The rise of covalent proteolysis targeting chimeras

被引:49
作者
Gabizon, Ronen [1 ]
London, Nir [1 ]
机构
[1] Weizmann Inst Sci, Dept Organ Chem, IL-7610001 Rehovot, Israel
基金
以色列科学基金会;
关键词
Covalent PROTACs; Targeted degradation; Chemoproteomics; E3; li-; gases; Reversible covalent; SMALL-MOLECULE; PROTEIN-DEGRADATION; UBIQUITIN LIGASE; STRUCTURAL BASIS; INHIBITION; DISCOVERY; AFFINITY; PROTACS;
D O I
10.1016/j.cbpa.2020.12.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Targeted protein degradation offers several advantages over direct inhibition of protein activity and is gaining increasing interest in chemical biology and drug discovery. Proteolysis targeting chimeras (PROTACs) in particular are enjoying widespread application. However, PROTACs, which recruit an E3 ligase for degradation of a target protein, still suffer from certain challenges. These include a limited selection for E3 ligases on the one hand and the requirement for potent target binding on the other hand. Both issues restrict the target scope available for PROTACs. Degraders that covalently engage the target protein or the E3 ligase can potentially expand the pool of both targets and E3 ligases. Moreover, they may offer additional advantages by improving the kinetics of ternary complex formation or by endowing additional selectivity to the degrader. Here, we review the recent progress in the emerging field of covalent PROTACs.
引用
收藏
页码:24 / 33
页数:10
相关论文
共 68 条
  • [11] Drugging the 'undruggable' cancer targets
    Dang, Chi V.
    Reddy, E. Premkumar
    Shokat, Kevan M.
    Soucek, Laura
    [J]. NATURE REVIEWS CANCER, 2017, 17 (08) : 502 - 508
  • [12] Small molecule degraders of the hepatitis C virus protease reduce susceptibility to resistance mutations
    de Wispelaere, Melissanne
    Du, Guangyan
    Donovan, Katherine A.
    Zhang, Tinghu
    Eleuteri, Nicholas A.
    Yuan, Jingting C.
    Kalabathula, Joann
    Nowak, Radoslaw P.
    Fischer, Eric S.
    Gray, Nathanael S.
    Yang, Priscilla L.
    [J]. NATURE COMMUNICATIONS, 2019, 10 (1)
  • [13] Structural complementarity facilitates E7820-mediated degradation of RBM39 by DCAF15
    Faust, Tyler B.
    Yoon, Hojong
    Nowak, Radoslaw P.
    Donovan, Katherine A.
    Li, Zhengnian
    Cai, Quan
    Eleuteri, Nicholas A.
    Zhang, Tinghu
    Gray, Nathanael S.
    Fischer, Eric S.
    [J]. NATURE CHEMICAL BIOLOGY, 2020, 16 (01) : 7 - +
  • [14] Identification of the Clinical Development Candidate MRTX849, a Covalent KRASG12C Inhibitor for the Treatment of Cancer
    Fell, Jay B.
    Fischer, John P.
    Baer, Brian R.
    Blake, James F.
    Bouhana, Karyn
    Briere, David M.
    Brown, Karin D.
    Burgess, Laurence E.
    Burns, Aaron C.
    Burkard, Michael R.
    Chiang, Harrah
    Chicarelli, Mark J.
    Cook, Adam W.
    Gaudino, John J.
    Hallin, Jill
    Hanson, Lauren
    Hartley, Dylan P.
    Hicken, Erik J.
    Hingorani, Gary P.
    Hinklin, Ronald J.
    Mejia, Macedonio J.
    Olson, Peter
    Otten, Jennifer N.
    Rhodes, Susan P.
    Rodriguez, Martha E.
    Savechenkov, Pavel
    Smith, Darin J.
    Sudhakar, Niranjan
    Sullivan, Francis X.
    Tang, Tony P.
    Vigers, Guy P.
    Wollenberg, Lance
    Christensen, James G.
    Marx, Matthew A.
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2020, 63 (13) : 6679 - 6693
  • [15] Hitting KRAS When It's Down
    Gabizon, Ronen
    London, Nir
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2020, 63 (13) : 6677 - 6678
  • [16] Efficient Targeted Degradation via Reversible and Irreversible Covalent PROTACs
    Gabizon, Ronen
    Shraga, Amit
    Gehrtz, Paul
    Livnah, Ella
    Shorer, Yamit
    Gurwicz, Neta
    Avram, Liat
    Unger, Tamar
    Aharoni, Hila
    Albeck, Shira
    Brandis, Alexander
    Shulman, Ziv
    Katz, Ben-Zion
    Herishanu, Yair
    London, Nir
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2020, 142 (27) : 11734 - 11742
  • [17] Gadd MS, 2017, NAT CHEM BIOL, V13, P514, DOI [10.1038/NCHEMBIO.2329, 10.1038/nchembio.2329]
  • [18] MDM2-Recruiting PROTAC Offers Superior, Synergistic Antiproliferative Activity via Simultaneous Degradation of BRD4 and Stabilization of p53
    Hines, John
    Lartigue, Schan
    Dong, Hanqing
    Qian, Yimin
    Crews, Craig M.
    [J]. CANCER RESEARCH, 2019, 79 (01) : 251 - 262
  • [19] Manumycin polyketides act as molecular glues between UBR7 and P53
    Isobe, Yosuke
    Okumura, Mikiko
    McGregor, Lynn M.
    Brittain, Scott M.
    Jones, Michael D.
    Liang, Xiaoyou
    White, Ross
    Forrester, William
    McKenna, Jeffrey M.
    Tallarico, John A.
    Schirle, Markus
    Maimone, Thomas J.
    Nomura, Daniel K.
    [J]. NATURE CHEMICAL BIOLOGY, 2020, 16 (11) : 1189 - +
  • [20] Design, synthesis and biological evaluation of Proteolysis Targeting Chimeras (PROTACs) as a BTK degraders with improved pharmacokinetic properties
    Jaime-Figueroa, Saul
    Buhimschi, Alexandru D.
    Toure, Momar
    Hines, John
    Crews, Craig M.
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2020, 30 (03)