Dyer J M, Mullen R T
USDA-ARS Southern Regional Research Center, New Orleans, LA 70124, USA.
FEBS Lett. 2001 Apr 6;494(1-2):44-7. doi: 10.1016/s0014-5793(01)02315-8.
The subcellular location of two integral membrane-bound fatty acid desaturases (Fads), Fad2 and Fad3, was elucidated by immunofluorescence microscopic analyses of tobacco suspension cells transiently transformed with different epitope-tagged versions of the enzymes. Both myc- or hemagglutinin-tagged Fad2 and Fad3 localized to the same region of the endoplasmic reticulum (ER), as evidenced by their co-localization with the ER lumenal protein calreticulin. Results from differential permeabilization experiments revealed that the N-termini of both epitope-tagged Fad2 and Fad3 were exposed on the cytosolic side of ER membranes. These data define the subcellular location and topological orientation of plant desaturases in ER membranes.
通过对用不同表位标签版本的酶瞬时转化的烟草悬浮细胞进行免疫荧光显微镜分析,阐明了两种整合膜结合脂肪酸去饱和酶(Fads)Fad2和Fad3的亚细胞定位。带有myc或血凝素标签的Fad2和Fad3都定位于内质网(ER)的同一区域,这通过它们与ER腔蛋白钙网蛋白的共定位得以证明。差异通透实验结果表明,带有表位标签的Fad2和Fad3的N末端都暴露在内质网膜的胞质侧。这些数据确定了植物去饱和酶在内质网膜中的亚细胞定位和拓扑方向。