Rapid labelling and covalent inhibition of intracellular native proteins using ligand-directed N-acyl-N-alkyl sulfonamide
Chemically modifying proteins is hard to achieve selectively without purifying the target protein. Here, the authors present a method to modify proteins on lysine residues in living cells quicker than via known approaches and show that it can be used to develop protein covalent inhibitors.
Saved in:
Main Authors: | Tomonori Tamura, Tsuyoshi Ueda, Taiki Goto, Taku Tsukidate, Yonatan Shapira, Yuki Nishikawa, Alma Fujisawa, Itaru Hamachi |
---|---|
Format: | article |
Language: | EN |
Published: |
Nature Portfolio
2018
|
Subjects: | |
Online Access: | https://doaj.org/article/7cb4a42cb77f46bb9985a6f970724a6a |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
IONIC LIQUID-ACCELERATED SYNTHESIS OF SOME N-ALKYL DERIVATWES OF PHTHALIMIDE AND SULFONAMIDES
by: HASANINEJAD,ALIREZA, et al.
Published: (2008) -
Practical access to axially chiral sulfonamides and biaryl amino phenols via organocatalytic atroposelective N-alkylation
by: Shenci Lu, et al.
Published: (2019) -
SYNTHESIS OF 1-n-ALKYL-3-METHYL- AND 1-n-ALKYL-3- PHENYL-5-PYRAZOLONES AND FORMYL DERIVATIVES
by: BELMAR,J., et al.
Published: (2001) -
Synthesis and antiangiogenic activity of N-alkylated levamisole derivatives.
by: Anders N Hansen, et al.
Published: (2012) -
EXPERIMENTAL AND THEORETICAL STUDY OF SHYNTESIS OF N-ALKYL-NITROIMIDAZOLES.
by: Constain SALAMANCA M., et al.
Published: (2010)