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Adenylated proteins in mouse B16-F10 melanoma cells cluster in functional categories: a new paradigm for cellular regulation?
Fatima, Narjis; Alomari, Munther; Belov, Larissa; Shen, Yandong; Christopherson, Richard I.
Afiliação
  • Fatima N; School of Life and Environmental Sciences, University of Sydney, Sydney, NSW, Australia.
  • Alomari M; School of Life and Environmental Sciences, University of Sydney, Sydney, NSW, Australia.
  • Belov L; Present address: Department of Stem Cells, Institute for Research and Medical Consultations (IRMC), Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.
  • Shen Y; School of Life and Environmental Sciences, University of Sydney, Sydney, NSW, Australia.
  • Christopherson RI; School of Life and Environmental Sciences, University of Sydney, Sydney, NSW, Australia.
Article em En | MEDLINE | ID: mdl-34738868
ABSTRACT
In mammals, AMPylation of cellular proteins is carried out by Huntingtin yeast-interacting protein E, and pseudokinase SelO. Lysates from mouse B16-F10 melanoma cells have been fractionated by immuno-precipitation using magnetic Dynabeads coated with antibodies against both adenosine 5'-monophosphate in phosphate ester linkage to tyrosine, and adenosine-phosphate. Proteins pulled down with both these antibodies were subject to post-translational modification, most likely AMPylation. Using tandem mass spectrometry, analysis of these protein fractions identified 333 proteins that could be pulled down by both antibodies. Many of these proteins clustered in 13 functional Ingenuity Pathway Analysis categories of 4 or more adenylated proteins including some from the cytoskeleton, and some involved with initiating the unfolded protein response.Supplemental data for this article is available online at https//doi.org/10.1080/15257770.2021.1995608 .
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article