LEE, VING J.;CURRAN, WILLIAM V.;FIELDS, THOMAS F.;LEARN, KEITH, J. HETEROCYCL. CHEM., 25,(1988) N, C. 1873-1891
作者:LEE, VING J.、CURRAN, WILLIAM V.、FIELDS, THOMAS F.、LEARN, KEITH
DOI:——
日期:——
TUNABLE ENDOGENOUS PROTEIN DEGRADATION
申请人:Dana-Farber Cancer Institute, Inc.
公开号:US20180179522A1
公开(公告)日:2018-06-28
The present invention provides a means to modulate gene expression in vivo in a manner that avoids problems associated with CRISPR endogenous protein knock-out or knock-in strategies and strategies that provide for correction, or alteration, of single nucleotides. The invention includes inserting into the genome a nucleotide encoding a heterobifunctional compound targeting protein (dTAG) in-frame with the nucleotide sequence of a gene encoding an endogenously expressed protein of interest which, upon expression, produces an endogenous protein-dTAG hybrid protein. This allows for targeted protein degradation of the dTAG and the fused endogenous protein using a heterobifunctional compound.
Lee, Ving J.; Curran, William V.; Fields, Thomas F., Journal of Heterocyclic Chemistry, 1988, vol. 25, p. 1873 - 1891
作者:Lee, Ving J.、Curran, William V.、Fields, Thomas F.、Learn, Keith