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Purification of full-length recombinant human huntingtin proteins with allelic series of polyglutamine lengths.
Kim, Hyeongju; Hyun, Kyung-Gi; Lloret, Alejandro; Seong, Ihn Sik; Song, Ji-Joon.
Afiliação
  • Kim H; Department of Biological Sciences, KI for the BioCentury, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, South Korea.
  • Hyun KG; Molecular Neurogenetics Unit, Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA 02114, USA.
  • Lloret A; Department of Neurology, Harvard Medical School, Boston, MA 02114, USA.
  • Seong IS; Molecular Neurogenetics Unit, Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA 02114, USA.
  • Song JJ; Department of Neurology, Harvard Medical School, Boston, MA 02114, USA.
STAR Protoc ; 2(4): 100886, 2021 12 17.
Article em En | MEDLINE | ID: mdl-34746859
Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder caused by the polyglutamine (polyQ) expansion in huntingtin (HTT) protein. The challenge of obtaining full-length HTT proteins with high purity limits the understanding of the HTT protein function. Here, we provide a protocol to generate and purify full-length recombinant human HTT proteins with various polyQ lengths, which is key to investigate the biochemical function of HTT proteins and the molecular mechanism underlying HD pathology. For complete details on the use and execution of this protocol, please refer to Jung et al. (2020).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peptídeos / Proteínas Recombinantes / Proteína Huntingtina Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peptídeos / Proteínas Recombinantes / Proteína Huntingtina Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article