Immunological detection of ecto-ATPase in chicken and rat tissues: characterization, distribution, and a cautionary note

• Published in: Biochemistry and molecular biology international Vol. 45; no. 5; p. 1057
• Main Authors: Smith, T M, Carl, S A, Kirley, T L
• Format: Journal Article
• Language: English
• Published: England 01.08.1998
• Subjects: Adenosine Triphosphatases - analysis; Adenosine Triphosphatases - chemistry; Adenosine Triphosphatases - immunology; Animals; Antibody Specificity; Blotting, Western; Cell Membrane - enzymology; Chickens; Cross Reactions; Fluorescent Antibody Technique, Indirect; Gizzard, Avian - enzymology; Immune Sera; Muscle, Smooth - enzymology; Organ Specificity; Precipitin Tests; Rats; Stomach - enzymology
• ISSN: 1039-9712
• DOI: 10.1002/iub.7510450523

We have generated a polyclonal antibody (CKG2) against native chicken gizzard ecto-ATPase for immunolocalization and immunoprecipitation. Active ecto-ATPase is immunoprecipitated from solubilized chicken and rat membranes and shown to be localized to the plasma membrane of the chicken smooth muscle cells. This antibody is specific for the ecto-ATPases, since the more abundant chicken stomach ecto-apyrase is not recognized in immunoprecipitation, western blot or immunolocalization analyses. The CKG2 antibody cross-reacts with mammalian (rat) ecto-ATPase in western blots, with testis being the most abundant source. Interestingly, when the same rat membranes are analyzed by western blot under non-reducing conditions, the 66 kDa ecto-ATPase is not recognized, instead a 200 kDa protein is detected, previously postulated to be an oligomer of ecto-ATPase. However, this 200 kDa cross-reacting protein is not related to the ecto-ATPases, but is instead an immunoglobulin binding protein, comprised of 50 kDa subunits.