Dessev G, Iovcheva C, Tasheva B, Goldman R
Department of Cell Biology and Anatomy, Northwestern University Medical School, Chicago, IL 60611.
Proc Natl Acad Sci U S A. 1988 May;85(9):2994-8. doi: 10.1073/pnas.85.9.2994.
A nuclear lamina-enriched fraction from Ehrlich ascites tumor cells contains a tightly bound protein kinase activity, which phosphorylates in vitro the nuclear lamins, a 52-kilodalton protein, and several unknown minor components. The enzyme(s) is thermolabile, independent of Ca2+ and cAMP, and inhibited by quercetin. After treatment with 4 M urea it remains bound to the nuclear lamina in an active state, but it is irreversibly inactivated in 6 M urea. The lamin proteins are phosphorylated on serine residues. Their two-dimensional phosphopeptide maps show multiple phosphorylation sites and a considerable similarity to the phosphopeptide maps of lamins labeled in vivo. Photoaffinity labeling experiments revealed several polypeptide fractions in the nuclear lamina fraction that are candidates for the protein kinase(s).
艾氏腹水瘤细胞核纤层富集组分含有紧密结合的蛋白激酶活性,该活性在体外可使核纤层蛋白、一种52千道尔顿的蛋白质以及几种未知的次要成分发生磷酸化。该酶不耐热,不依赖Ca2+和cAMP,并受槲皮素抑制。用4M尿素处理后,它仍以活性状态与核纤层结合,但在6M尿素中会不可逆地失活。核纤层蛋白在丝氨酸残基上发生磷酸化。它们的二维磷酸肽图谱显示有多个磷酸化位点,且与体内标记的核纤层蛋白的磷酸肽图谱有相当的相似性。光亲和标记实验揭示了核纤层组分中的几个多肽组分,它们可能是该蛋白激酶的候选物。