Huntingtin Polyglutamine-Dependent Protein Aggregation in Reconstituted Cells

被引:6
|
作者
Machida, Kodai [1 ,2 ]
Kanzawa, Kuru [1 ]
Shigeta, Tomoaki [1 ]
Yamamoto, Yuki [1 ]
Tsumoto, Kanta [3 ]
Imataka, Hiroaki [1 ,2 ]
机构
[1] Univ Hyogo, Grad Sch Engn, Dept Appl Chem, Himeji, Hyogo 6712201, Japan
[2] RIKEN, Ctr Life Sci Technol, Yokohama, Kanagawa 2300045, Japan
[3] Mie Univ, Grad Sch Engn, Div Chem Mat, Tsu, Mie 5148507, Japan
来源
ACS SYNTHETIC BIOLOGY | 2018年 / 7卷 / 02期
关键词
cell-free protein synthesis; GUV; Huntingtin; polyglutamine; protein aggregation; reconstitution; IN-VITRO EVOLUTION; FLANKING SEQUENCES; LIPOSOME DISPLAY; TRANSLATION; TOXICITY; SYSTEM; VESICLES; DISEASE; ABCE1;
D O I
10.1021/acssynbio.7b00372
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
One of the aims of synthetic biology is bottom-up construction of reconstituted human cells for medical uses. To that end, we generated giant unilamellar vesicles (GUVs) that contained a HeLa cell extract, which comprises a cell-free protein synthesis (CFPS) system. Then we expressed Huntingtin protein fragments that contained polyglutamine (polyQ) sequences (Htt-polyQ), a hallmark of Huntington's disease. That system produced polyQdependent protein aggregates, as previously demonstrated in living cells. We next simplified the system by generating GUVs that contained purified human factors, which reconstituted a CFPS system. Htt-polyQ fragments expressed in these GUVs also formed protein aggregates. Moreover, an N-terminal deletion mutant, which had failed to form protein aggregates in living cells, also failed to form protein aggregates in the reconstituted GUVs. Thus, the GUV systems that encapsulated a human CFPS system could serve as reconstituted cells for studying neurological diseases.
引用
收藏
页码:377 / 383
页数:13
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