TY - JOUR
T1 - The development of modified human Hsp70 (HSPA1A) and its production in the milk of transgenic mice
AU - Gurskiy, Yaroslav G.
AU - Garbuz, David G.
AU - Soshnikova, Nataliya V.
AU - Krasnov, Aleksey N.
AU - Deikin, Alexei
AU - Lazarev, Vladimir F.
AU - Sverchinskyi, Dmitry
AU - Margulis, Boris A.
AU - Zatsepina, Olga G.
AU - Karpov, Vadim L.
AU - Belzhelarskaya, Svetlana N.
AU - Feoktistova, Evgenia
AU - Georgieva, Sofia G.
AU - Evgen’ev, Michael B.
N1 - Publisher Copyright:
© 2016, Cell Stress Society International.
PY - 2016/11/1
Y1 - 2016/11/1
N2 - The production of major human heat shock protein Hsp70 (HSPA1A) in a eukaryotic expression system is needed for testing and possible medical applications. In this study, transgenic mice were produced containing wild-type human Hsp70 allele in the vector providing expression in the milk. The results indicated that human Hsp70 was readily expressed in the transgenic animals but did not apparently preserve its intact structure and, hence, it was not possible to purify the protein using conventional isolation techniques. It was suggested that the protein underwent glycosylation in the process of expression, and this quite common modification for proteins expressed in the milk complicated its isolation. To check this possibility, we mutated all presumptive sites of glycosylation and tested the properties of the resulting modified Hsp70 expressed in E. coli. The investigation demonstrated that the modified protein exhibited all beneficial properties of the wild-type Hsp70 and was even superior to the latter for a few parameters. Based on these results, a transgenic mouse strain was obtained which expressed the modified Hsp70 in milk and which was easy to isolate using ATP columns. Therefore, the developed construct can be explored in various bioreactors for reliable manufacture of high quality, uniform, and reproducible human Hsp70 for possible medical applications including neurodegenerative diseases and cancer.
AB - The production of major human heat shock protein Hsp70 (HSPA1A) in a eukaryotic expression system is needed for testing and possible medical applications. In this study, transgenic mice were produced containing wild-type human Hsp70 allele in the vector providing expression in the milk. The results indicated that human Hsp70 was readily expressed in the transgenic animals but did not apparently preserve its intact structure and, hence, it was not possible to purify the protein using conventional isolation techniques. It was suggested that the protein underwent glycosylation in the process of expression, and this quite common modification for proteins expressed in the milk complicated its isolation. To check this possibility, we mutated all presumptive sites of glycosylation and tested the properties of the resulting modified Hsp70 expressed in E. coli. The investigation demonstrated that the modified protein exhibited all beneficial properties of the wild-type Hsp70 and was even superior to the latter for a few parameters. Based on these results, a transgenic mouse strain was obtained which expressed the modified Hsp70 in milk and which was easy to isolate using ATP columns. Therefore, the developed construct can be explored in various bioreactors for reliable manufacture of high quality, uniform, and reproducible human Hsp70 for possible medical applications including neurodegenerative diseases and cancer.
KW - Escherichia coli
KW - Glycosylation
KW - Heat shock protein 70
KW - Site-directed mutagenesis
KW - Transgenic mice
UR - http://www.scopus.com/inward/record.url?scp=84981249226&partnerID=8YFLogxK
U2 - 10.1007/s12192-016-0729-x
DO - 10.1007/s12192-016-0729-x
M3 - Article
C2 - 27511022
AN - SCOPUS:84981249226
SN - 1355-8145
VL - 21
SP - 1055
EP - 1064
JO - Cell Stress and Chaperones
JF - Cell Stress and Chaperones
IS - 6
ER -