Proteasome inhibitors: an expanding army attacking a unique target - PubMed (original) (raw)
Review
Proteasome inhibitors: an expanding army attacking a unique target
Alexei F Kisselev et al. Chem Biol. 2012.
Abstract
Proteasomes are large, multisubunit proteolytic complexes presenting multiple targets for therapeutic intervention. The 26S proteasome consists of a 20S proteolytic core and one or two 19S regulatory particles. The 20S core contains three types of active sites. Many structurally diverse inhibitors of these active sites, both natural product and synthetic, have been discovered in the last two decades. One, bortezomib, is used clinically for treatment of multiple myeloma, mantle cell lymphoma, and acute allograft rejection. Five more recently developed proteasome inhibitors are in trials for treatment of myeloma and other cancers. Proteasome inhibitors also have activity in animal models of autoimmune and inflammatory diseases, reperfusion injury, promote bone and hair growth, and can potentially be used as anti-infectives. In addition, inhibitors of ATPases and deubiquitinases of 19S regulatory particles have been discovered in the last decade.
Copyright © 2012 Elsevier Ltd. All rights reserved.
Figures
Figure 1. The Proteasome
(A) The 26S particle. Location and functions of different subunits are indicated. (B) Cross-section of the 20S proteolytic core showing location of the active sites. (C) The catalytic mechanism of the proteasome. Proteasome is blue. Substrate is black except for scissile bond, which is red.
Figure 2. Representatives of the Major Classes of Covalent Proteasome Inhibitors
(A) Aldehydes; (B) boronates; (C) epoxyketones; (D) α-ketoaldehyde; (E) β-lactones; (F) vinyl-sulfones; (G) syrbactines; (H) bacteria-specific oxatiazol-2-ones. Natural products are blue. Synthetic inhibitors used clinically for the treatment of cancer (FDA-approved or in clinical trials) are red; natural product in clinical trials for the treatment of cancer is purple. Synthetic inhibitors that were tested clinically for other indications are orange. (Omuralide is a derivative of a natural product lactacystin.)
Figure 3. Mechanism of Proteasome Inhibition by Covalent Inhibitors
(A) Aldehydes; (B) boronates; (C) epoxyketones; (D) α-ketoaldehyde; (E) β-lactones; (F) vinyl-sulfones; (G) syrbactines; (H) bacteria-specific oxatiazol-2-ones. Proteasome is blue. Inhibitors are black except for electrophiles, which are red.
Figure 4. Noncovalent Proteasome Inhibitors
(A) Cyclic peptides. (B) N- and C-terminally capped dipeptides. (C) Others.
Figure 5. Site-Specific Inhibitors
(A) Inhibitors of the chymotrypsin-like sites: YU-101 (Elofsson et al., 1999), NC-005 (Britton et al., 2009), NC-005-VS (Screen et al., 2010), and LU-005 (Geurink et al., 2010). (B) Inhibitors of the caspase-like sites. YU-102 (Myung et al., 2001), NC-001 (Britton et al., 2009), and LU-001 (van der Linden et al., 2012) inhibit β1 and β1i sites. (C) Inhibitor of the trypsin-like sites (Mirabella et al., 2011). (D) Inhibitors with selectivity for immunoproteasome subunits over their constitutive counterparts and vice versa. PR-957 (Muchamuel et al., 2009) is β5i (LMP7)-selective, and CPSI (Parlati et al., 2009) is β5-selective. LMP2-sp-ek (Ho et al., 2007) and IPSI-001 (Kuhn et al., 2009) are β1i (LMP2)-selective. (E) Activity-based probes (Mirabella et al., 2011; Verdoes et al., 2010). Azido-NC-002 requires subsequent modification by a biotinylated phospane in a Staudinger-Bertozzi ligation to reveal polypeptides modified by the probe.
Figure 6
Inhibitors of 19S RP
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