TY - JOUR
T1 - Chemical chromatin ubiquitylation
AU - Jbara, Muhammad
AU - Sun, Hao
AU - Kamnesky, Guy
AU - Brik, Ashraf
N1 - Publisher Copyright:
© 2018 Elsevier Ltd
PY - 2018/8
Y1 - 2018/8
N2 - Histone modifications dynamically regulate chromatin structure and function, thereby mediating many processes that require access to DNA. Chemical protein synthesis has emerged as a powerful approach for generating homogeneously modified histone analogues in workable amounts for subsequent incorporation into nucleosome arrays for biochemical, functional and structural studies. This short review focuses on the strength of total chemical protein synthesis and semisynthetic approaches to generate ubiquitylated histones in their native or non-native forms and the utility of these analogues to decode the role of ubiquitylation in epigenetics.
AB - Histone modifications dynamically regulate chromatin structure and function, thereby mediating many processes that require access to DNA. Chemical protein synthesis has emerged as a powerful approach for generating homogeneously modified histone analogues in workable amounts for subsequent incorporation into nucleosome arrays for biochemical, functional and structural studies. This short review focuses on the strength of total chemical protein synthesis and semisynthetic approaches to generate ubiquitylated histones in their native or non-native forms and the utility of these analogues to decode the role of ubiquitylation in epigenetics.
UR - http://www.scopus.com/inward/record.url?scp=85042267401&partnerID=8YFLogxK
U2 - 10.1016/j.cbpa.2018.02.001
DO - 10.1016/j.cbpa.2018.02.001
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.systematicreview???
C2 - 29459258
AN - SCOPUS:85042267401
SN - 1367-5931
VL - 45
SP - 18
EP - 26
JO - Current Opinion in Chemical Biology
JF - Current Opinion in Chemical Biology
ER -