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Science

Adding New DNA Letters Make Novel Proteins Possible (economist.com) 102

An anonymous reader quotes a report from The Economist: The fuzzy specks growing on discs of jelly in Floyd Romesberg's lab at Scripps Research in La Jolla look much like any other culture of E. coli. But appearances deceive -- for the dna of these bacteria is written in an alphabet that has six chemical letters instead of the usual four. Every other organism on Earth relies on a quartet of genetic bases: a (adenine), c (cytosine), t (thymine) and g (guanine). These fit together in pairs inside a double-stranded dna molecule, a matching t and c, g. But in 2014 Dr Romesberg announced that he had synthesised a new, unnatural, base pair, dubbed x and y, and slipped them into the genome of E. coli as well. Kept supplied with sufficient quantities of X and Y, the new cells faithfully replicated the enhanced DNA -- and, crucially, their descendants continued to do so, too. Since then, Dr Romesberg and his colleagues have been encouraging their new, "semisynthetic" cells to use the expanded alphabet to make proteins that could not previously have existed, and which might have properties that are both novel and useful. Now they think they have found one. In collaboration with a spin-off firm called Synthorx, they hope to create a less toxic and more effective version of a cancer drug called interleukin-2.

Interleukin-2 works by binding to, and stimulating the activity of, immune-system cells called lymphocytes. The receptor it attaches itself to on a lymphocyte's surface is made of three units: alpha, beta and gamma. Immune cells with all three form a strong bond to interleukin-2, and it is this which triggers the toxic effect. If interleukin-2 can be induced to bind only to the beta and gamma units, however, the toxicity goes away. And that, experiments have shown, can be done by attaching polyethylene glycol (PEG) molecules to it. The trick is to make the PEGs stick. This is where the extended genetic alphabet comes in. Using it, Synthorx has created versions of interleukin-2 to which PEGs attach themselves spontaneously in just the right place to stop them linking to the alpha unit. Tested on mice, the modified molecule has exactly the desired anti-tumor effects. Synthorx plans to ask permission for human trials later this year.

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Adding New DNA Letters Make Novel Proteins Possible

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  • Genetically-improved E. coli.

  • Z! (Score:4, Insightful)

    by ChatHuant ( 801522 ) on Thursday January 17, 2019 @08:07PM (#57980088)

    Do you want World War Z?! Because that's how you get World War Z!

    • Re:Z! (Score:5, Funny)

      by PPH ( 736903 ) on Thursday January 17, 2019 @08:45PM (#57980226)

      This is also how you get Leeloo. I'm OK with this.

      • by Anonymous Coward

        Multipass!

      • So you're into oddly-unattractive androgynous orangeheads.

        It's all good; some people still eat their boogers...

        • lol, look, a neckbeard who is frightened and confused by a woman with an athletic figure!

          There are a bunch of kids in the next tour group, if you'll do that thing you said with the boogers I'll make sure they double your soda at snack time.

        • I don't know if I would say androgynous she was skinny and flat chested when she did that movie but she wasn't always.

    • by Anonymous Coward

      You know, a couple of years ago I got real excited because I heard they were making a sequel: Lost City of Z [wikipedia.org]. Even though Brad Pitt quit the film and they replaced him with some dude, I thought it could still be good. But there were no fucking zombies! Every time it started to get good, like when one of the guys is vomiting blood in a scary jungle, or when they run into a bunch of cannibals, the movie would suddenly switch back to England with women in lacy dresses running around and fainting because t

      • Actually the game of "improvise a movie plot for a good laugh" was a fun way to pass time with friends in the 80's. Today, that game would be impossible without offending anyone...
    • by Anonymous Coward

      In the 50s, "Radiation" made superheroes and supervillains. Genetic experiments are our new "radiation".
      In reality, they will probably do as much good and bad as radiation have done. Our expanding knowledge of how genes and biological processes work will do a whole lot of good though.

  • Some DNA is just more equal than others.
  • I guess it's not surprising that millennials never leave home. They can't even find their own shift key.

    After dna, a, t, c, and g, Og somehow managed E. coli (more than once, even, though not in italic).

  • by SuperKendall ( 25149 ) on Friday January 18, 2019 @12:11AM (#57980610)

    A whole bunch of whiners here seem to be worried about this - not one post on super awesome positive human mutations that may occur.

