Tuesday, January 23, 2007

References

References



  • Ref_ER_LUMEN: DePierre, J.W.; Dallner, G. Structural Aspects of the membrane of the Endoplasmic reticulum. Biochim. Biophys. Act. 415:411-472,1975
  • Jennifer J. Smith1, Marcello Marelli1, Rowan H. Christmas1, Franco J. Vizeacoumar2, David J. Dilworth1, Trey Ideker1, Timothy Galitski1, Krassen Dimitrov1, Richard A. Rachubinski2 and John D. Aitchison. Transcriptome profiling to identify genes involved in peroxisome assembly and function. The Journal of Cell Biology, Volume 158, Number 2, July 22, 2002 259-271
  • Li X, Baumgart E, Dong GX, Morrell JC, Jimenez-Sanchez G, Valle D, Smith KD, Gould SJ. PEX11alpha is required for peroxisome proliferation in response to 4-phenylbutyrate but is dispensable for peroxisome proliferator-activated receptor alpha-mediated peroxisome proliferation. Mol Cell Biol. 2002 Dec;22(23):8226-40.
  • Sacksteder KA, Jones JM, South ST, Li X, Liu Y, Gould SJ. PEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesis. J Cell Biol. 2000 Mar 6;148(5):931-44.


    Please send questions/comments/suggestions to: Mark Dalton at markwdalton@gmail.com

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  • Tuesday, January 10, 2006

    Chapter 2.2.7: Peroxisomes


    Peroxisomes


    It used to be thought that peroxisomes are formed by the budding of
    smooth Endoplasmic Reticulum (ER). However, now it is thought that they
    form through self-assembly.
    (reference)
    The peroxisome is another major source of Oxygen utilization (along with
    the mitochondrion). There are specific proteins associated with the
    peroxisomes membrane, also there are 3 oxidation enzymes associated with
    peroxisomes:

  • D-amino acid oxidase
  • Urate Oxidase
  • Catalase

  • The enzyme contents vary with various types of cells. One of the main
    functions of peroxisomes in liver cells is detoxification. This is
    done by the oxidation of substances like:

  • Alcohol - About 1/2 of the ethanol one drinks is converted to
    acetaldehyde by oxidation.
  • Phenols
  • Formic acid
  • Formaldehyde

  • Why peroxisomes are not like lysosomes.

    Peroxisomes are organelles that contain oxidative enzymes, such as D-amino acid
    oxidase, urate oxidase, and catalase. They may resemble a lysosome, however,
    they are not formed in the Golgi complex. Peroxisomes are distinguished by a
    crystalline structure inside a sac which also contains amorphous gray material.
    They are self replicating, like the mitochondria. Components accumulate at a
    given site and they can be assembled into a peroxisome. They may look like
    storage granules, however, they are not formed in the same way as storage
    granules.


    Peroxisomes function to rid the body of toxic substances like hydrogen
    peroxide, or other metabolites. They are a major site of oxygen utilization
    and are numerous in the liver where toxic byproducts are going to accumulate.

    The peroxisome is made as a phospholipid bilayer, encapsulating oxidative
    materials. They would be 'sphere-ish' in shape, not necessarily a
    perfect sphere, and sometimes, they may take other shapes. But most
    electron micrographs I have seen (2 dimensions) show them as circles.
    (As you may be aware, the Cell membrane is also a phospholipid bilayer.)
    Peroxisomes have membrane proteins that are critical for peroxisomal function,
    to import proteins into their interiors, proliferate or segregate to daughter cells
    (reference)
    The main differences would be:

    1. Types of phospholipids used.
    2. Size of the membrane (i.e. peroxisomes are MUCH smaller
    than the cell).



    Please send questions/comments/suggestions to: Mark Dalton at markwdalton@gmail.com.

    Chapter 2.1.5: Na _ K ATPase (Sodium-Potassium ATPase pump)



    This is both an example of how Active anti-port and co-transport works
    and an example showing part of how nerves and other cells generate a
    electrical potential on their membrane surfaces.



    Please send questions/comments/suggestions to: Mark Dalton at markwdalton@gmail.com.