B. Sandler et al., SPECIFICITY OF POLYCLONAL ANTI-P53 IGG FOR ISOLATION OF THE SOLUBLE P53 ANTIGEN FROM HUMAN SERUM, INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 1(4), 1998, pp. 767-770
The possibility to use anti-p53 IgG for isolation of the soluble p53 a
ntigen as a serological tumor marker has been shown in our previous st
udies. In order to prove the specificity of such IgG, we compared the
effectiveness of columns with anti-p53 IgG and IgG isolated from non-t
reated rabbits (regular IgG). The gel fiberglass (GFG) columns for aff
inity chromatography were prepared separately with both types of IgG.
The same serum was percolated simultaneously through both columns and
the results of elution were compared. The total concentration of tumor
-associated antigens (TAA) eluted from the serum of cancer patients wa
s similar in both TAA mixtures isolated either with anti-p53 IgG or wi
th the regular IgG. Differences are manifest in the content of total p
roteins and amount of each eluted protein: a mixture eluted with the r
egular IgG contains several proteins whereas the anti-p53 IgG isolated
only two proteins, p64 and p53. The amount of the soluble p53 antigen
isolated from the cancer serum was significantly higher when it was i
solated with anti-p53 IgG. The method developed in our laboratory was
shown to be highly specific both to isolate proteins related to cancer
(p53) and non-cancer disorders (p64). Data presented in this report s
how that such specificity can be achieved only if the anti-p53 IgG is
used: the regular IgG obtained from non-treated animals isolate many p
roteins among which the concentration of specific p53 protein is lost.