Abstract
Aims: This study aims to identify the potential of papain as a candidate for the treatment modality for abnormal scars via in silico studies. Methods: We determined the potential mechanism of the process of collagen degradation by papain by investigating its cleavage site-specificity and identifying human papain-like enzymes that have comparable biological activity in degrading collagen in the extracellular matrix using Merops, Bioedit, String DB and Cytoscape software. Results: Papain targets QQ_D (Glutamine-Glutamine Aspartic acid) motif for degradation while collagen only has QQ (Glutamine-Glutamine) motif. Additionally, the homology result showed that Cathepsin B has a closer relationship with papain compared with another candidate, Cathepsin K. Conclusion: Papain is a potential therapeutical modality candidate in degrading collagen in abnormal scars with an indirect mechanism as indicated by its cleavage site-specificity and its relationship with Cathepsin B, which degrades collagen via ubiquitin (UBC) proteasome.
| Original language | English |
|---|---|
| Pages (from-to) | 4957-4962 |
| Number of pages | 6 |
| Journal | Research Journal of Pharmacy and Technology |
| Volume | 14 |
| Issue number | 9 |
| DOIs | |
| Publication status | Published - Sept 2021 |
Keywords
- Abnormal scar
- Cathepsin
- In silico
- Papain enzyme
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