Centre of Molecular Medicine, Institute of Virology, Slovak Academy of Sciences, Dubravska Cesta 9, 845 05 Bratislava, Slovak Republic.
Bioorg Med Chem. 2012 Feb 15;20(4):1403-10. doi: 10.1016/j.bmc.2012.01.007. Epub 2012 Jan 12.
The α-carbonic anhydrase (CA, EC 4.2.1.1) Astrosclerin-3 previously isolated from the living fossil sponge Astrosclera willeyana (Jackson et al., Science 2007, 316, 1893), was cloned, kinetically characterized and investigated for its inhibition properties with sulfonamides and sulfamates. Astrosclerin-3 has a high catalytic activity for the CO(2) hydration reaction to bicarbonate and protons (k(cat) of 9.0×10(5) s(-1) and k(cat)/K(m) of 1.1×10(8) M(-1) × s(-1)), and is inhibited by various aromatic/heterocyclic sulfonamides and sulfamates with inhibition constants in the range of 2.9 nM-8.85 μM. Astrosclerin, and the human isoform CA II, display similar kinetic properties and affinities for sulfonamide inhibitors, despite more than 550 million years of independent evolution. Because Astrosclerin-3 is involved in biocalcification, the inhibitors characterized here may be used to gain insights into such processes in other metazoans.
α-碳酸酐酶(CA,EC 4.2.1.1)Astrosclerin-3 先前从活化石海绵 Astrosclera willeyana(Jackson 等人,Science 2007,316,1893)中分离出来,已被克隆、动力学表征,并研究了其与磺胺类和磺胺酸盐的抑制特性。Astrosclerin-3 对 CO2 水合反应生成碳酸氢盐和质子具有很高的催化活性(kcat 为 9.0×10(5) s(-1),kcat/Km 为 1.1×10(8) M(-1) × s(-1)),并被各种芳香族/杂环磺胺类和磺胺酸盐抑制,抑制常数范围为 2.9 nM-8.85 μM。Astrosclerin 和人同工酶 CA II 尽管经过超过 5.5 亿年的独立进化,但显示出相似的动力学特性和磺胺类抑制剂亲和力。由于 Astrosclerin-3 参与生物钙化,因此这里描述的抑制剂可能用于深入了解其他后生动物的此类过程。