Recio Maria-Isabel, Gavira José A, de La Torre Jesús, Cano-Muñoz Mario, Martínez-Rodriguez Sergio, Daddaoua Abdelali, Duque Estrella, Ramos Juan L
Estación Experimental del Zaidín, Consejo Superior de Investigaciones Científicas, Granada, Spain.
Consejo Superior de Investigaciones Científicas, Instituto Andaluz de Ciencias de la Tierra, Armilla, Spain.
Protein Sci. 2025 Sep;34(9):e70244. doi: 10.1002/pro.70244.
M2-32 is a non-specific acid phosphatase with a rare ability to function across a broad pH range (3.5-8.5). Analysis using SWISS-PROT Prf Profiles classifies it as a class A acid phosphatase (Z-score: 78.97), sharing 50%-60% sequence similarity with enzymes such as PhoC and PhoN. For detailed characterization, the gene encoding M2-32 was cloned into the pET28(b) vector, overexpressed in Escherichia coli BL21 (DE3), and subsequently purified. Although the monomeric form of M2-32 has a molecular weight of ~28 kDa, size exclusion chromatography, dynamic light scattering, and sedimentation studies revealed a dimeric form in solution. Enzymatic assays using p-nitrophenyl phosphate, 4-methylumbelliferyl phosphate, 3'-and 5'-adenosine monophosphate demonstrated robust activity over a pH range of 4.0-8.0 at both 30 and 50°C. Differential scanning fluorimetry indicated an unfolding temperature close to 47°C; however, the enzyme refolded after heat denaturation at 80°C. We have determined the x-ray crystal structure of M2-32 by molecular replacement using an AlphaFold2-guided truncated model, achieving a resolution of 2.2 Å. The protein crystallized as a dimer-of-dimers. Each monomer (residues 38-274) adopts an all-alpha-helical fold composed of 14 helices and two disulfide bonds. Docking studies with adenosine monophosphates, combined with site-directed mutagenesis, identified His174, Arg207, His213, Asp217 as critical catalytic residues, and Tyr136 and Ser172 probably involved in substrate recognition. Mutations at these positions resulted in over 90% loss of enzymatic activity, highlighting their functional significance.
M2-32是一种非特异性酸性磷酸酶,具有罕见的在较宽pH范围(3.5 - 8.5)发挥作用的能力。使用SWISS-PROT Prf Profiles进行的分析将其归类为A类酸性磷酸酶(Z分数:78.97),与PhoC和PhoN等酶具有50%-60%的序列相似性。为了进行详细表征,将编码M2-32的基因克隆到pET28(b)载体中,在大肠杆菌BL21(DE3)中过表达,随后进行纯化。尽管M2-32的单体形式分子量约为28 kDa,但尺寸排阻色谱、动态光散射和沉降研究表明其在溶液中以二聚体形式存在。使用对硝基苯磷酸酯、4-甲基伞形酮磷酸酯、3'-和5'-腺苷单磷酸进行的酶活性测定表明,在30°C和50°C时,该酶在4.0 - 8.0的pH范围内均具有较强活性。差示扫描荧光法表明其解折叠温度接近47°C;然而,该酶在80°C热变性后可重新折叠。我们通过使用AlphaFold2引导的截短模型进行分子置换,确定了M2-32的X射线晶体结构,分辨率达到2.2 Å。该蛋白质结晶为二聚体的二聚体。每个单体(残基38 - 274)采用由14个螺旋和两个二硫键组成的全α螺旋折叠结构。与腺苷单磷酸的对接研究以及定点诱变相结合,确定His174、Arg207、His213、Asp217为关键催化残基,Tyr136和Ser172可能参与底物识别。这些位置的突变导致酶活性丧失超过90%,突出了它们的功能重要性。