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针对非组蛋白染色体高迁移率族蛋白1的单克隆抗体与高迁移率族蛋白1共同迁移至细胞核。

Monoclonal antibody against non-histone chromosomal protein high mobility group 1 Co-migrates with high mobility group 1 into the nucleus.

作者信息

Tsuneoka M, Imamoto N S, Uchida T

出版信息

J Biol Chem. 1986 Feb 5;261(4):1829-34.

PMID:3944111
Abstract

Non-histone chromosomal protein high mobility group 1 (HMG-1) rapidly migrates into the nucleus when injected into the cytoplasm of bovine fibroblasts and HeLa cells by red cell-mediated microinjection (Rechsteiner, M., and Kuehl, L. (1979) Cell 16, 901-908). We isolated hybridomas secreting monoclonal antibodies against HMG-1. One of these monoclonal antibodies, FR-1, inhibited in vitro binding of 125I-HMG-1 to chromatin isolated from FL cells. When 125I-HMG-1 was co-introduced with antibody FR-1 by red cell-mediated microinjection, antibody FR-1 did not prevent the accumulation of 125I-HMG-1 in the nucleus. When 125I-antibody FR-1 or fluorescein isothiocyanate antibody FR-1 was introduced into the cytoplasm of FL cells, most of the antibody did not accumulate in the nucleus. But when 125I- or fluorescein isothiocyanate antibody FR-1 was co-introduced with HMG-1 into the cytoplasm of FL cells, it did migrate into the nucleus.

摘要

非组蛋白染色体高迁移率族蛋白1(HMG-1)通过红细胞介导的显微注射注入牛成纤维细胞和HeLa细胞的细胞质后,会迅速迁移到细胞核中(雷施泰纳,M.,和库尔,L.(1979年)《细胞》16卷,901 - 908页)。我们分离出了分泌抗HMG-1单克隆抗体的杂交瘤。其中一种单克隆抗体FR-1抑制了125I-HMG-1与从FL细胞分离的染色质的体外结合。当通过红细胞介导的显微注射将125I-HMG-1与抗体FR-1共同引入时,抗体FR-1并未阻止125I-HMG-1在细胞核中的积累。当将125I-抗体FR-1或异硫氰酸荧光素抗体FR-1引入FL细胞的细胞质中时,大部分抗体并未在细胞核中积累。但是当将125I-或异硫氰酸荧光素抗体FR-1与HMG-1共同引入FL细胞的细胞质中时,它确实迁移到了细胞核中。

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