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      A role for a 70-kilodalton heat shock protein in lysosomal degradation of intracellular proteins.

      Science (New York, N.Y.)
      Amino Acid Sequence, Animals, Cells, Cultured, Heat-Shock Proteins, genetics, physiology, Immunoblotting, Lysosomes, metabolism, Molecular Sequence Data, Rats, Ribonuclease, Pancreatic, Sequence Homology, Nucleic Acid

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          Abstract

          A 73-kilodalton (kD) intracellular protein was found to bind to peptide regions that target intracellular proteins for lysosomal degradation in response to serum withdrawal. This protein cross-reacted with a monoclonal antibody raised to a member of the 70-kD heat shock protein (hsp70) family, and sequences of two internal peptides of the 73-kD protein confirm that it is a member of this family. In response to serum withdrawal, the intracellular concentration of the 73-kD protein increased severalfold. In the presence of adenosine 5'-triphosphate (ATP) and MgCl2, the 73-kD protein enhanced protein degradation in two different cell-free assays for lysosomal proteolysis.

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