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How to picture the cell? |
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| Sep21-12, 07:49 AM | #52 |
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How to picture the cell?Whilst many molecules such as proteins have multiple roles they generally have very specific active sites. With regards to assembly look into chaperone proteins. |
| Sep21-12, 08:27 AM | #53 |
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Unfortunately my knowledge of biology is also extremely poor so it’s no surprise that my statements contradict what is already known. I would appreciate it very much if someone points out where I go wrong. |
| Sep21-12, 04:31 PM | #54 |
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One problem with the English is that you are excessively anthropomorphizing everything. For instance, you say that "all sorts of possibilities for chemical bonds seems like an obvious threat to order to me." Are the chemical bonds really threatening order? Is it obvious that the chemical bonds are threatening? Furthermore, you are "trying to imagine how diffusion can contribute to order." Did anyone say "diffusion is contributing to order"? You seem to think that diffusion is countering the threat of the possible chemical bonds. Maybe you are asking what reduces the probability of most chemical bonds forming, and why some chemical bonds are likely to form anyway. With that: In what are called living things, there are these large molecules with specific shapes. This simplified model is called "lock and key theory." The shape of the molecule makes certain chemical bonds unlikely to form after collision with other molecules. The shape of the molecule allows certain bonds to for after collision with other molecules. The selectivity is 80% of the time determined just by the geometry (shape) of the molecule. There are also electrical and magnetic forces involved. Quantum mechanics is also involved. What is important is that some chemical reactions are more likely than others for certain molecules. I will dump all these different properties into the word "shape". The randomness of the collision is greatly reduced by the shape and properties of the molecules. Now, maybe you want to know how the shape of the molecule got that way. The shape of each molecule is copied with high fidelity from generation to generation. However, high fidelity doesn't mean infinite fidelity. Some cells in each generation have a molecule or two which is slightly different. These are called inherited variations. Most mutations increase the probability of the cell dying or not reproducing in a certain environment. Some inherited variations improve the probability of the cell dying out in that environment. The cells with the improvements eventually outnumber the ones that remained the same or decreased the chance of survival. This is natural selection. Natural selection together with inherited variation supposedly determined the current shape of the molecules. Hypothetically, the molecules in the first generations of life did not have the specific shapes they had now. However, generation after generation of variation and selection has resulted in molecules of very specific shape. Now, what in my description can't you imagine? There was an article in the Washington Post on 20 September 2012 (Wedsday) in the Politics and Nation section. Some scientists kept a colony in a bacteria (E. coli) in bottle for 25 years. This corresponds to 50,000 generations of bacteria. The PI was Richard Lenski of Michigan State University. The full experiment is described in a recent issue of Nature. Alas, I don't have the original article in Nature. Every 500 generations, a sample from the colony was frozen as a record of changes. Some challenge was given every day to the flask. Every day, part of the colony was transferred to a new sugar solution. However, there was no exotic manipulation of the bacteria. The bacteria in the flask now have different molecules and different chemical reaction chains then their distant ancestors. The current bacteria now can digest citrate, something their distant ancestors could not do. This took about 30,000 generations of bacteria. Some of these chemical reaction chains seem very specific and rather complex. Yet at no time did any scientist "design" the molecules or reactions. The shape was not directly controlled except by providing that very general "challenge". There was no guidance to the shape. They just moved the bacteria into a new flask with fresh sugar every day. Yet, the new molecules have to have a really complex and specific shape to digest citrate. There are several other "unlikely" changes that have occurred over the 50,000 generations. Now, what do you think happened in that flask over 25 years and 50,000 generations? Please answer without anthropomorphizing anything. The E. coli may be insulted. |
| Sep21-12, 05:03 PM | #55 |
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http://www.ncbi.nlm.nih.gov/books/NBK26850/ http://www.ncbi.nlm.nih.gov/books/NBK26829/ http://en.wikipedia.org/wiki/Kinetic_proofreading |
| Sep21-12, 05:36 PM | #56 |
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But more importantly, your statement opposes the view that these sticky pieces can, indeed, through random motion, form functional structures. You have to remember the age of Earth and how many chances it's had to perform random trials. Even with legos, if you jumble them around in a box enough times, there is a chance they will eventually make some simple structures (even a car, though the chance is very very low). In none of these examples would you be able to commit enough trials in your lifetime... but life exceeds many lifetimes; billions of years of trials. It's not really surprising that all these sticky components had a chance to stick together in complicated ways. And remember that they didn't start out quite as complicated, it's been a very long period of emergence. There's a point at which early Earth chemistry becomes "life" through these small, random changes. Self-organized complexity. Here's a very simple example: notice that the system does require perturbation from time to time, but the perturbations for life would be found in the geophysics of the Earth (currents, heat vents, sun rising/setting, etc.). The only "order" is in the laws of physics that govern the particle interactions. All the other (macroscopic) "laws" are emergent and statistical in nature: they depend on the particular configuration of the ensemble of particles (including, in the above example, the red, blue, and bar magnets, the dish, and the water. For life, it could be the monomers, the heat vents, the lipid layer, and the ocean.) |
