Ben Bdira Fredj, Jiang Jianbing, Kallemeijn Wouter, de Haan Annett, Florea Bogdan I, Bleijlevens Boris, Boot Rolf, Overkleeft Herman S, Aerts Johannes M, Ubbink Marcellus
Department of Macromolecular Biochemistry, Leiden Institute of Chemistry , Einsteinweg 55, 2333 CC Leiden, The Netherlands.
Department of Bio-organic Synthesis, Leiden Institute of Chemistry , Einsteinweg 55, 2333 CC Leiden, The Netherlands.
Biochemistry. 2016 Aug 30;55(34):4823-35. doi: 10.1021/acs.biochem.6b00363. Epub 2016 Aug 16.
Small compound active site interactors receive considerable attention for their ability to positively influence the fold of glycosidases. Endoglycoceramidase II (EGCII) from Rhodococcus sp. is an endo-β-glucosidase releasing the complete glycan from ceramide in glycosphingolipids. Cleavage of the β-glycosidic linkage between glucose and ceramide is also catalyzed by glucocerebrosidase (GBA), the exo-β-glucosidase deficient in Gaucher disease. We demonstrate that established β-glucoside-configured cyclophellitol-type activity-based probes (ABPs) for GBA also are effective, mechanism-based, and irreversible inhibitors of EGCII. The stability of EGCII is markedly enhanced by formation of covalent complexes with cyclophellitol ABPs substituted with hydrophobic moieties, as evidenced by an increased melting temperature, resistance against tryptic digestion, changes in (15)N-(1)H transverse relaxation optimized spectroscopy spectra of the [(15)N]Leu-labeled enzyme, and relative hydrophobicity as determined by 8-anilino-1-naphthalenesulfonic acid fluorescence. The stabilization of EGCII conformation correlates with the shape and hydrophobicity of the substituents of the ABPs. We conclude that the amphipathic active site binders with aliphatic moieties act as a "hydrophobic zipper" on the flexible EGCII protein structure.
小分子活性位点相互作用剂因其对糖苷酶折叠产生积极影响的能力而备受关注。来自红球菌属的内切糖神经酰胺酶II(EGCII)是一种内切β-葡萄糖苷酶,可从糖鞘脂中的神经酰胺释放完整聚糖。葡糖脑苷脂酶(GBA)也催化葡萄糖与神经酰胺之间β-糖苷键的裂解,GBA是戈谢病中缺乏的外切β-葡萄糖苷酶。我们证明,已建立的用于GBA的β-葡萄糖苷构型的环戊糖醇型基于活性的探针(ABP)也是EGCII的有效、基于机制的不可逆抑制剂。用疏水部分取代的环戊糖醇ABP形成共价复合物可显著提高EGCII的稳定性,这通过熔点升高、对胰蛋白酶消化的抗性、[(15)N]亮氨酸标记酶的(15)N-(1)H横向弛豫优化光谱的变化以及由8-苯胺基-1-萘磺酸荧光测定的相对疏水性来证明。EGCII构象的稳定与ABP取代基的形状和疏水性相关。我们得出结论,具有脂肪族部分的两亲性活性位点结合剂在柔性EGCII蛋白质结构上充当“疏水拉链”。