Wang D S, Miller R, Shaw R, Shaw G
Department of Neuroscience, University of Florida College of Medicine, Gainesville 32610, USA.
Biochem Biophys Res Commun. 1996 Aug 14;225(2):420-6. doi: 10.1006/bbrc.1996.1189.
We have examined the in vivo targeting potential of the Pleckstrin Homology (PH) domain from human beta I sigma II spectrin using a novel Aequoria victoria green fluorescent protein (GFP) fusion vector constructed from a human codon optimized cDNA. This vector efficiently expresses both GFP and the GFP spectrin fusion protein in COS7 and other cell lines. GFP expressed alone shows only diffuse cytoplasmic staining which is not associated with the plasma membrane. In contrast the GFP-beta I sigma II spectrin PH domain fusion protein localizes under the plasma membrane of transfected COS7 cells in vivo. Fixation of cells transfected with GFP alone in -20 degrees C methanol results in the removal of all specific fluorescence. In contrast cells transfected with the GFP-beta I sigma II spectrin construct and fixed -20 degrees C methanol continue to show strong membrane fluorescence, consistent with a role for the spectrin PH domain in membrane localization in vivo.
我们使用一种由人密码子优化的cDNA构建的新型维多利亚水母绿色荧光蛋白(GFP)融合载体,研究了人βIσII血影蛋白的普列克底物同源(PH)结构域的体内靶向潜力。该载体在COS7和其他细胞系中高效表达GFP和GFP血影蛋白融合蛋白。单独表达的GFP仅显示弥漫性细胞质染色,与质膜无关。相比之下,GFP-βIσII血影蛋白PH结构域融合蛋白在体内定位于转染的COS7细胞质膜下。用-20℃甲醇固定单独转染GFP的细胞会导致所有特异性荧光消失。相比之下,用GFP-βIσII血影蛋白构建体转染并用-20℃甲醇固定的细胞继续显示强烈的膜荧光,这与血影蛋白PH结构域在体内膜定位中的作用一致。