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利用免疫电子显微镜技术对染色质亚基结构中组蛋白H5进行定位。

Localization of histone H5 in the subunit organization of chromatin using immunoelectron microscopy.

作者信息

Mazen A, De Murcia G, Bernard S, Pouyet J, Champagne M

出版信息

Eur J Biochem. 1982 Sep;127(1):169-76. doi: 10.1111/j.1432-1033.1982.tb06852.x.

Abstract

In avian erythroid cells the erythrocyte-specific histone H5 is involved, like H1, in the packing of nucleosomes in the 25-nm chromatin fibers. In this study the distribution of histone H5 along the polynucleosomal chains was visualized by immunoelectron microscopy. Trinucleosomes from chicken erythrocytes and liver were used in order to test the specificity of the reaction with purified rabbit anti-H5 antibodies at various ionic strengths (5-80 mM). Long-chain chromatin was then reacted with anti-H5 antibodies and with sorted monomeric ferritin conjugate under chosen conditions. The antigenic determinants of histone H5 in the 25-nm fiber of long-chain chromatin (at 80 mM NaCl) are as accessible to the specific antibodies as in trinucleosomes. When the immunocomplexes were examined by electron microscopy in a low-ionic-strength buffer, permitting maximum extension of the chromatin structure on the grid, clusters of compacted nucleosomes were seen, separated by short regions of relaxed nucleosomes. Single nucleosomes enlarged by the antibodies are sometimes visible in the extended domains. We conclude that histone H5 is located primarily on series of adjacent nucleosomes but it can also be found on single nucleosomes located in the H1-enriched extended domains.

摘要

在鸟类红细胞中,红细胞特异性组蛋白H5与H1一样,参与25纳米染色质纤维中核小体的组装。在本研究中,通过免疫电子显微镜观察了组蛋白H5沿多核小体链的分布情况。使用来自鸡红细胞和肝脏的三核小体,以测试在不同离子强度(5 - 80 mM)下与纯化的兔抗H5抗体反应的特异性。然后在选定条件下,使长链染色质与抗H5抗体和分选的单体铁蛋白缀合物反应。长链染色质25纳米纤维中(在80 mM NaCl条件下)组蛋白H5的抗原决定簇与三核小体中的一样,能被特异性抗体识别。当在低离子强度缓冲液中通过电子显微镜检查免疫复合物时,在网格上染色质结构最大程度伸展的情况下,可以看到聚集的紧密核小体,它们被短的松弛核小体区域隔开。在伸展区域有时可见被抗体放大的单核小体。我们得出结论,组蛋白H5主要位于一系列相邻的核小体上,但也可以在富含H1的伸展区域中的单核小体上找到。

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