Comings D E
Clin Chem. 1982 Apr;28(4 Pt 2):782-9.
To understand at a molecular level the basis of the normal and pathological genetic differences between individuals it is necessary to begin a detailed two-dimensional gel electrophoretic mapping of the proteins of the human brain in normal individuals and those with various genetic neurological disorders. The present study is an examination of the polypeptide patterns of extracts of the human brain made with 9 mol/L urea solution. Details of the technique and the nomenclature of the patterns obtained are presented. the gels are separated into 20 sub-sections, based on standards with known molecular masses and isoelectric points. Groups of polypeptides within these sub-sections are identified by a number and a letter; the individual proteins are identified by a number. Thus, protein 1 in subsection 8, group b, would be designated 8b: 1. Subsequent papers in this series identify many of these proteins; show which proteins belong to the cytosol, synaptosome, myelin, and other brain fractions; show how these patterns vary between normal individuals and those with different neurological and psychiatric conditions; examine the effect of severe gliosis; and present the results of non-equilibrium gel electrophoresis for the more basic proteins.
为了在分子水平上理解个体之间正常和病理遗传差异的基础,有必要对正常个体以及患有各种遗传性神经疾病的个体的人脑蛋白质进行详细的二维凝胶电泳图谱分析。本研究是对用9摩尔/升尿素溶液制备的人脑提取物的多肽模式进行的检查。介绍了所采用技术的细节以及所获得模式的命名法。根据已知分子量和等电点的标准,将凝胶分为20个亚部分。这些亚部分内的多肽组由一个数字和一个字母标识;单个蛋白质由一个数字标识。因此,第8亚部分b组中的蛋白质1将被指定为8b:1。本系列的后续论文鉴定了其中许多蛋白质;展示了哪些蛋白质属于胞质溶胶、突触体、髓磷脂和其他脑部分;展示了这些模式在正常个体与患有不同神经和精神疾病的个体之间是如何变化的;研究了严重胶质增生的影响;并给出了针对碱性更强的蛋白质的非平衡凝胶电泳结果。