Chemically induced proximity in biology and medicine

被引:299
作者
Stanton, Benjamin Z. [1 ,2 ,3 ]
Chory, Emma J. [1 ,2 ,4 ]
Crabtree, Gerald R. [1 ,2 ,5 ]
机构
[1] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
[3] Natl Ctr Adv Translat Sci, Div Preclin Innovat, NIH, Rockville, MD 20850 USA
[4] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
[5] Stanford Univ, Howard Hughes Med Inst, Sch Med, Stanford, CA 94305 USA
关键词
E3 UBIQUITIN LIGASE; BET BROMODOMAIN INHIBITION; ARTIFICIAL DEATH SWITCHES; SMALL-MOLECULE PROTACS; STEM-CELL TRANSPLANT; IN-VIVO; T-CELLS; LIVING CELLS; ENDOPLASMIC-RETICULUM; INDUCED DIMERIZATION;
D O I
10.1126/science.aao5902
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
Proximity, or the physical closeness of molecules, is a pervasive regulatory mechanism in biology. For example, most posttranslational modifications such as phosphorylation, methylation, and acetylation promote proximity of molecules to play deterministic roles in cellular processes. To understand the role of proximity in biologic mechanisms, chemical inducers of proximity (CIPs) were developed to synthetically model biologically regulated recruitment. Chemically induced proximity allows for precise temporal control of transcription, signaling cascades, chromatin regulation, protein folding, localization, and degradation, as well as a host of other biologic processes. A systematic analysis of CIPs in basic research, coupled with recent technological advances utilizing CRISPR, distinguishes roles of causality from coincidence and allows for mathematical modeling in synthetic biology. Recently, induced proximity has provided new avenues of gene therapy and emerging advances in cancer treatment.
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页数:9
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