warn you though, the concepts and mental models that you've built up on the Engineering side are not really going to help you with the bio side. Yes, the study habits will help. But bio is really really complicated. You can't abstract the cow into a meter sphere of water. In bio, you really do care about that cell on the medial side of the fourth mesenchymal layer of the second stomach of the cow. You are going to have to get comfortable memorizing pathways and strange names for a few years before all the pieces will even start fitting together. Again, bio is something that's been surviving, ripping, and gouging, for ~4 billion years. She don't have time to stop and let us know what is up.
In parallel with Darwin also try more recent advancements,like Don Hoffman's "The case against reality", where they prove that the probability that evolution will equip an organism to see the true reality is Zero.
Stochasticity sounds like there has been performed some theoretical modelling to infer this. But does it imply that there would be some tiny % of any ligand molecules - endogenous or exogenous - which would just by chance get "an empty run" and didn't bind to their receptors (though structurally they're fine ligands with high affinity) and would be removed via waste removal systems? Is there any experimental evidence for this, like some study using radiolabelled high affinity ligand molecules to see what % of them gets into "an empty run"?
The mean free path seems sort of sensible in the extracellular space, though it still seems that the variables affecting mean free path (large amounts of receptors and binding thingys, the very small spaces, and the temperature) may be not enough. But wouldn't mean free path be near zero inside cells, where every nanometer should be occupied by some other biochemical pathway/reaction or bioelectric activity?
>>Neither you nor I will see biology as a mature science.
I personally wouldn't care a lot about proving anything to anybody in some absolute sense, but first of all to prove instrumentally and make stuff work for myself at least. I think that any biology student with the descent understanding should have some mini lab for personalized medicine (as e.g. Sinclair mentioned that his recent research on using 6 chemical compounds for OSK epigenetic reprogramming (rather than bulky viral vectors) can be done by any biology student).