Comparative analysis of p21 proteins from various cell types by two‐dimensional gel electrophoresis

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Abstract
The products of the ras gene family arc related proteins at a molecular weight of 21 kDa, designated p21. In the present study we used two‐dimensional gel electrophoresis to compare p21 proteins from five different normal and malignant cell lines. Using a known protein (3H‐labeled translation initiation factor [elF‐4D]) as a standard internal marker for isoelectric point (pI), we show that p2l proteins from various cells differ only slightly in molecular weight (21–24 kDa) but express a wide variety in charge (pl 4.8 to 7) that could only be detected by the use of two‐dimensional gel electrophoresis. p21 in NIH/3T3 cells was expressed as a single protein, which migrated at 21 kDa and pl 5.1. This peptide, which is probably the product of the normal cellular ras gene, was also detected in normal human lymphocytes. The synthesis of this peptide was not elevated in the transformed cells. However, transformation of NIH/3T3 fibroblasts and of human leukocytes was found to be associated with expression of qualitatively different forms of p21 peptides. Four additional p21‐associated peptides of identical molecular weight (23 kDa), but multiple charge forms, were detected selectively in Kirsten murine sarcoma virus‐transformed NIH/3T3 cells. Transformation of cells with Harvey murine sarcoma virus was found to be associated with prominent expression of two major pairs of p21‐associated proteins, one at 21 kDa (pl, 5.2 and 5.3) and the other at 23 kDa (pl, 5.1 and 5.2). In HL‐60 leukemic cells there was an additional, more acidic form (pl 5.0) of p21, which appeared to be absent or reduced in normal human lymphocytes. These results indicate that p21 from viral origin or cellular origin might be expressed in the cells in multiple charge forms. The capability to distinguish multiple forms of p21 and slight charge modifications associated with malignancy should call for the use of 2‐D gel electrophoresis as an important tool in future studies involving p21 proteins.