Phosphorylation of Serine 392 Stabilizes the Tetramer Formation of Tumor Suppressor Protein p53

• Published in: Biochemistry (Easton) 1997-08, Vol.36 (33), p.10117-10124
• Main Authors: Sakaguchi, Kazuyasu, Sakamoto, Hiroshi, Lewis, Marc S, Anderson, Carl W, Erickson, John W, Appella, Ettore, Xie, Dong
• Format: Article
• Language: English
• Subjects: Biopolymers; Calorimetry, Differential Scanning; Humans; Phosphorylation; Serine - metabolism; Thermodynamics; Tumor Suppressor Protein p53 - chemistry; Tumor Suppressor Protein p53 - metabolism; Ultracentrifugation
• ISSN: 0006-2960; 1520-4995
• DOI: 10.1021/bi970759w

Tumor suppressor protein p53 is a tetrameric phosphoprotein that activates transcription from several cell cycle regulating genes in response to DNA damage. Tetramer formation is critical to p53's ability to activate transcription; however, posttranslational modifications and protein stabilization also contribute to p53's ability to activate transcription. To determine if phosphorylation affects tetramer formation, we synthesized phosphopeptides corresponding to residues 303−393 of human p53, which includes the domain responsible for tetramer formation. Phosphate was chemically incorporated at Ser315, Ser378, or Ser392 and also at both Ser315 and Ser392. Equilibrium ultracentrifugal analyses showed that phosphorylation at Ser392 increased the association constant for reversible tetramer formation nearly 10-fold. Phosphorylation of either Ser315 or Ser378 had little effect on tetramer formation, but phosphorylation of Ser315 largely reversed the effect of phosphorylation at Ser392. Analyses by calorimetry demonstrated that phosphorylation may influence subunit affinity (and, in turn, DNA binding) by an enthalpy-driven process, possibly between the C-terminal residues and the region immediately adjacent to Ser315. The K d for the tetramer−monomer transition of the unphosphorylated p53 C-terminal domain was determined to be ∼1−10 μM. Thus, in normal, undamaged cells p53 may be largely monomeric. Enhancement of tetramer formation through phosphorylation of Ser392, coupled with a DNA-damage-induced increase in its nuclear concentration, could provide a switch that activates p53 as a transcription factor in response to DNA damage.