Huntingtin Polyglutamine-Dependent Protein Aggregation in Reconstituted Cells

ACS Synth Biol. 2018 Feb 16;7(2):377-383. doi: 10.1021/acssynbio.7b00372. Epub 2017 Dec 14.

Abstract

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 polyQ-dependent 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.

Keywords: GUV; Huntingtin; cell-free protein synthesis; polyglutamine; protein aggregation; reconstitution.

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell-Free System / chemistry
  • Cell-Free System / metabolism
  • HeLa Cells
  • Humans
  • Huntingtin Protein* / chemistry
  • Huntingtin Protein* / genetics
  • Huntingtin Protein* / metabolism
  • Mutation*
  • Peptides* / chemistry
  • Peptides* / genetics
  • Peptides* / metabolism
  • Protein Aggregation, Pathological* / genetics
  • Protein Aggregation, Pathological* / metabolism
  • Unilamellar Liposomes* / chemistry
  • Unilamellar Liposomes* / metabolism

Substances

  • HTT protein, human
  • Huntingtin Protein
  • Peptides
  • Unilamellar Liposomes
  • polyglutamine