| Sep21-12, 05:47 PM | #57 |
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| Sep21-12, 06:02 PM | #58 |
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| Sep21-12, 06:26 PM | #59 |
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| Sep21-12, 06:46 PM | #60 |
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| Sep21-12, 07:10 PM | #61 |
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The statistics of "natural selection" can be said to support any balance there is, delicate or not. |
| Sep21-12, 07:13 PM | #62 |
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So to explain the ‘miracle’ of assembling by diffusion we need parts with specific shapes otherwise there is no 'falling into its right place'. This movie gives a very simple example of ‘falling into its right place’: Every part is falling into its right place. Unfortunately the parts in the movie all have the same shape which seems to contradict my reasoning. But I don’t think it does. I also think that there has to be a sequence in the assembling of the car. So highly specified part A must have just one right place B at moment C and highly specified part A’ must have just one right place B’ at moment C’ … etc. The parts in the cell are like pieces of an constantly changing puzzle. |
| Sep21-12, 08:17 PM | #63 |
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I'm also imaging a statespace bigger than just time; spatial correlation is just as important as temporal correlation. Sometimes 1/f dependency is happenstance too (as an over-simplified example, big waves travel further than little waves, so sampling ambient acoustics might yield pink noise, you'll be getting more global data in low frequencies and more local data in higher frequencies; once you adjust your system a posteriori for that bias, you have white noise again.) |
| Sep22-12, 02:20 AM | #64 |
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| Sep22-12, 10:39 AM | #65 |
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| Sep22-12, 12:04 PM | #66 |
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http://chemistry.caltech.edu/courses/ch110/lecture3.pdf |
| Sep22-12, 01:53 PM | #67 |
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Here's a paper (citaiton below) on this topic that you may be interested in taking a look at. The paper describes various chemical systems that mimic the self-assembly of the icosahedral poliovirus capsid. Of particular interest, the authors constructed a toy capsid that self assembles when shaken in a container: "By appropriate placement of oriented magnets as analogs to the electrostatic complementarity, we produced a model that mimics the self-assembly of the [poliovirus] from twelve pentameric assembly intermediates. Placing 12 of these tiles in a container and shaking with the appropriate strength results in a stable closed shell, usually within 1–2 min. The key aspects of this model were the fivefold symmetric tiles, the appropriate curvature at the tile interfaces, and the geometric and magnetic complementarity of the interfaces. Although intellectually we knew that this type of self-organization occurs spontaneously, watching it happen from random shaking on the macroscopic scale was inspirational."The videos of the process (freely available movie 1, and movie 2) are, as the authors say, inspirational. Movie 2 is especially impressive because it shows that two different capsids (colored red and green) with the same shapes but reversed magnet polarity can self-assemble in the presence of each other without the formation of misfolded states. So yes, you can put a collection of lego-like bricks in a tube, shake it up, and get a complex self-assembled structure. You can access the full paper at the PNAS website for free by following the link below: Olson, Hu, and Keinan. 2007. Chemical mimicry of viral capsid self-assembly. Proc. Natl. Acad. Sci. USA 104: 20731-20736. doi:10.1073/pnas.0709489104. On the topic of "delicate balance" and homeostasis, there is a good amount of scientific literature that has explored the effect of stochastic noise in protein and mRNA levels on the regulation of biological processes. I'll have to look up some good papers later, but Jonathan Weissman at UCSF and Erin O'Shea, formerly at UCSF now at Harvard, are two scientists who have done some of the key studies in this area. There's even an example of how bacteria take advantage of stochastic noise in order to produce pheotypic variability in a population of genetically identical cells (http://www.ncbi.nlm.nih.gov/pubmed/18927393). |
| Sep22-12, 02:08 PM | #68 |
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The point is simply that there's not a master control system guiding each process. In the context of previous posts by the OP (some of which have been deleted) there seems to be an agenda for strong emergence (not particularly creationism). Perhaps it's all a big misunderstanding, but it's not getting cleared up in the month it's been shrinking in growing in size as posts are deleted and reworded. What you seem to be proposing is weak emergence, which doesn't seem contradictory to my point. Whether you want to call consistent trends that emerge in the macroscopic world "laws" or not is not going to affect the science itself, it's just going to affect what aspects of the science you're emphasizing. So different research approaches are going to treat entropy differently. As long as we accept the map is not the territory, than we have to accept degeneracy between maps and territory. Some maps are going to describe different components differently. The strong emergence map doesn't tell you anything about the territory (except maybe hic sunt dracones). |
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