Protein Profiling of Active Cysteine Cathepsins in Living Cells Using an Activity-Based Probe Containing a Cell-Penetrating Peptide

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• 作者：Fengkai Fan ; Si Nie ; Eric B. Dammer ; Duc M. Duong ; Deng Pan ; Lingyan Ping ; Linhui Zhai ; Junzhu Wu ; Xuechuan Hong ; Lingsong Qin ; Ping Xu ; Yu-Hui Zhang
• 刊名：Journal of Proteome Research
• 出版年：2012
• 出版时间：December 7, 2012
• 年：2012
• 卷：11
• 期：12
• 页码：5763-5772
• 全文大小：387K
• 年卷期：v.11,no.12(December 7, 2012)
• ISSN：1535-3907

文摘

Cell-permeable activity-based probes (ABPs) are capable of labeling target proteins in living cells, thereby providing a powerful tool for profiling active enzymes in their native environment. In this study, we describe the synthesis and use of a novel trifunctional cell-permeable activity-based probe (TCpABP) for proteomic profiling of active cysteine cathepsins in living cells. We demonstrate that although TCpABP contains cell-impermeable tags, it was able to enter living cells efficiently via the delivery of a cell-penetrating peptide. TCpABP also allowed simultaneous detection and affinity isolation of labeled proteins with a fluorophore and a biotin motif, respectively. We optimized the enrichment protocol to minimize contaminants and identified 7 cathepsins, 2 of which have never been identified using existing ABPs. We also used a label-free quantification approach to quantify the relative abundances of active cathepsins and compared them with their previously published mRNA expression levels. A high degree of correlation between the mRNA expression levels and protein relative activities was observed for most of the identified cathepsins except cathepsin H. The results herein indicate that TCpABP is valuable for the detection of active cathepsins in living cells and provides useful guidelines for designing novel cell-permeable ABPs for in vivo labeling and their applications in in vivo proteomics studies.

Keywords:

activity-based probe; cell-penetrating peptide; cathepsin; proteomics; living cell