Identifying selective inhibitors against the human cytosolic sialidase NEU2 by substrate specificity studies

Yanhong Li, Hongzhi Cao, Hai Yu, Yi Chen, Kam Lau, Jingyao Qu, Vireak Thon, Go Sugiarto, Xi Chen

Research output: Contribution to journalArticlepeer-review

41 Scopus citations


Aberrant expression of human sialidases has been shown to associate with various pathological conditions. Despite the effort in the sialidase inhibitor design, less attention has been paid to designing specific inhibitors against human sialidases and characterizing the substrate specificity of different sialidases regarding diverse terminal sialic acid forms and sialyl linkages. This is mainly due to the lack of sialoside probes and efficient screening methods, as well as limited access to human sialidases. A low cellular expression level of the human sialidase NEU2 hampers its functional and inhibitory studies. Here we report the successful cloning and expression of the human sialidase NEU2 in E. coli. About 11 mg of soluble active NEU2 was routinely obtained from 1 L of E. coli cell culture. Substrate specificity studies of the recombinant human NEU2 using twenty p-nitrophenol (pNP)-tagged α2-3- or α2-6-linked sialyl galactosides containing different terminal sialic acid forms including common N-acetylneuraminic acid (Neu5Ac), non-human N-glycolylneuraminic acid (Neu5Gc), 2-keto-3-deoxy-d-glycero-d- galacto-nonulosonic acid (Kdn), or their C5-derivatives in a microtiter plate-based high-throughput colorimetric assay identified a unique structural feature specifically recognized by the human NEU2 but not two bacterial sialidases. The results obtained from substrate specificity studies were used to guide the design of a sialidase inhibitor that was selective against human NEU2. The selectivity of the inhibitor was revealed by the comparison of sialidase crystal structures and inhibitor docking studies.

Original languageEnglish (US)
Pages (from-to)1060-1072
Number of pages13
JournalMolecular BioSystems
Issue number4
StatePublished - Apr 1 2011

ASJC Scopus subject areas

  • Biotechnology
  • Molecular Biology


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