Ramshaw J A, Coyne J A, Lewontin R C
Genetics. 1979 Dec;93(4):1019-37. doi: 10.1093/genetics/93.4.1019.
Three experiments based on an idea of YOUDERIAN have been performed to determine the proportions and kinds of amino acid substitutions that are detected by gel electrophoresis when applied to surveys of protein variation in populations. The experiments involved applying the sequential method of electrophoresis under several conditions of pH and gel concentration to a large sample of human hemoglobins with known amino acid substitutions. In the first experiment, a random sample of 20 different hemoglobin variants was studied, and these were separated into 17 distinct electrophoretic classes by three sequential gel conditions, thus giving a detectability of 85%. A single pass under standard conditions detected eight classes. The second experiment compared groups of substitutions that were chemically identical, but in different positions in the alpha and beta chains, while the third experiment compared pairs of substitutions that were charge equivalent, but chemically different at the same chain position. The sequential method distinguished 90% of all chemically identical substitutions when they were at different chain locations, and four out of five charge equivalent but chemically different substitutions at the same site. Examination of the location of each substitution in the three-dimensional structure of hemoglobins showed that interior substitutions usually are less different from Hb A than are surface substitutions and that local interactions with chain and spatial neighbors are sufficient to distinguish substitutions in very similar positions on the outside of the molecule. The "charge ladder" model of electrophoretic classes is clearly incorrect, and it appears that sequential gel electrophoresis as practiced in our Drosophila surveys has detected a substantial fraction of amino acid substitutions if hemoglobin is regarded as a model. This estimate may be modified as other molecules beside hemoglobin are subjected to similar calibration experiments.
基于尤德里安的一个想法进行了三项实验,以确定在用于群体蛋白质变异调查时,通过凝胶电泳检测到的氨基酸取代的比例和种类。这些实验包括在几种pH值和凝胶浓度条件下,将连续电泳方法应用于大量已知氨基酸取代的人血红蛋白样本。在第一个实验中,研究了20种不同血红蛋白变体的随机样本,通过三种连续的凝胶条件将它们分离成17个不同的电泳类别,检测率为85%。在标准条件下单次电泳检测到8个类别。第二个实验比较了化学性质相同但在α链和β链不同位置的取代基团,而第三个实验比较了电荷等效但在同一链位置化学性质不同的取代基团对。当化学性质相同的取代基团位于不同链位置时,连续电泳方法能区分其中90%;在同一位置电荷等效但化学性质不同的取代基团中,能区分五分之四。对每种取代基团在血红蛋白三维结构中的位置进行检查表明,内部取代通常比表面取代与血红蛋白A的差异更小,并且与链和空间相邻基团的局部相互作用足以区分分子外部非常相似位置的取代基团。电泳类别的“电荷梯”模型显然是不正确的,并且如果将血红蛋白视为一个模型,那么在我们对果蝇的调查中所采用的连续凝胶电泳似乎已经检测到了相当一部分氨基酸取代。如果对除血红蛋白之外的其他分子进行类似的校准实验,这个估计可能会有所修改。