Recent comments in /f/science

bane_killgrind t1_j9e4d6k wrote

So this concept of chirality isn't adequately explained, so I'm going to give a shot at that.

Most of the visualizations we have of molecules are flat, and so they offer an incomplete picture of how they exist in real life and the texture they have. Some long molecule is likely to be bent or rotated along certain bonds because of the individual charges of the atomic components that it's made up by.

Some forces attract, and other forces repel, a position that balances those forces could be straight or very bendy.

Let's pretend a sheet of paper is some molecule. It has a side A and a side B. The stiff surface of the paper offers an internal repelling force and the edges have an attractive force. If you cut a triangle out of the sheet, (a different shape is a different molecule) the attraction in the edges pulls the cutout into a cone. But now we need to ask, is side A the outside of the cone or is side B? It could be either, and the way to describe this distinction between two otherwise identical molecules is it's chirality.

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blackluck64 t1_j9e418z wrote

In time the entire planet will exist to support just one species. We'll end up killing off most of our only companions on possibly the only inhabitable planet for complex life in the galaxy. And most people seem just fine with that.

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basmwklz OP t1_j9e2xnv wrote

Abstract: >Accumulation of misfolded protein aggregates is a hallmark event in many age-related protein misfolding disorders, including some of the most prevalent and insidious neurodegenerative diseases. Misfolded protein aggregates produce progressive cell damage, organ dysfunction, and clinical changes, which are common also in natural aging. Thus, we hypothesized that aging is associated to the widespread and progressive misfolding and aggregation of many proteins in various tissues. In this study, we analyzed whether proteins misfold, aggregate, and accumulate during normal aging in three different biological systems, namely senescent cells, Caenorhabditis elegans, and mouse tissues collected at different times from youth to old age. Our results show a significant accumulation of misfolded protein aggregates in aged samples as compared to young materials. Indeed, aged samples have between 1.3 and 2.5-fold (depending on the biological system) higher amount of insoluble proteins than young samples. These insoluble proteins exhibit the typical characteristics of disease-associated aggregates, including insolubility in detergents, protease resistance, and staining with amyloid-binding dye as well as accumulation in aggresomes. We identified the main proteins accumulating in the aging brain using proteomic studies. These results show that the aged brain contain large amounts of misfolded and likely non-functional species of many proteins, whose soluble versions participate in cellular pathways that play fundamental roles in preserving basic functions, such as protein quality control, synapsis, and metabolism. Our findings reveal a putative role for protein misfolding and aggregation in aging.

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Welcome to r/science! This is a heavily moderated subreddit in order to keep the discussion on science. However, we recognize that many people want to discuss how they feel the research relates to their own personal lives, so to give people a space to do that, personal anecdotes are allowed as responses to this comment. Any anecdotal comments elsewhere in the discussion will be removed and our normal comment rules apply to all other comments.

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ddlbot t1_j9dyrn1 wrote

me too, i asked ChatGPT to summarize it...

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The article discusses the challenges of quantifying ultrastructural features of pleomorphic organelles in three dimensions using cellular cryo-electron tomography (cryo-ET) and proposes a semiautomated workflow to segment organellar membranes and reconstruct their underlying surface geometry in cryo-ET. The authors also developed an open-source suite of ultrastructural quantifications, integrated into a single pipeline called the surface morphometrics pipeline, which enables rapid modeling of complex membrane structures and allows detailed mapping of inter- and intramembrane spacing, curvedness, and orientation. The authors demonstrate the advantages of this approach by combining cryo-ET with cryo-fluorescence microscopy to correlate bulk mitochondrial network morphology with membrane ultrastructure of individual mitochondria in the presence and absence of endoplasmic reticulum (ER) stress. Using their pipeline, the authors demonstrate ER stress promotes adaptive remodeling of ultrastructural features of mitochondria and suggest that changes in membrane ultrastructure correlate to mitochondrial network morphologies. Overall, the pipeline offers opportunities for quantifying changes in membrane ultrastructure on a single-cell level using cryo-ET, opening new opportunities to define changes in ultrastructural features induced by diverse types of cellular perturbations

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so i said "Explain like i'm Five"

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>Scientists want to see how tiny parts inside cells look like in 3D to understand how cells work. They use a fancy machine called cryo-electron tomography (cryo-ET) to take pictures of these tiny parts. But it's hard to understand what the pictures mean. So, the scientists came up with a way to make the pictures easier to understand. They made a computer program that helps them to see the parts better and to compare them with other cells. They used this program to study mitochondria, tiny parts that make energy for cells. They found that when cells are stressed, mitochondria change their shape and structure to adapt to the stress. They hope that this program will help them learn more about how cells work and how they respond to different conditions.

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Gotanyfunkopops t1_j9dyok1 wrote

My wife is a physician and we have tested frequently for it since the onset, and nope, neither of us have caught it. My wife is super careful, even now she still wears face shields and N95. I work from home and we still wear masks when we go out, so that helps too. We actually haven’t been sick with cold or flu in three years either.

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laveshnk t1_j9dwsja wrote

My uncle had a similar stroke in his early fiftys. He was this wonderful old man who could only move his finger, so we attached a bell to his wheelchair arm. Unfortunately he was killed in a bomblast in his very own nursing home.

I can still remember sound of the dings he used to make.

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