Klose J, Willers I, Singh S, Goedde H W
Hum Genet. 1983;63(3):262-7. doi: 10.1007/BF00284661.
Proteins from cultured human fibroblasts and native human hair root cells were investigated using the two-dimensional electrophoresis (2DE) technique. Cell material from 35 different healthy persons was examined. Proteins of different sources were separated: total proteins of fibroblasts (12 cell lines), soluble proteins of fibroblasts (12 cell lines), structure-bound proteins of fibroblasts (eight cell lines) and soluble proteins of hair root cells (12 subjects). The protein samples of different individuals were run in pairs through the electrophoresis procedure and the two patterns of each pair were compared. All changes in the electrophoretic mobility of polypeptide spots (qualitative variants) and all clearly visible differences in the staining intensity of the spots (quantitative variants) were scored. Less than 1% of the qualitative variants per pattern was found in total cell proteins and this percentage was not increased in soluble proteins. No qualitative variation was detected in structure-bound proteins. Quantitative variation occurred to a considerably higher degree in the 2DE patterns than qualitative changes. The incidence of quantitative variants was about three times higher in soluble proteins (11%) than in structure-bound proteins (3.5%); in the total cell proteins it lay in between (7%). Cultured cells (fibroblasts) and native cells (hair root cells) showed a similar degree of variation. A comparison of the data shown here with data obtained by an investigation on inbred strains of the mouse suggest that the major part of the quantitative variants observed in the 2DE patterns of proteins were genetically determined. The results presented here and the mouse data mentioned above lead us to the conclusion that the genetic variability of proteins may be characterized by quantitative changes rather than by qualitative changes, and that the genetic variability occurs to quite different degrees in different classes of proteins: structure-bound proteins less than soluble non-enzymatic proteins less than enzymes (certain groups).
使用二维电泳(2DE)技术对培养的人成纤维细胞和天然人发根细胞中的蛋白质进行了研究。检测了来自35名不同健康个体的细胞材料。分离了不同来源的蛋白质:成纤维细胞的总蛋白(12个细胞系)、成纤维细胞的可溶性蛋白(12个细胞系)、成纤维细胞的结构结合蛋白(8个细胞系)和发根细胞的可溶性蛋白(12名受试者)。不同个体的蛋白质样品成对进行电泳,比较每对样品的两种图谱。对多肽斑点电泳迁移率的所有变化(定性变体)和斑点染色强度的所有明显差异(定量变体)进行评分。在总细胞蛋白中,每种图谱的定性变体不到1%,可溶性蛋白中的这一百分比没有增加。在结构结合蛋白中未检测到定性变化。二维电泳图谱中的定量变化比定性变化更为显著。可溶性蛋白(11%)中定量变体的发生率比结构结合蛋白(3.5%)高约三倍;在总细胞蛋白中,其发生率介于两者之间(7%)。培养细胞(成纤维细胞)和天然细胞(发根细胞)表现出相似的变异程度。将此处所示数据与对小鼠近交系进行调查获得的数据进行比较表明,在蛋白质二维电泳图谱中观察到的定量变体的主要部分是由基因决定的。此处给出的结果和上述小鼠数据使我们得出结论,蛋白质的遗传变异性可能以定量变化而非定性变化为特征,并且遗传变异性在不同类别的蛋白质中发生的程度差异很大:结构结合蛋白小于可溶性非酶蛋白小于酶(某些组)。