Introduction of C-alkyl branches to l-iminosugars changes their active site binding orientation. Issue 36 (15th July 2022)

• Record Type: Journal Article
• Authors: Kato, Atsushi; Nakagome, Izumi; Yoshimura, Kosuke; Kanekiyo, Uta; Kishida, Mana; Shinzawa, Kenta; Lu, Tian-Tian; Li, Yi-Xian; Nash, Robert J.; Fleet, George W. J.; Tanaka, Nobutada; Yu, Chu-Yi
• Is Part Of: Organic & biomolecular chemistry. Volume 20:Issue 36(2022)
• Page Start: 7250
• Page End: 7260
• Publication Date: 2022-07-15
• Subjects: Chemistry, Organic -- Periodicals; Bioorganic chemistry -- Periodicals; Chemistry, Physical organic -- Periodicals; 547
• DOI: 10.1039/d2ob01099b
• Languages: English
• ISSNs: 1477-0520

Abstract

Abstract : 5- C -Methyl-l - ido -DNJ showed a strong affinity for rhGAA ( K i 0.060 μM). This study provides the first example of a strategy to design high-affinity ligands by introducing alkyl branches into rare sugars and l -sugar-type iminosugars to change the orientation of binding. Abstract : l - ido -Deoxynojirimycin (l - ido -DNJ) itself showed no affinity for human lysosomal acid α-glucosidase (GAA), whereas 5- C -methyl-l - ido -DNJ showed a strong affinity for GAA, comparable to the glucose analog DNJ, with a K i value of 0.060 μM. This excellent affinity for GAA and enzyme stabilization was observed only when methyl and ethyl groups were introduced. Docking simulation analysis revealed that the alkyl chains of 5- C -alkyl-l - ido -DNJs were stored in three different pockets, depending on their length, thereby the molecular orientation was changed. Comparison of the binding poses of DNJ and 5- C -methyl-l - ido -DNJ showed that they formed a common ionic interaction with Asp404, Asp518, and Asp616, but both the binding orientation and the distance between the ligand and each amino acid residue were different. 5- C -Methyl-l - ido -DNJ dose-dependently increased intracellular GAA activity in Pompe patient fibroblasts with the M519V mutation and also promoted enzyme transport to lysosomes. This study provides the first example of a strategy to design high-affinity ligands by introducing alkyl branches into rare sugars and l -sugar-type iminosugars to change the orientation of binding.