Kruger K E, Sossin W S, Sacktor T C, Bergold P J, Beushausen S, Schwartz J H
Howard Hughes Medical Institute, Columbia University, New York, New York 10032.
J Neurosci. 1991 Aug;11(8):2303-13. doi: 10.1523/JNEUROSCI.11-08-02303.1991.
We isolated cDNA clones from an Aplysia sensory-cell library encoding two isoforms of protein kinase C (PKC). Several isozyme-specific regions are conserved in the Aplysia kinases, notably the variable regions V5 in the Ca(2+)-dependent PKC (Apl I) and V1 in the Ca(2+)-independent PKC (Apl II). Neuronal proteins with the properties expected of these two isoforms can be identified with antibodies raised against peptides synthesized from the amino acid sequences deduced from the clones. Sacktor and Schwartz (1990) measured the proportion of kinase activity that can be translocated to membrane in Aplysia sensory neurons and ganglia by stimuli that produce the presynaptic facilitation underlying behavioral sensitization. Much less Apl I and Apl II are translocated, suggesting that still other isoforms of PKC exist in these cells.
我们从海兔感觉细胞文库中分离出编码蛋白激酶C(PKC)两种同工型的cDNA克隆。海兔激酶中几个同工酶特异性区域是保守的,特别是依赖钙的PKC(Apl I)中的可变区V5和不依赖钙的PKC(Apl II)中的V1。具有这两种同工型预期特性的神经元蛋白可以用针对从克隆推导的氨基酸序列合成的肽产生的抗体来鉴定。萨克托和施瓦茨(1990年)测量了在海兔感觉神经元和神经节中可通过产生行为敏感化基础的突触前易化的刺激转移到膜上的激酶活性比例。转移的Apl I和Apl II少得多,这表明这些细胞中还存在PKC的其他同工型。