Monroy A F, Gardiner W E, Schwartzbach S D
School of Biological Sciences, University of Nebraska, Lincoln 68588-0343.
Electrophoresis. 1988 Nov;9(11):764-73. doi: 10.1002/elps.1150091112.
Two-dimensional (2-D) gel electrophoresis has been used to follow changes in cell type specific and organelle localized polypeptides upon exposure of etiolated sorghum shoots and dark-grown resting Euglena to light. Total protein extracted from isolated bundle sheath strands and mesophyll protoplasts was resolved by 2-D gel electrophoresis. The cell type specific polypeptides were localized on the whole shoot 2-D gel map in order to determine changes in the levels of these polypeptides upon light exposure. An image analyzer was used to analyze fluorographs of 2-D gels of total Euglena protein pulse-labeled with [35S]sulfate in the dark, immediately upon light exposure and 1, 4, 14, 24, 48 and 72 h after light exposure. The subset of polypeptides whose relative rate of synthesis changes more than threefold immediately upon light exposure was identified. The different patterns of changes in the rate of synthesis of this subset of polypeptides were followed.
二维(2-D)凝胶电泳已被用于追踪黄化高粱幼苗和黑暗中生长的静止眼虫暴露于光照后,细胞类型特异性和细胞器定位多肽的变化。从分离的维管束鞘细胞束和叶肉原生质体中提取的总蛋白通过二维凝胶电泳进行分离。将细胞类型特异性多肽定位在整个幼苗的二维凝胶图谱上,以确定光照后这些多肽水平的变化。使用图像分析仪分析黑暗中用[35S]硫酸盐脉冲标记的眼虫总蛋白二维凝胶的荧光照片,在光照后立即以及光照后1、4、14、24、48和72小时进行分析。鉴定了光照后合成相对速率立即变化超过三倍的多肽子集。追踪了该多肽子集合成速率的不同变化模式。