Abstract
Isolation of acidic proteins with high affinity for DNA and/or nucleohistone, from rat liver chromatin, is described. It is rapid and avoids the use of harsh extraction conditions. The isolated proteins comprise less than 4% of the total nuclear proteins, and are distinct from the other major groups of nuclear proteins in their solubility properties and SDS-acrylamide gel electrophoresis patterns. They bind to DNA 5 to 7 times more effectively than other nuclear acidic proteins.
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