In vitro validation of Cathepsin S docking models

نویسندگان

چکیده

Abstract In dendritic cells, the dominant lysosomal protease involved in Ii chain degradation and antigen digestion is Cathepsin S, a cysteine papain family. Extracellularly, S also contributes to pathological processes cardiovascular disease, cancer, autoimmune arthritis: unlike most proteases, it retains its activity at serum pH. computational molecular docking studies comparing peptides from literature, we found that shows pH-dependent specificity switch, with predicted dissociation constants for specific peptide sequences differing The aim of this study further characterize switch compare results kinetic parameters vitro. We identified interest docking, including elastin, digested these (LifeTein) using human (Calbiochem), collecting samples LC-MS analysis over 16 hour reaction times. report catalysis both Digestion are compared models predictive catalytic identified. Further investigation needed determine whether selectivity will enable design protein-based therapies inhibitors optimized their targeted microenvironments. This work was partially supported by NIDA/NIH award UG3DA048775, USDA National Institute Food Agriculture, AFRI project #2021-0858, department Biological Systems Engineering Virginia Tech.

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ژورنال

عنوان ژورنال: Journal of Immunology

سال: 2023

ISSN: ['1550-6606', '0022-1767']

DOI: https://doi.org/10.4049/jimmunol.210.supp.221.25