Jay F, Lambillotte M, Mühlethaler K
Eur J Cell Biol. 1983 Mar;30(1):1-8.
Rhodopseudomonas viridis thylakoid membrane polypeptides were characterised by SDS gels, 2 D gels and surface-specific iodination. Four polypeptides with apparent molecular weights of 38 000, 33 000, 27 000, and 24 000 (reaction centre) and three low molecular weight polypeptides 11 000, 8000 and 6000 (probably light harvesting polypeptides) were identified. Antibodies were produced against the polypeptides eluted from SDS gels and tested for specificity by an immunoblotting assay. The antibodies were bound to the membranes and viewed by electron microscopy using a modification of the ferritin labelling technique. It is suggested that antigenic determinants for the 38 000, 33 000, and 27 000 reaction centre polypeptides and the 11 000 and 8000 low molecular weight polypeptides are present on the cytoplasmic membrane surface. The 33 000, 27 000, 11 000 and 6000 polypeptides appear to have surface-located residues which can be iodinated. The photosynthetic membrane of Rps. viridis appears to be a highly asymmetrical membrane.
利用十二烷基硫酸钠凝胶、双向凝胶和表面特异性碘化法对绿硫红假单胞菌类囊体膜多肽进行了表征。鉴定出四种表观分子量分别为38000、33000、27000和24000(反应中心)的多肽,以及三种低分子量多肽11000、8000和6000(可能是捕光多肽)。制备了针对从十二烷基硫酸钠凝胶上洗脱下来的多肽的抗体,并通过免疫印迹分析检测其特异性。将抗体与膜结合,采用铁蛋白标记技术的改进方法通过电子显微镜观察。结果表明,38000、33000和27000反应中心多肽以及11000和8000低分子量多肽的抗原决定簇存在于细胞质膜表面。33000、27000、11000和6000多肽似乎具有可被碘化的位于表面的残基。绿硫红假单胞菌的光合膜似乎是一种高度不对称的膜。