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Design of cell-permeable, fluorescent activity-based probes for the lysosomal cysteine protease asparaginyl endopeptidase (AEP)/legumain
- Source :
-
Bioorganic & Medicinal Chemistry Letters . Feb2007, Vol. 17 Issue 3, p649-653. 5p. - Publication Year :
- 2007
-
Abstract
- Abstract: Asparaginyl endopeptidase (AEP), also known as legumain, is a cysteine protease that has been ascribed roles in antigen presentation yet its exact role in human biology remains poorly understood. We report here, the use of a positional scanning combinatorial library of peptide AOMKs containing a P1 aspartic acid to probe the P2, P3, and P4 subsite specificity of endogenous legumain. Using inhibitor specificity profiles of cathepsin B and legumain, we designed fluorescent ABPs that are highly selective, cell-permeable reagents for monitoring legumain activity in complex proteomes. [Copyright &y& Elsevier]
- Subjects :
- *ELECTRONIC probes
*ENDOPEPTIDASES
*PROTEOLYTIC enzymes
*LYSOSOMES
Subjects
Details
- Language :
- English
- ISSN :
- 0960894X
- Volume :
- 17
- Issue :
- 3
- Database :
- Academic Search Index
- Journal :
- Bioorganic & Medicinal Chemistry Letters
- Publication Type :
- Academic Journal
- Accession number :
- 23740346
- Full Text :
- https://doi.org/10.1016/j.bmcl.2006.10.100