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
相关论文
共 50 条
  • [21] Leuprorelin rescues polyglutamine-dependent phenotypes in a transgenic mouse model of spinal and bulbar muscular atrophy
    Katsuno, M
    Adachi, H
    Doyu, M
    Minamiyama, M
    Sang, C
    Kobayashi, Y
    Inukai, A
    Sobue, G
    NATURE MEDICINE, 2003, 9 (06) : 768 - 773
  • [22] Leuprorelin rescues polyglutamine-dependent phenotypes in a transgenic mouse model of spinal and bulbar muscular atrophy
    Masahisa Katsuno
    Hiroaki Adachi
    Manabu Doyu
    Makoto Minamiyama
    Chen Sang
    Yasushi Kobayashi
    Akira Inukai
    Gen Sobue
    Nature Medicine, 2003, 9 : 768 - 773
  • [23] Aggregation of huntingtin in yeast varies with the length of the polyglutamine expansion and the expression of chaperone proteins
    Krobitsch, S
    Lindquist, S
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (04) : 1589 - 1594
  • [24] Membrane Interactions Accelerate the Self-Aggregation of Huntingtin Exon 1 Fragments in a Polyglutamine Length-Dependent Manner
    Marquette, Arnaud
    Aisenbrey, Christopher
    Bechinger, Burkhard
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (13)
  • [25] Polyglutamine diseases: protein cleavage and aggregation
    Zoghbi, HY
    Orr, HT
    CURRENT OPINION IN NEUROBIOLOGY, 1999, 9 (05) : 566 - 570
  • [26] Forms and Phases in Huntingtin Protein Aggregation
    Elbaum, Michael
    MOLECULAR CELL, 2018, 70 (04) : 567 - 568
  • [27] Huntingtin toxicity in yeast model depends on polyglutamine aggregation mediated by a prion-like protein Rnq1
    Meriin, AB
    Zhang, XQ
    He, XW
    Newnam, GP
    Chernoff, YO
    Sherman, MY
    JOURNAL OF CELL BIOLOGY, 2002, 157 (06): : 997 - 1004
  • [28] Huntingtin affinity for partners is not changed by polyglutamine length: aggregation itself triggers aberrant interactions
    Davranche, Aurelien
    Aviolat, Hubert
    Zeder-Lutz, Gabrielle
    Busso, Didier
    Altschuh, Daniele
    Trottier, Yvon
    Klein, Fabrice A. C.
    HUMAN MOLECULAR GENETICS, 2011, 20 (14) : 2795 - 2806
  • [29] Polyglutamine disruption of the huntingtin exon 1 N terminus triggers a complex aggregation mechanism
    Ashwani K Thakur
    Murali Jayaraman
    Rakesh Mishra
    Monika Thakur
    Veronique M Chellgren
    In-Ja L Byeon
    Dalaver H Anjum
    Ravindra Kodali
    Trevor P Creamer
    James F Conway
    Angela M Gronenborn
    Ronald Wetzel
    Nature Structural & Molecular Biology, 2009, 16 : 380 - 389
  • [30] Polyglutamine disruption of the huntingtin exon 1 N terminus triggers a complex aggregation mechanism
    Thakur, Ashwani K.
    Jayaraman, Murali
    Mishra, Rakesh
    Thakur, Monika
    Chellgren, Veronique M.
    Byeon, In-Ja L.
    Anjum, Dalaver H.
    Kodali, Ravindra
    Creamer, Trevor P.
    Conway, James F.
    Gronenborn, Angela M.
    Wetzel, Ronald
    NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2009, 16 (04) : 380 - 389