Apoptin Induces Tumor-specific Apoptosis as a Globular Multimer

• Published in: The Journal of biological chemistry Vol. 278; no. 11; pp. 9042 - 9051
• Main Authors: Leliveld, Sirik R, Zhang, Ying-Hui, Rohn, Jennifer L, Noteborn, Mathieu H M, Abrahams, Jan Pieter
• Format: Journal Article
• Language: English
• Published: United States American Society for Biochemistry and Molecular Biology 14-03-2003
• Subjects: Amino Acid Motifs; Apoptosis; Blotting, Western; Calibration; Capsid - metabolism; Capsid - physiology; Capsid Proteins; Carrier Proteins - metabolism; Chicken anemia virus - metabolism; Chromatography; Circular Dichroism; Cloning, Molecular; Cross-Linking Reagents - pharmacology; Detergents - pharmacology; Dimerization; Electrophoresis, Polyacrylamide Gel; Escherichia coli - metabolism; Genetic Vectors; Light; Maltose-Binding Proteins; Microscopy, Atomic Force; Microscopy, Electron; Microscopy, Fluorescence; Open Reading Frames; Protein Binding; Protein Conformation; Protein Folding; Protein Structure, Quaternary; Protein Structure, Secondary; Protein Structure, Tertiary; Recombinant Fusion Proteins - metabolism; Recombinant Proteins - chemistry; Recombinant Proteins - metabolism; Scattering, Radiation; Spectrometry, Fluorescence; Transfection; Zinc - metabolism
• DOI: 10.1074/jbc.M210803200
• EISSN: 1083-351X
• ISSN: 0021-9258

The chicken anemia virus-derived Apoptin protein induces tumor-specific apoptosis. Here, we show that recombinant Apoptin
protein spontaneously forms non-covalent globular aggregates comprising 30 to 40 subunits in vitro . This multimerization is robust and virtually irreversible, and the globular aggregates are also stable in cell extracts,
suggesting that they remain intact within the cell. Furthermore, studies of Apoptin expressed in living cells confirm that
Apoptin indeed exists in large complexes in vivo . We map the structural motifs responsible for multimerization in vitro and aggregation in vivo to the N-terminal half of the protein. Moreover, we show that covalently fixing the Apoptin monomers within the recombinant
protein multimer by internal cross-linking does not affect the biological activity of Apoptin, as these fixed aggregates exhibit
similar tumor-specific localization and apoptosis-inducing properties as non-cross-linked Apoptin. Taken together, our results
imply that recombinant Apoptin protein is a multimer when inducing apoptosis, and we propose that this multimeric state is
an essential feature of its ability to do so. Finally, we determine that Apoptin adopts little, if any, regular secondary
structure within the aggregates. This surprising result would classify Apoptin as the first protein for which, rather than
the formation of a well defined tertiary and quaternary structure, semi-random aggregation is sufficient for activity.