Lamvik M K, White L R, Eik-Nes K B
J Microsc. 1984 May;134(Pt 2):137-41. doi: 10.1111/j.1365-2818.1984.tb02502.x.
Tropomyosin Mg-paracrystals have been studied by positive and negative staining with uranyl acetate and sodium phosphotungstate, either unfixed or fixed with glutaraldehyde. Fixation causes changes in some of the paracrystal bands. Some of the bands are more intense when a positively-charged staining ion is used than when a negatively-charged ion is used, in both negative and positive-staining techniques. This result rules out the suggestion that negative staining is not affected by the charge of the stain in tropomyosin, and agrees with findings in other specimens. Therefore it is unlikely that any simple parameter based on residue size can be used to predict the image intensity from the amino acid sequence for tropomyosin. These staining patterns cast doubt on the earlier interpretation of a prominent white band in the paracrystal as an overlap of alpha-helical molecular ends.
利用醋酸铀和磷钨酸钠进行正染色和负染色,对原肌球蛋白镁副晶体进行了研究,样本既可以是未固定的,也可以是用戊二醛固定的。固定会导致副晶体的一些条带发生变化。在负染色和正染色技术中,当使用带正电荷的染色离子时,一些条带比使用带负电荷的离子时更明显。这一结果排除了关于负染色不受原肌球蛋白染色剂电荷影响的说法,并与其他样本的研究结果一致。因此,不太可能基于残基大小使用任何简单参数来从原肌球蛋白的氨基酸序列预测图像强度。这些染色模式对早期将副晶体中一条明显的白色条带解释为α-螺旋分子末端重叠的观点提出了质疑。