Differential Detergent Fractionation of Eukaryotic Cells
Adapted from Proteins and Proteomics (ed. Simpson). CSHL Press, Cold Spring Harbor, NY, USA, 2003.INTRODUCTION
Differential detergent fractionation (DDF) involves the sequential extraction of cells with PIPES buffers containing first digitonin, then Triton, and finally Tween/deoxycholate (DOC). The procedure yields four biochemically and electrophoretically distinct fractions composed of the following: (1) cytosolic proteins and extractable cytoskeletal elements; (2) membrane and organelle proteins; (3) nuclear membrane proteins and extractable nuclear proteins; (4) detergent-resistant cytoskeletal filaments and nuclear matrix proteins. Most of these fractions can be enriched or purified further by subsequent manipulations. The DDF protocol described here represents a modification of a method used for the fractionation of Madin-Darby canine kidney cells, including the addition of a digitonin extraction step, the inclusion of EDTA in the digitonin and Triton buffers, and the elimination of a nuclease digestion step; DNA is instead denatured by shear force in the presence of sodium dodecyl sulfate (SDS).
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