Department of Biochemistry, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Proc Natl Acad Sci U S A. 2010 May 11;107(19):8605-10. doi: 10.1073/pnas.0913660107. Epub 2010 Apr 26.
S100A4, a member of the S100 family of Ca(2+)-binding proteins, regulates carcinoma cell motility via interactions with myosin-IIA. Numerous studies indicate that S100A4 is not simply a marker for metastatic disease, but rather has a direct role in metastatic progression. These observations suggest that S100A4 is an excellent target for therapeutic intervention. Using a unique biosensor-based assay, trifluoperazine (TFP) was identified as an inhibitor that disrupts the S100A4/myosin-IIA interaction. To examine the interaction of S100A4 with TFP, we determined the 2.3 A crystal structure of human Ca(2+)-S100A4 bound to TFP. Two TFP molecules bind within the hydrophobic target binding pocket of Ca(2+)-S100A4 with no significant conformational changes observed in the protein upon complex formation. NMR chemical shift perturbations are consistent with the crystal structure and demonstrate that TFP binds to the target binding cleft of S100A4 in solution. Remarkably, TFP binding results in the assembly of five Ca(2+)-S100A4/TFP dimers into a tightly packed pentameric ring. Within each pentamer most of the contacts between S100A4 dimers occurs through the TFP moieties. The Ca(2+)-S100A4/prochlorperazine (PCP) complex exhibits a similar pentameric assembly. Equilibrium sedimentation and cross-linking studies demonstrate the cooperative formation of a similarly sized S100A4/TFP oligomer in solution. Assays examining the ability of TFP to block S100A4-mediated disassembly of myosin-IIA filaments demonstrate that significant inhibition of S100A4 function occurs only at TFP concentrations that promote S100A4 oligomerization. Together these studies support a unique mode of inhibition in which phenothiazines disrupt the S100A4/myosin-IIA interaction by sequestering S100A4 via small molecule-induced oligomerization.
S100A4 是 S100 家族中钙结合蛋白的成员,通过与肌球蛋白 IIA 的相互作用调节癌细胞的迁移。许多研究表明,S100A4 不仅仅是转移性疾病的标志物,而是在转移性进展中具有直接作用。这些观察结果表明,S100A4 是治疗干预的一个极好靶点。使用独特的基于生物传感器的测定法,三氟拉嗪 (TFP) 被鉴定为一种抑制剂,可破坏 S100A4/肌球蛋白 IIA 的相互作用。为了研究 S100A4 与 TFP 的相互作用,我们确定了与人 Ca(2+)-S100A4 结合的 TFP 的 2.3 A 晶体结构。两个 TFP 分子结合在 Ca(2+)-S100A4 的疏水性靶结合口袋内,在复合物形成时未观察到蛋白质的显著构象变化。NMR 化学位移扰动与晶体结构一致,并证明 TFP 在溶液中结合到 S100A4 的靶结合裂隙。值得注意的是,TFP 结合导致五个 Ca(2+)-S100A4/TFP 二聚体组装成紧密堆积的五聚体环。在每个五聚体中,S100A4 二聚体之间的大多数接触都通过 TFP 部分发生。Ca(2+)-S100A4/丙氯拉嗪 (PCP) 复合物表现出类似的五聚体组装。平衡沉降和交联研究表明,在溶液中形成类似大小的 S100A4/TFP 低聚物具有协同性。检测 TFP 阻断 S100A4 介导的肌球蛋白 IIA 丝解聚能力的测定表明,仅在 TFP 浓度促进 S100A4 寡聚化时,才会显著抑制 S100A4 功能。这些研究共同支持一种独特的抑制模式,其中吩噻嗪通过小分子诱导寡聚化将 S100A4 隔离来破坏 S100A4/肌球蛋白 IIA 的相互作用。