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  • Nopp140  (1)
  • Phosphorylation  (1)
  • Sf-9 cells  (1)
  • cyclic AMP-dependent protein kinase  (1)
  • growth factors  (1)
Material
Years
Keywords
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Molecular and cellular biochemistry 191 (1999), S. 223-228 
    ISSN: 1573-4919
    Keywords: protein kinase CK2 ; nucleolin ; IRS-1 ; Nopp140 ; overlay methods
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract In order to aid in an understanding of the cellular functions of protein kinase CK2, a search for interacting proteins was carried out using a 32P-labeled CK2 overlay method. Several proteins were found to associate with CK2 by this assay; among them, one protein of 110 kDa appeared to be the most prominent one. The possible association of CK2 with p110 was suggested by experiments involving the co-immunoprecipitation using anti-CK2 antibodies. Further analysis using GST-CK2 fusion proteins demonstrated that the CK2-p110 interaction occurred through the CK2α/α′ subunits. To identify p110, it was purified using a GST-CK2 affinity column, and internal amino acid sequencing was then performed. p110 was found to be nucleolin, a nucleolar protein that may be important for rRNA synthesis; a possible role of CK2 in the control of this process is suggested. Using the same CK2 overlay technique, another interacting protein, insulin receptor substrate 1 (IRS-1), was also identified. By applying a modified overlay method using individual 35S-labeled CK2 subunits, obtained by in vitro translation in rabbit reticulate lysates, it was determined that CK2 associates with IRS-1 through its α/α′ subunits; i.e. in keeping with the fact that IRS-1 is a known substrate for CK2. However, further work is needed to examine the association of CK2 with IRS-1 in vivo in order to fully understand the significance of the interaction.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Molecular and cellular biochemistry 191 (1999), S. 3-12 
    ISSN: 1573-4919
    Keywords: protein kinase CK2 ; Sf-9 cells ; baculovirus expression system ; autophosphorylation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Protein kinase CK2 is a ubiquitous eukaryotic protein kinase composed of two catalytic subunits, α and/or α′, and two regulatory subunits, β. In order to define similarities and dissimilarities between the α and α ′ catalytic subunits, which might account for their particular cellular functions, different forms of the enzyme were expressed in Sf9 cells and their properties determined. Both catalytic subunits were expressed separately, and also along with the regulatory β subunit, in order to obtain free α and α′, as well as α2β2 and α′2β2 forms. Our results confirm that the b subunit acts to stabilize the α and α′ subunits and also influences the substrate specificity and kinetic properties of the enzyme. Although significant differences between the specificities of holoenzymes α2β2 and α′2β2 as determined using a number of substrates were not detected, autophosphorylation studies on α2β2 and α′2β2 revealed significant differences in this property. The regulatory subunit β was phosphorylated less rapidly by the α′ subunit than by the α subunit, and the extent of phosphorylation of β by α was also greater than that of β by α′. It was also noted that the thermo-stability and the extent of its activation by NaCl were greater for αβ2 than for α′β2. These different properties may relate to distinct functions of the two form of CK2.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Bioscience reports 13 (1993), S. 127-142 
    ISSN: 1573-4935
    Keywords: protein phosphorylation ; protein kinase ; phosphorylase ; glycogen metabolism ; normonal signaling ; cyclic AMP ; cyclic AMP-dependent protein kinase ; insulin ; growth factors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 32 (1993), S. 1122-1129 
    ISSN: 0570-0833
    Keywords: Proteins ; Phosphorylation ; Cellular regulation ; Nobel lecture ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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