TY - JOUR
T1 - Use of the LC3B-fusion technique for biochemical and structural studies of proteins involved in the N-degron pathway
AU - Kim, Leehyeon
AU - Kwon, Do Hoon
AU - Heo, Jiwon
AU - Park, Mi Rae
AU - Song, Hyun Kyu
N1 - Funding Information:
This work was supported in part by a Korean University Grant and by Sam-sung Science & Technology Foundation Grant SSTF-BA 1701-14. The authors declare that they have no conflicts of interest with the contents of this article.
Publisher Copyright:
© 2020 Kim et al.
PY - 2020/2/28
Y1 - 2020/2/28
N2 - The N-degron pathway, formerly the N-end rule pathway, is a protein degradation process that determines the half-life of proteins based on their N-terminal residues. In contrast to the wellestablished in vivo studies over decades, in vitro studies of this pathway, including biochemical characterization and high-resolution structures, are relatively limited. In this study, we have developed a unique fusion technique using microtubule-associated protein1A/1Blight chain 3B, a key marker protein of autophagy, to tag the N terminus of the proteins involved in the N-degron pathway, which enables high yield ofhomogeneoustarget proteins with variable N-terminal residues for diverse biochemical studies including enzymatic and binding assays and substrate identification. Intriguingly, crystallization showed a markedly enhanced probability, even for the N-degron complexes.Tovalidate our results,wedetermined the structures of select proteins in the N-degron pathway and compared them with the Protein Data Bank-deposited proteins. Furthermore, several biochemical applications of this technique were introduced. Therefore, this technique can be used as a general tool for the in vitro study of the N-degron pathway.
AB - The N-degron pathway, formerly the N-end rule pathway, is a protein degradation process that determines the half-life of proteins based on their N-terminal residues. In contrast to the wellestablished in vivo studies over decades, in vitro studies of this pathway, including biochemical characterization and high-resolution structures, are relatively limited. In this study, we have developed a unique fusion technique using microtubule-associated protein1A/1Blight chain 3B, a key marker protein of autophagy, to tag the N terminus of the proteins involved in the N-degron pathway, which enables high yield ofhomogeneoustarget proteins with variable N-terminal residues for diverse biochemical studies including enzymatic and binding assays and substrate identification. Intriguingly, crystallization showed a markedly enhanced probability, even for the N-degron complexes.Tovalidate our results,wedetermined the structures of select proteins in the N-degron pathway and compared them with the Protein Data Bank-deposited proteins. Furthermore, several biochemical applications of this technique were introduced. Therefore, this technique can be used as a general tool for the in vitro study of the N-degron pathway.
UR - http://www.scopus.com/inward/record.url?scp=85080865981&partnerID=8YFLogxK
U2 - 10.1074/jbc.RA119.010912
DO - 10.1074/jbc.RA119.010912
M3 - Article
C2 - 31919097
AN - SCOPUS:85080865981
SN - 0021-9258
VL - 295
SP - 2590
EP - 2600
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 9
ER -