Gorelik Alexei, Heinz Leonhard X, Illes Katalin, Superti-Furga Giulio, Nagar Bhushan
From the Department of Biochemistry and Groupe de Recherche Axé sur la Structure des Protéines, McGill University, Montreal, Quebec H3G 0B1, Canada.
the CeMM Research Center for Molecular Medicine, Austrian Academy of Sciences, 1090 Vienna, Austria, and.
J Biol Chem. 2016 Nov 11;291(46):24054-24064. doi: 10.1074/jbc.M116.755801. Epub 2016 Sep 28.
The enzyme acid sphingomyelinase-like phosphodiesterase 3B (SMPDL3B) was shown to act as a negative regulator of innate immune signaling, affecting cellular lipid composition and membrane fluidity. Furthermore, several reports identified this enzyme as an off target of the therapeutic antibody rituximab, with implications in kidney disorders. However, structural information for this protein is lacking. Here we present the high resolution crystal structure of murine SMPDL3B, which reveals a substrate binding site strikingly different from its paralogs. The active site is located in a narrow boot-shaped cavity. We identify a unique loop near the active site that appears to impose size constraints on incoming substrates. A structure in complex with phosphocholine indicates that the protein recognizes this head group via an aromatic box, a typical choline-binding motif. Although a potential substrate for SMPDL3B is sphingomyelin, we identify other possible substrates such as CDP-choline, ATP, and ADP. Functional experiments employing structure-guided mutagenesis in macrophages highlight amino acid residues potentially involved in recognition of endogenous substrates. Our study is an important step toward elucidating the specific function of this poorly characterized enzyme.
酸性鞘磷脂酶样磷酸二酯酶3B(SMPDL3B)被证明是先天性免疫信号的负调节因子,影响细胞脂质组成和膜流动性。此外,一些报告将该酶鉴定为治疗性抗体利妥昔单抗的脱靶,与肾脏疾病有关。然而,该蛋白质的结构信息尚缺。在此,我们展示了小鼠SMPDL3B的高分辨率晶体结构,其揭示了一个与其旁系同源物显著不同的底物结合位点。活性位点位于一个狭窄的靴形腔内。我们在活性位点附近鉴定出一个独特的环,其似乎对进入的底物施加了大小限制。与磷酸胆碱结合的结构表明,该蛋白质通过一个芳香盒(一种典型的胆碱结合基序)识别这个头部基团。尽管SMPDL3B的潜在底物是鞘磷脂,但我们鉴定出了其他可能的底物,如CDP - 胆碱、ATP和ADP。在巨噬细胞中采用结构导向诱变的功能实验突出了可能参与识别内源性底物的氨基酸残基。我们的研究是阐明这种特征不明的酶的特定功能的重要一步。