Marmaras V J, Tsakas S
Department of Biology, University of Patras, Greece.
Dev Biol. 1988 Oct;129(2):294-303. doi: 10.1016/0012-1606(88)90376-4.
Detailed analysis of haemocyte proteins by one-dimensional polyacrylamide gel electrophoresis during the late larval stages and white pupae of the Mediterranean fruit fly Ceratitis capitata reveals more than 50 polypeptides. A numbering system is established based on molecular weight on sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). Detailed examination leads to the conclusion that each protein resolved by our methods has its own characteristic kinetics of accumulation. The most abundant protein is unequivocally the 36-kDa band with an isoelectric point at 5.07, followed by the 47- and 54-kDa proteins. The 36-kDa band constitutes approximately 9% of total haemocyte protein. Comparison of the haemocyte protein pattern to that of cell-free haemolymph clearly shows that the protein bands at 81, 82, 85, and 87 kDa are common in both sources. We demonstrated by immunoblotting and pulse-labeled experiments followed by 2D SDS-PAGE that these protein bands which constitute the larval serum proteins were internalized into the haemocytes from the serum. By pulse labeling cells with [35S]methionine, separating polypeptides by one-dimensional PAGE electrophoresis, and comparing the rates of synthesis of over 50 individual polypeptides by fluorography, the following results were obtained: Three protein groups with distinct patterns of synthesis were noted: (1) proteins that are synthesized throughout the developmental period studied, (2) proteins whose synthesis begins at the wandering stage, and (3) proteins that are synthesized only during the feeding period. The 47-kDa protein shows the highest relative rate of synthesis, but since it is not the most accumulated band it must have a high turnover rate. Most of the labeled proteins were secreted into the incubation medium. The intracellular transit time was estimated to be about 11 min. Patterns of protein synthesis in haemocytes are regulated in a precise temporal sequence during the transformation of larvae to pupae. Their study yields a useful system for the analysis of molecular events in gene control.
通过一维聚丙烯酰胺凝胶电泳对地中海实蝇(Ceratitis capitata)幼虫后期和白色蛹期血细胞蛋白进行的详细分析,揭示了50多种多肽。基于十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)上的分子量建立了一个编号系统。详细检查得出结论,通过我们的方法分离出的每种蛋白质都有其独特的积累动力学特征。最丰富的蛋白质无疑是等电点为5.07的36 kDa条带,其次是47 kDa和54 kDa的蛋白质。36 kDa条带约占血细胞总蛋白的9%。将血细胞蛋白图谱与无细胞血淋巴的图谱进行比较,清楚地表明81 kDa、82 kDa、85 kDa和87 kDa的蛋白条带在两种来源中都很常见。我们通过免疫印迹和脉冲标记实验,随后进行二维SDS-PAGE证明,这些构成幼虫血清蛋白的蛋白条带从血清中内化到血细胞中。通过用[35S]甲硫氨酸脉冲标记细胞,通过一维PAGE电泳分离多肽,并通过荧光自显影比较50多种单个多肽的合成速率,得到了以下结果:注意到有三组蛋白质具有不同的合成模式:(1)在整个研究的发育时期都合成的蛋白质,(2)在漫游阶段开始合成的蛋白质,(3)仅在取食期合成的蛋白质。47 kDa的蛋白质显示出最高的相对合成速率,但由于它不是积累最多的条带,它一定有很高的周转率。大多数标记蛋白被分泌到孵育培养基中。细胞内转运时间估计约为11分钟。在幼虫向蛹的转变过程中,血细胞中的蛋白质合成模式按照精确的时间顺序受到调节。它们的研究为分析基因控制中的分子事件提供了一个有用的系统。