Human Saposin B Ligand Binding and Presentation to alpha-Galactosidase A.
Sawyer, T.K., Aral, E., Staros, J.V., Bobst, C.E., Garman, S.C.(2024) bioRxiv 
- PubMed: 38617236 
- DOI: https://doi.org/10.1101/2024.04.04.584535
- Primary Citation of Related Structures:  
9AVS, 9AXG - PubMed Abstract: 
Sphingolipid activator protein B (saposin B; SapB) is an essential activator of globotriaosylceramide (Gb3) catabolism by ¦Á-galactosidase A. However, the manner by which SapB stimulates ¦Á-galactosidase A activity remains unknown. To uncover the molecular mechanism of SapB presenting Gb3 to ¦Á-galactosidase A, we subjected the fluorescent substrate globotriaosylceramide-nitrobenzoxidazole (Gb3-NBD) to a series of biochemical and structural assays involving SapB. First, we showed that SapB stably binds Gb3-NBD using a fluorescence equilibrium binding assay, isolates Gb3-NBD from micelles, and facilitates ¦Á-galactosidase A cleavage of Gb3-NBD in vitro . Second, we crystallized SapB in the presence of Gb3-NBD and validated the ligand-bound assembly. Third, we captured transient interactions between SapB and ¦Á-galactosidase A by chemical cross-linking. Finally, we determined the crystal structure of SapB bound to ¦Á-galactosidase A. These findings establish general principles for molecular recognition in saposin:hydrolase complexes and highlight the utility of NBD reporter lipids in saposin biochemistry and structural biology.
Organizational Affiliation: 
Department of Biochemistry & Molecular Biology, Institute of Applied Life Sciences, University of Massachusetts, Amherst, Massachusetts 01003, USA.