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Cell Metabolism Artificially Enhanced

NewScientist is reporting that Swiss researchers have shown that a cell's metabolism can be increased without altering the genetic makeup. Small plastic packages of enzymes have been successfully inserted into cells, increasing metabolism. "Meier and colleagues coated their polymer vesicles in a chemical that encouraged human white blood cells called macrophages to engulf them. The small capsules contained enzymes, just like natural organelles. The enzymes chosen produced fluorescent chemicals, signaling they were working without problems inside their new host."

2 of 97 comments (clear)

  1. Other Uses by MrMunkey · · Score: 5, Informative

    This is /. so I suppose reading the article isn't a given. There are other uses than just for increasing the metabolism. Other uses include targeting cancerous cells specifically, giving lactose intolerant people enzymes in their stomachs, and making your skin do photosynthesis so you don't even have to eat. They're all theories around the new "NanoReactor" they created for delivering their payloads. I'm assuming that increasing the metabolism was the easiest test to perform in a dish.

  2. What the paper really claims by xplenumx · · Score: 5, Informative
    Tamsin Osborne, who wrote the NewScientistTech article, certainly didn't understand the original article and focused on sensationalism rather than scientific accuracy.

    The original paper did not increase the metabolism of the macrophage. What the original paper did was encage an enzyme, trypsin, in a "nanometer-sized polymer vesicle". This vesicle was coated with a protein that induce macrophages to engulf the vesicle (which is what macrophages do - they phagocytose). The authors then incubated macrophages which contained the vesicles with a dye (BZiPAR) that fluoresces (emits a wavelength of light - in this case green) when treated with trypsin (trypsin cuts of parts of the BZiPAR that suppress fluorescence).

    We already know how to non-genetically introduce proteins to cells, for example using liposomes or the tat-peptide approach. What makes this work interesting is that the polymer vesicle is more stable than liposomes and, unlike the other methods, the vesicles don't release their content into the cell. Instead, the cell's components have to enter into the polymer vesicle.

    This is an interesting technical development. It is not, however, everything that Mr. Osborne makes it out to be.