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Quantitative analysis of PPT1 interactome in human neuroblastoma cells.
Scifo, Enzo; Szwajda, Agnieszka; Soliymani, Rabah; Pezzini, Francesco; Bianchi, Marzia; Dapkunas, Arvydas; Debski, Janusz; Uusi-Rauva, Kristiina; Dadlez, Michal; Gingras, Anne-Claude; Tyynelä, Jaana; Simonati, Alessandro; Jalanko, Anu; Baumann, Marc H; Lalowski, Maciej.
Afiliação
  • Scifo E; Meilahti Clinical Proteomics Core Facility, Institute of Biomedicine, Biochemistry and Developmental Biology, University of Helsinki, Helsinki, Finland ; Doctoral Program Brain & Mind, University of Helsinki, Helsinki, Finland.
  • Szwajda A; Institute for Molecular Medicine (FIMM), University of Helsinki, Helsinki, Finland.
  • Soliymani R; Meilahti Clinical Proteomics Core Facility, Institute of Biomedicine, Biochemistry and Developmental Biology, University of Helsinki, Helsinki, Finland.
  • Pezzini F; Department of Neurological and Movement Sciences, University of Verona, Verona, Italy.
  • Bianchi M; Department of Neurological and Movement Sciences, University of Verona, Verona, Italy ; Unit for Neuromuscular and Neurodegenerative Disorders, Laboratory of Molecular Medicine, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Dapkunas A; Meilahti Clinical Proteomics Core Facility, Institute of Biomedicine, Biochemistry and Developmental Biology, University of Helsinki, Helsinki, Finland.
  • Debski J; Mass Spectrometry Laboratory, Department of Biophysics, Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland.
  • Uusi-Rauva K; Folkhälsan Institute of Genetics, Helsinki, Finland ; National Institute for Health and Welfare, Public Health Genomics Unit, Helsinki, Finland.
  • Dadlez M; Mass Spectrometry Laboratory, Department of Biophysics, Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland.
  • Gingras AC; Centre for Systems Biology, Samuel Lunenfeld Research Institute at Mount Sinai Hospital, Toronto, and Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada.
  • Tyynelä J; Meilahti Clinical Proteomics Core Facility, Institute of Biomedicine, Biochemistry and Developmental Biology, University of Helsinki, Helsinki, Finland.
  • Simonati A; Department of Neurological and Movement Sciences, University of Verona, Verona, Italy.
  • Jalanko A; Institute for Molecular Medicine (FIMM), University of Helsinki, Helsinki, Finland ; National Institute for Health and Welfare, Public Health Genomics Unit, Helsinki, Finland.
  • Baumann MH; Meilahti Clinical Proteomics Core Facility, Institute of Biomedicine, Biochemistry and Developmental Biology, University of Helsinki, Helsinki, Finland.
  • Lalowski M; Meilahti Clinical Proteomics Core Facility, Institute of Biomedicine, Biochemistry and Developmental Biology, University of Helsinki, Helsinki, Finland ; Folkhälsan Institute of Genetics, Helsinki, Finland.
Data Brief ; 4: 207-16, 2015 Sep.
Article em En | MEDLINE | ID: mdl-26217791
Mutations in the CLN1 gene that encodes Palmitoyl protein thioesterase 1 (PPT1) or CLN1, cause Infantile NCL (INCL, MIM#256730). PPT1 removes long fatty acid chains such as palmitate from modified cysteine residues of proteins. The data shown here result from isolated protein complexes from PPT1-expressing SH-SY5Y stable cells that were subjected to single step affinity purification coupled to mass spectrometry (AP-MS). Prior to the MS analysis, we utilised a modified filter-aided sample preparation (FASP) protocol. Based on label free quantitative analysis of the data by SAINT, 23 PPT1 interacting partners (IP) were identified. A dense connectivity in PPT1 network was further revealed by functional coupling and extended network analyses, linking it to mitochondrial ATP synthesis coupled protein transport and thioester biosynthetic process. Moreover, the terms: inhibition of organismal death, movement disorders and concentration of lipid were predicted to be altered in the PPT1 network. Data presented here are related to Scifo et al. (J. Proteomics, 123 (2015) 42-53).

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Finlândia

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Finlândia