IBM takes first 3D image of atomic bonds
gizmodo.com
gizmodo.com
It should be noted that this sort of resolution has been attainable for some time using scanning tunneling microscopy, but I'm pretty sure this is a first for atomic force microscopy. STM doesn't give you a very good image of bonds -- in fact bonds are generally the thing you _don't_ see, since STM works by pulling electrons in/out and bonds are stable places where electrons really don't want to come out of or go into. AFM, on the other hand, shows bonds very nicely.
You can sorta make out where the aromatic rings are. I'm not sure why it's so bright at the ends -- any organic chemists out there who can explain that?
Also, consider that an electron is 1/1000 the size of a proton.
Despite the common image, electrons don't orbit the nucleus like planets around the sun. They sort of exist around the entire thing in all locations at the same time (in 3D, not in a ring, but a shell).
i'm hoping the guy was being sarcastic but...
Molecules have no color because they are smaller then the shortest length wave of light you and I can see.
Think about dropping a stone in a quiet pond. Think of the waves that are created. If they bump into a large obstacle they are reflected back. If they hit a tiny one, like a thin blade of grass sticking out of the water, they just flow around.
Gold is golden because a whole lot of gold atoms bunched together reflect a yellowish range of light. Gold the material is gold colored. A single gold atom does not have color.
It seems to me it's an argument about semantics, not physics.
A single atom has very specific set of electron energies as a consequence of the electrons being confined to the area around the nucleus. This means that it can only absorb or emit photons with energies corresponding to the spacings between any two energy levels (and the absorption/emission must be accompanied by a jump/fall of an electron between corresponding energy levels. Any type of atom will thus have a secific pattern of absorption/emission peaks, this is incidentally how we can tell the composition of stars and dust clouds in distant galaxies.
For a lump of metal, a good approximation is to consider the electrons as being able to freely roam throughout the entire crystal. As a consequence, when they are excited by an incoming photon (of any energy), they immediately relax back to their original state, emitting the photon again at the same energy. This is why metal films act as mirrors and why metals in general are shiny. As for the goldish color of Gold, that has to do with some relativistic effects which I don't understand (yet ;-) ). I believe the same is true for Copper.
(I may make this question a separate post to HN, it's been bothering me for a while.)
A simple example (the names are removed to make this easier to digest, but if you're curious it's the action of Glyceraldehyde-3-Phosphate Dehydrogenase in glycolysis) involves a protein which is known to play a part in the breakdown of glucose. This protein catalyzes the addition of a "high energy" phosphate to our compound so we can break it down further while also pulling off a reactive hydrogen (and adding it to NAD+ to make NADH) so the cell can use that later (another kind of energy like ATP).
Biochemists, assuming they can already purify the compound and know the overall reaction, investigated the action of the enzyme by mixing in a highly reactive fluorescent-tagged molecule that looks similar to the product of the reaction. This molecule bound permanently to the inside of the enzyme which was then denatured and sequenced, looking for whatever amino acid showed the fluorescent tag (cysteine). Then the inserted modified reagents which contained radioactive hydrogen and phosphate to figure out where exactly those molecules ended up. In this way they learned where the enzyme added the phosphate to the product and exactly which hydrogen was removed from the initial compound to make that NADH.
Biochemistry is a really fascinating story of minute triumphs of discovery. Unfortunately, like any part of science like that, it means that the day-to-day life of a biochemist is backbreaking and tedious. Regardless, if you're interesting, there is a lot of fun stuff to study.
Not being able to see (and as the toothpick -> truck of floss poster mentioned above, this isn't going to help with biological systems much at this point) does mean there are significant gaps in what biologists know. On the other hand, biologists have been visualizing larger structures for some time (even proteins via xray etc.)
It's depressing to consider the fact that it would probably get downvoted on the science subreddit.
So, now that we can 'see' the 3D arrangement in a manner of speaking is there any way we could feed known protein structure in to neural networks by imaging them in quantity and take some of the sting out of protein folding by identifying likely candidate ways to do the folding ?
Or is that too big of a leap ?
It's a kind of the opposite approach: instead of slowly collecting information from extremely static scene they will blast the sample with very powerful X-ray laser, taking snapshot before shattering it to pieces.
http://www.xfel.eu/en/research-examples/structure-of-biomole...
Not to piss on a parade, but I don't see this as major breakthrough. It's a technical achievement with an established technology, of primary benefit to material scientists and nanotechnologists, both of whom already have imaging techniques at this level, but lack easy, cheap and instant ones, and face most of their hurdles at the design and synthesis side, not imaging/proof of construct
From a biochemist's point of view, if it was anywhere near real-time, THAT would be awesome.
What he said. This is amazing.
I guess the fact this book comes with pictures probably gives it an edge there.
Pentacene on flickr - http://www.flickr.com/photos/ibm_research_zurich/3839799374/
IBM Research Zurich (pix of lab) - http://www.flickr.com/photos/ibm_research_zurich/
Article in MIT Tech Review - http://www.technologyreview.com/blog/editors/24040/
"The imaging work is described today in the journal Science."
Fun search result on www.sciencemag.org for ibm+zurich
Science 10 July 1987 - 'IBM's Zurich Lab Is "Flower" in Europe: Two major discoveries—the scanning tunneling microscope and superconducting ceramics—highlight IBM Zurich lab's success in tapping Europe's scientific talent'
Cut them some slack. At least they're watching/trying. Their article is a news item here, after all.
They're trying? Trying what? What they usually do is copy-paste from the source. That does not add much value. Hence, I ask again: where's the URL to the original press release? I don't want to read such great news from a website that allows comments from retards who know nothing about Physics...
Call me elitist if you will. BTW, my question was rhetorical.