共 122 条
Targeting the undruggables-the power of protein degraders
被引:31
作者:

Zhang, Chao
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h-index: 0
机构:
Changping Lab, Beijing 102206, Peoples R China Tsinghua Univ, MOE Key Lab Prot Sci, Sch Pharmaceut Sci,State Key Lab Mol Oncol, MOE Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China

Liu, Yongbo
论文数: 0 引用数: 0
h-index: 0
机构:
Tsinghua Univ, MOE Key Lab Prot Sci, Sch Pharmaceut Sci,State Key Lab Mol Oncol, MOE Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China Tsinghua Univ, MOE Key Lab Prot Sci, Sch Pharmaceut Sci,State Key Lab Mol Oncol, MOE Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China

Li, Guangchen
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h-index: 0
机构:
Tsinghua Univ, MOE Key Lab Prot Sci, Sch Pharmaceut Sci,State Key Lab Mol Oncol, MOE Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China Tsinghua Univ, MOE Key Lab Prot Sci, Sch Pharmaceut Sci,State Key Lab Mol Oncol, MOE Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China

Yang, Zhouli
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Tsinghua Univ, MOE Key Lab Prot Sci, Sch Pharmaceut Sci,State Key Lab Mol Oncol, MOE Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China Tsinghua Univ, MOE Key Lab Prot Sci, Sch Pharmaceut Sci,State Key Lab Mol Oncol, MOE Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China

Han, Chi
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机构:
Tsinghua Univ, MOE Key Lab Prot Sci, Sch Pharmaceut Sci,State Key Lab Mol Oncol, MOE Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China Tsinghua Univ, MOE Key Lab Prot Sci, Sch Pharmaceut Sci,State Key Lab Mol Oncol, MOE Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China

Sun, Xiuyun
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机构:
Changping Lab, Beijing 102206, Peoples R China Tsinghua Univ, MOE Key Lab Prot Sci, Sch Pharmaceut Sci,State Key Lab Mol Oncol, MOE Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China

Sheng, Chunquan
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机构:
Second Mil Med Univ, Sch Pharm, Shanghai 200433, Peoples R China Tsinghua Univ, MOE Key Lab Prot Sci, Sch Pharmaceut Sci,State Key Lab Mol Oncol, MOE Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China

Ding, Ke
论文数: 0 引用数: 0
h-index: 0
机构:
Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Chem Biol, Shanghai 200032, Peoples R China Tsinghua Univ, MOE Key Lab Prot Sci, Sch Pharmaceut Sci,State Key Lab Mol Oncol, MOE Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China

Rao, Yu
论文数: 0 引用数: 0
h-index: 0
机构:
Tsinghua Univ, MOE Key Lab Prot Sci, Sch Pharmaceut Sci,State Key Lab Mol Oncol, MOE Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China
Changping Lab, Beijing 102206, Peoples R China Tsinghua Univ, MOE Key Lab Prot Sci, Sch Pharmaceut Sci,State Key Lab Mol Oncol, MOE Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China
机构:
[1] Tsinghua Univ, MOE Key Lab Prot Sci, Sch Pharmaceut Sci,State Key Lab Mol Oncol, MOE Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China
[2] Changping Lab, Beijing 102206, Peoples R China
[3] Second Mil Med Univ, Sch Pharm, Shanghai 200433, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Chem Biol, Shanghai 200032, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Undruggables;
Targeted protein degradation;
PROTAC;
Molecule glue;
DAC;
LYTAC;
SELECTIVE DEGRADATION;
CYCLOSPORINE-A;
IN-VIVO;
PROMOTES;
CANCER;
GSPT1;
DRUG;
DISCOVERY;
COMPLEX;
D O I:
10.1016/j.scib.2024.03.056
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Undruggable targets typically refer to a class of therapeutic targets that are difficult to target through conventional methods or have not yet been targeted, but are of great clinical significance. According to statistics, over 80% of disease -related pathogenic proteins cannot be targeted by current conventional treatment methods. In recent years, with the advancement of basic research and new technologies, the development of various new technologies and mechanisms has brought new perspectives to overcome challenging drug targets. Among them, targeted protein degradation technology is a breakthrough drug development strategy for challenging drug targets. This technology can specifically identify target proteins and directly degrade pathogenic target proteins by utilizing the inherent protein degradation pathways within cells. This new form of drug development includes various types such as proteolysis targeting chimera (PROTAC), molecular glue, lysosome-targeting Chimaera (LYTAC), autophagosometethering compound (ATTEC), autophagy-targeting chimera (AUTAC), autophagy-targeting chimera (AUTOTAC), degrader -antibody conjugate (DAC). This article systematically summarizes the application of targeted protein degradation technology in the development of degraders for challenging drug targets. Finally, the article looks forward to the future development direction and application prospects of targeted protein degradation technology. (c) 2024 Science China Press. Published by Elsevier B.V. and Science China Press. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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页码:1776 / 1797
页数:22
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Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06511 USA Yale Univ, Dept Pharmacol, New Haven, CT 06511 USA

Crews, Craig M.
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机构:
Yale Univ, Dept Pharmacol, Dept Mol Cellular & Dev Biol, New Haven, CT 06511 USA
Yale Univ, Dept Chem, New Haven, CT 06511 USA Yale Univ, Dept Pharmacol, New Haven, CT 06511 USA