Department of Pharmacology, University of Washington, Seattle, WA 98195, U.S.A.
Department of Biochemistry, Cell and Systems Biology, University of Liverpool, Liverpool L69 7ZB, U.K.
Biochem J. 2023 Jun 28;480(12):875-890. doi: 10.1042/BCJ20230183.
Cushing's syndrome is an endocrine disorder caused by excess production of the stress hormone cortisol. Precision medicine strategies have identified single allele mutations within the PRKACA gene that drive adrenal Cushing's syndrome. These mutations promote perturbations in the catalytic core of protein kinase A (PKAc) that impair autoinhibition by regulatory subunits and compartmentalization via recruitment into AKAP signaling islands. PKAcL205R is found in ∼45% of patients, whereas PKAcE31V, PKAcW196R, and L198insW and C199insV insertion mutants are less prevalent. Mass spectrometry, cellular, and biochemical data indicate that Cushing's PKAc variants fall into two categories: those that interact with the heat-stable protein kinase inhibitor PKI, and those that do not. In vitro activity measurements show that wild-type PKAc and W196R activities are strongly inhibited by PKI (IC50 < 1 nM). In contrast, PKAcL205R activity is not blocked by the inhibitor. Immunofluorescent analyses show that the PKI-binding variants wild-type PKAc, E31V, and W196R are excluded from the nucleus and protected against proteolytic processing. Thermal stability measurements reveal that upon co-incubation with PKI and metal-bound nucleotide, the W196R variant tolerates melting temperatures 10°C higher than PKAcL205. Structural modeling maps PKI-interfering mutations to a ∼20 Å diameter area at the active site of the catalytic domain that interfaces with the pseudosubstrate of PKI. Thus, Cushing's kinases are individually controlled, compartmentalized, and processed through their differential association with PKI.
库欣综合征是一种由应激激素皮质醇过度产生引起的内分泌紊乱。精准医学策略已经确定了 PRKACA 基因内导致肾上腺库欣综合征的单一等位基因突变。这些突变促进了蛋白激酶 A(PKA)催化核心的扰动,通过调节亚基的自动抑制和通过募集到 AKAP 信号岛进行区室化来损害其功能。PKAcL205R 存在于约 45%的患者中,而 PKAcE31V、PKAcW196R、L198insW 和 C199insV 插入突变则不太常见。质谱、细胞和生化数据表明,库欣综合征的 PKAc 变体分为两类:与热稳定蛋白激酶抑制剂 PKI 相互作用的变体,以及不相互作用的变体。体外活性测量显示,野生型 PKAc 和 W196R 活性被 PKI 强烈抑制(IC50<1 nM)。相比之下,PKAcL205R 活性不受抑制剂的阻断。免疫荧光分析表明,PKI 结合的变体野生型 PKAc、E31V 和 W196R 被排除在核外,并免受蛋白水解处理。热稳定性测量显示,在与 PKI 和金属结合核苷酸共孵育时,W196R 变体能够耐受比 PKAcL205 高 10°C 的融解温度。结构建模将 PKI 干扰突变映射到催化结构域活性位点的一个约 20 Å 直径的区域,该区域与 PKI 的伪底物相互作用。因此,库欣综合征激酶通过与 PKI 的差异结合而被单独调控、区室化和加工。