AMPK Methods and Protocols

(Rick Simeone) #1

  1. Protein concentration is measured in supernatants by Lowry
    method using BIO-RAD protein assay kit in a 96-well plate.

  2. 20μg of total protein is diluted with H 2 Oto20μl total
    volume, mixed with 5μlof4loading buffer and heated at
    100 C for 3 min. Samples are ready for loading on SDS PAGE
    (seeNote 22).


SDS polyacrylamide gel electrophoresis



  1. For a 10% SDS PAGE, mix 2.65 ml of H 2 O, 3.35 ml of
    acrylamide/bisacrylamide solution, 500μl of SDS (5%), and
    3.75 ml of Tris-HCl (1 M, pH 8.8). Polymerization is started
    by addition of 75μl of 10% (w/v) APS and 15μl of TEMED.

  2. For the 3.6% stacking gel, mix 1.75 ml of H 2 O, 0.5 ml of
    acrylamide/bisacrylamide solution, 100μl of 5% SDS, and
    2.5 ml of Tris–HCl (0.25 M, pH 6.8). Polymerization is started
    by addition of 75μl of 10% (w/v) APS and 10μl of TEMED.

  3. The samples are loaded and separated electrophoretically at
    150 V until the protein reach the running gel and then at
    200 V for about 1 h until the bromophenol dye front run off
    the gel.


Immunoblotting



  1. After electrophoresis, separate the gel plates and remove the
    stacking gel.

  2. The PVDF membrane is immerged in ethanol and then in H 2 O
    to make it hydrophilic.

  3. The 10% gel can be then blotted according to the wet blotting
    method.

  4. First, two sponges, six Whatman filter papers, and the PVDF
    membrane are equilibrated in blotting transfer buffer for
    30 min.

  5. The holder cassette is set inside the container containing blot-
    ting transfer buffer with the black side facing down.

  6. Then the apparatus is prepared as followed from the cathode:
    one sponge, three filter papers, the gel, the PVDF membrane,
    three filter papers, and one sponge.

  7. Bubbles are removed by rolling over filter paper using a 15 ml
    tube. The holder cassette is then closed and placed in the
    container (seeNote 23).

  8. The container is placed into the blotting chamber. Place a
    cooling unit into the chamber, fill with blotting transfer buffer.

  9. The blotting is performed for 1 h at 100 V.
    Antibodies

  10. After the transfer, incubate the PVDF membrane with block-
    ing solution for 1 h at room temperature on a stirring plate.


Study of Cardiac Hypertrophy and Protein Synthesis 333
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