    Live it up a little and stop worrying so much!

    This is just the kind of thing I would think especially the trans-human community would be super into.

    • by AmiMoJo ( 196126 )

      The problem is that we don't have good debugging tools.

      You can test some edits out a bit, maybe try them in other animals, but ultimately you have to run that code in a real human. If it turns out to be buggy it's pretty difficult to patch in-place. Also sometimes it takes ages for the code to crash, like 40 years or more, so the debug/test cycle is pretty slow.

    • Comment removed based on user account deletion
      • The driving force behind direct genetic manipulation is the ability to make non-random changes. Perhaps then the proper word ceases to be evolution, because the process is fast. In any case, choosing the changes wisely means that there need not be much harm to humans from newly designed bad genes.
  • I really hope this is happening in an off-world level 5 containment facility.

  • by Anonymous Coward

    1) Making proteins with unnatural amino acids has been possible and done before.. like a lot of times.
    2) Attaching PEG to proteins, a process called pegylation, has been done before and is a routine process.. although it is rather random. Most pharmaceutically used proteins are pegylated, as the attached PEG seems to make them more long-lived/potent. Making it more specific can be done in much much easier way than this (via Cysteines or surface engineered Lys etc., just to name two options).

    So now they make

  • by Opportunist ( 166417 ) on Friday January 18, 2019 @02:59AM (#57980796)

    OMG,genetically modified bacteria are gonna kill us!

    No. They won't. That's the beauty about this stuff. To be blunt, I'm no big fan of GMO myself, but this is the kind of GMO I could get behind. Why? Because it has a built in kill switch. Those bases X and Y don't exist in the wild. In other words, for your bacteria to live and multiply, you have to keep feeding them these things after artificially creating them. You want your bacteria to die? Just literally starve them to death by not providing X and Y.

    This is the kind of therapeutic GMO bacteria that are just perfect. Use them while you need them, then after they've done their job just cut off their supply of food and they're dying. Beautiful.

    • by djinn6 ( 1868030 )

      I'm sure if you keep them long enough, some of them will eventually evolve the ability to synthesize the new X and Y bases.

      • Standard cell culture techniques help you there, genetic drift is a problem in any cell line so you generally get them behaving well, grow a huge batch and freeze them down, and then only passage lines pulled from storage X times until destroying them. Repeat when stores run out.
        • by djinn6 ( 1868030 )

          That it can be done safely does not mean it will always be done safely. Someone will mess it up given enough time and it only takes one. Now it's hard to quantify what advantages of using the new bases will be evolutionarily speaking, but if there's an advantage, we will eventually see it out in the wild.

      • That was my thought as well. Or to simplify growing this E. coli, we'll genetically engineer a yeast to make X and Y bases. Then that escapes, and all hell breaks loose.

      • by abies ( 607076 )

        I'm sure if you keep them long enough, some of them will eventually evolve the ability to synthesize the new X and Y bases.

        Not necessarily. It might be physically impossible to express bio-machinery required to synthetize X and Y using normal DNA+XY. That would explain why those extra bases never happened in natural world - even if some mutation happened, there was no chance it would be self-sustaining.

  • Are they wholly synthetic or naturally occurring but unused?
    • Protein synthesis works by translating DNA to RNA, then feeding the RNA through a cell structure called a ribosome. Three nucleotide bases code for one amino acid, so the RNA steps through the ribosome three bases at a time (each trio is called a codon), adding one amino acid to the protein chain each time.

      There are more different codons than there are amino acids in nature, but here Life does something clever; the extra codons code for the same or similar amino acids.

      Theoretically it should be possible to

  • Nature is not an idiot. And the 4 billion years of evolution made the base pairs what they are. They should be asking why rather vigorously, not tinkering with the way it is presently. If this gets into human germ cells and is passed along from generation to generation along with other "improvements," may we (humans) not some time in the future be forced to say..."ooops, maybe we shouldn't have done that?"
    • If genes from bacteria from a petri dish get in the human germ line then there's lots of weird questions to ask regardless of if they were GMO or not. Anyhow, look up the amino acid coding sequences and you'll see why they are how they are: contingent chemistry. The third base pair of the triplicate doesn't even matter much of the time. https://upload.wikimedia.org/w... [wikimedia.org]

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