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用醉翁藤毒素 III 抑制哺乳动物碳酸酐酶 I-XIV:溶液和计算机模拟研究。

Inhibition of mammalian carbonic anhydrases I-XIV with grayanotoxin III: solution and in silico studies.

机构信息

University of Calgary, Institute for Biocomplexity and Informatics , Calgary, AB , Canada .

出版信息

J Enzyme Inhib Med Chem. 2014 Aug;29(4):469-75. doi: 10.3109/14756366.2013.804072. Epub 2013 Aug 5.

Abstract

Grayanotoxin III (GTX3) was investigated for inhibition of all catalytically active mammalian carbonic anhydrase (CA, EC 4.2.1.1) isoforms, i.e. CA I to CA XIV. It showed micromolar inhibition (KIs of 8.01 and 6.13 µM) for cytosolic isoforms CA I and II, respectively. GTX3 showed a submicromolar inhibition (KIs in the range of 0.51-2.15 µM) for the remaining cytosolic (CA III, VII and XIII), membrane-associated/transmembrane (CA IV, IX, XII and XIV), mitochondrial (CA VA and CA VB) and secreted (CA VI) isoforms. This inhibition profile is very different from that of the sulfonamide CA inhibitors (CAIs), which possess different clinical applications. A molecular docking study for GTX3 within the active sites of CA I and II assisted to the understanding of molecular mechanism of the ligand. The interesting inhibition profile, coupled with various possibilities of interacting with the enzyme active site make this family of natural compounds attractive leads for designing novel chemotypes acting as CAIs.

摘要

格雷西毒素 III(GTX3)被研究用于抑制所有具有催化活性的哺乳动物碳酸酐酶(CA,EC 4.2.1.1)同工酶,即 CA I 至 CA XIV。它对细胞质同工酶 CA I 和 CA II 的抑制作用分别为微摩尔级(KIs 为 8.01 和 6.13 µM)。GTX3 对其余的细胞质(CA III、VII 和 XIII)、膜相关/跨膜(CA IV、IX、XII 和 XIV)、线粒体(CA VA 和 CA VB)和分泌(CA VI)同工酶的抑制作用为亚微摩尔级(KIs 范围为 0.51-2.15 µM)。这种抑制谱与磺酰胺 CA 抑制剂(CAIs)非常不同,后者具有不同的临床应用。GTX3 在 CA I 和 II 的活性部位进行的分子对接研究有助于理解配体的分子机制。有趣的抑制谱,加上与酶活性位点相互作用的各种可能性,使这一系列天然化合物成为设计新型作为 CAIs 作用的化学型的有吸引力的先导化合物。

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