Details

Autor(en) / Beteiligte

• Gillet, Ludovic C.J.
• Namoto, Kenji
• Ruchti, Alexandra
• Hoving, Sjouke
• Boesch, Danielle
• Inverardi, Bruno
• Mueller, Dieter
• Coulot, Michele
• Schindler, Patrick
• Schweigler, Patrick
• Bernardi, Anna
• Gil-Parrado, Shirley

Titel

In-cell Selectivity Profiling of Serine Protease Inhibitors by Activity-based Proteomics

Ist Teil von

• Molecular & cellular proteomics, 2008-07, Vol.7 (7), p.1241-1253

Ort / Verlag

United States: Elsevier Inc

Erscheinungsjahr

2008

Quelle

Free E-Journal (出版社公開部分のみ）

Beschreibungen/Notizen

• Activity-based proteomics is a methodology that is used to quantify the catalytically active subfraction of enzymes present in complex mixtures such as lysates or living cells. To apply this approach for in-cell selectivity profiling of inhibitors of serine proteases, we designed a novel activity-based probe (ABP). This ABP consists of (i) a fluorophosphonate-reactive group, directing the probe toward serine hydrolases or proteases and (ii) an alkyne functionality that can be specifically detected at a later stage with an azide-functionalized reporter group through a Cu(I)-catalyzed coupling reaction (“click chemistry”). This novel ABP was shown to label the active site of several serine proteases with greater efficiency than a previously reported fluorophosphonate probe. More importantly, our probe was cell-permeable and achieved labeling of enzymes within living cells with efficiency similar to that observed for the corresponding lysate fraction. Several endogenous serine hydrolases whose activities were detected upon in-cell labeling were identified by two-dimensional gel and MS analyses. As a proof of principle, cell-permeable inhibitors of an endogenous serine protease (prolyl endopeptidase) were assessed for their potency and specificity in competing for the in situ labeling of the selected enzyme. Altogether these results open new perspectives for safety profiling studies in uncovering potential cellular “side effects” of drugs (unanticipated off-target inhibition or activation) that may be overlooked by standard selectivity profiling methods.