Interaction of sodium dodecyl sulfate and of non-ionic detergents with S-carboxyamidomethyl-k-casein.

Sodium dodecyl sulfate binds to S-carboxyamidomethyl-k-casein in a highly cooperative manner at a concentration near the critical micelle concentration, showing a strong dependence on ionic strength. The maximum number of sodium dodecyl sulfate molecules bound is attained above the critical micelle concentration, and is very close to the micelle aggregation number in the absence of protein. The binding sites on the protein for sodium dodecyl sulfate are localized mainly on para-k-casein part, which is a hydrophobic fragment of k-casein produced by rennin attack. The mode of the action of sodium dodecyl sulfate on S-carboxyamidomethyl-k-casein resembles that of several integral membrane proteins, rather than of water soluble proteins. On considering possible situations, it is suggested that the unusual interaction of S-carboxyamidomethyl-k-casein with sodium dodecyl sulfate is responsible for an anomalous migration of reduced k-casein observed in sodium dodecyl sulfate polyacrylamide gel electrophoresis. Further, the suggestion was made by the binding studies of sodium dodecyl sulfate and non-ionic detergents that the sites which were involved in self-association of S-carboxyamidomethyl-k-casein participated in the binding sites of detergents.