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13种抗Sm单克隆抗体在6个不同亚组中免疫沉淀三种细胞质小核核糖核蛋白核心蛋白前体。

Thirteen anti-Sm monoclonal antibodies immunoprecipitate the three cytoplasmic snRNP core protein precursors in six distinct subsets.

作者信息

Fury M, Andersen J, Ponda P, Aimes R, Zieve G W

机构信息

Department of Pathology, SUNY Stony Brook, Stony Brook, NY 11794-8691, USA.

出版信息

J Autoimmun. 1999 Mar;12(2):91-100. doi: 10.1006/jaut.1998.0266.

DOI:10.1006/jaut.1998.0266
PMID:10047429
Abstract

The small nuclear ribonucleoprotein particle (snRNP) common core proteins are the lupus-associated Sm autoantigens. In mouse fibroblasts the seven snRNP core proteins form a particle with a suggested stoichiometry of B2[D1,D2(E,F,G)2] D3. Core particle assembly occurs in the cytoplasm where newly synthesized snRNAs assemble with core proteins stored in three RNA-free complexes of (1) a 6S complex of [D1,D2(E,F,G)2] (2) a 20S complex of (B,D3 and an unidentified 70 kDa protein) and (3) a 2S-6S complex that minimally contains the B protein. In this report a panel of 13 anti-Sm monoclonal antibodies is shown to immunoprecipitate six different subsets of the cytoplasmic snRNP proteins. Four epitopes are shared by the three aforementioned complexes and five other epitopes are shared by two of the complexes. In addition, the 6S or 20S complexes are apparently disrupted by five of the antibodies. Kinetic studies show that the three cytoplasmic snRNP protein complexes have independent half-lives. These studies provide another approach for characterizing the Sm epitopes. They also complement previous in vitro snRNP assembly studies and suggest that snRNP core assembly occurs by the initial binding of snRNA to the 6S particle followed by addition of the B and D3 proteins.

摘要

小核核糖核蛋白颗粒(snRNP)的共同核心蛋白是与狼疮相关的Sm自身抗原。在小鼠成纤维细胞中,七种snRNP核心蛋白形成一种颗粒,其化学计量比推测为B2[D1,D2(E,F,G)2] D3。核心颗粒组装发生在细胞质中,新合成的snRNAs与储存在三种无RNA复合物中的核心蛋白组装在一起,这三种复合物分别是:(1)[D1,D2(E,F,G)2]的6S复合物;(2)(B、D3和一种未鉴定的70 kDa蛋白)的20S复合物;(3)至少包含B蛋白的2S - 6S复合物。在本报告中,一组13种抗Sm单克隆抗体被证明能免疫沉淀细胞质snRNP蛋白的六个不同亚组。上述三种复合物共有四个表位,另外五个表位为其中两种复合物所共有。此外,6S或20S复合物显然被其中五种抗体破坏。动力学研究表明,三种细胞质snRNP蛋白复合物具有独立的半衰期。这些研究为表征Sm表位提供了另一种方法。它们还补充了先前的体外snRNP组装研究,并表明snRNP核心组装是通过snRNA首先与6S颗粒结合,随后添加B和D3蛋白而发生的。

相似文献

1
Thirteen anti-Sm monoclonal antibodies immunoprecipitate the three cytoplasmic snRNP core protein precursors in six distinct subsets.13种抗Sm单克隆抗体在6个不同亚组中免疫沉淀三种细胞质小核核糖核蛋白核心蛋白前体。
J Autoimmun. 1999 Mar;12(2):91-100. doi: 10.1006/jaut.1998.0266.
2
Multiple protein: protein interactions between the snRNP common core proteins.多种蛋白质:小核核糖核蛋白共同核心蛋白之间的蛋白质相互作用。
Exp Cell Res. 1997 Nov 25;237(1):63-9. doi: 10.1006/excr.1997.3750.
3
Monoclonal antibody specific to a subclass of polyproline-Arg motif provides evidence for the presence of an snRNA-free spliceosomal Sm protein complex in vivo: implications for molecular interactions involving proline-rich sequences of Sm B/B' proteins.针对多聚脯氨酸-精氨酸基序一个亚类的单克隆抗体为体内存在无小核RNA剪接体Sm蛋白复合物提供了证据:对涉及Sm B/B'蛋白富含脯氨酸序列的分子相互作用的影响。
J Cell Biochem. 1999 Aug 1;74(2):168-80.
4
The snRNP core assembly pathway: identification of stable core protein heteromeric complexes and an snRNP subcore particle in vitro.小核核糖核蛋白核心组装途径:体外稳定核心蛋白异源复合物和小核核糖核蛋白亚核心颗粒的鉴定。
EMBO J. 1996 May 1;15(9):2256-69.
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Human anti-nuclear ribonucleoprotein antigen autoimmune sera contain a novel subset of autoantibodies that stabilizes the molecular interaction of U1RNP-C protein with the Sm core proteins.人抗核糖核蛋白抗原自身免疫血清含有一类新型自身抗体,这类抗体可稳定U1RNP-C蛋白与Sm核心蛋白的分子相互作用。
J Immunol. 1997 May 15;158(10):5017-25.
6
Electron microscopy of assembly intermediates of the snRNP core: morphological similarities between the RNA-free (E.F.G) protein heteromer and the intact snRNP core.小核核糖核蛋白核心组装中间体的电子显微镜观察:无RNA的(E.F.G)蛋白质异源三聚体与完整小核核糖核蛋白核心之间的形态学相似性。
J Mol Biol. 1997 Jan 17;265(2):87-94. doi: 10.1006/jmbi.1996.0713.
7
The cytoplasmic sites of the snRNP protein complexes are punctate structures that are responsive to changes in metabolism and intracellular architecture.核内小核糖核蛋白(snRNP)蛋白质复合体的胞质位点是点状结构,对代谢和细胞内结构的变化有反应。
Exp Cell Res. 1999 Feb 25;247(1):249-56. doi: 10.1006/excr.1998.4354.
8
Mapping of SLE-specific Sm B cell epitopes using murine monoclonal antibodies.利用鼠单克隆抗体对系统性红斑狼疮特异性Sm B细胞表位进行定位
J Autoimmun. 1997 Apr;10(2):127-36. doi: 10.1006/jaut.1996.0123.
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Anti-Sm and anti-RNP antibodies.抗Sm抗体和抗RNP抗体。
Autoimmunity. 2005 Feb;38(1):47-54. doi: 10.1080/08916930400022715.
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Caspase-mediated cleavage of the U snRNP-associated Sm-F protein during apoptosis.细胞凋亡过程中Caspase介导的U小核核糖核蛋白相关Sm-F蛋白的裂解
Cell Death Differ. 2003 May;10(5):570-9. doi: 10.1038/sj.cdd.4401196.

引用本文的文献

1
The methylosome, a 20S complex containing JBP1 and pICln, produces dimethylarginine-modified Sm proteins.甲基化小体是一种含有JBP1和pICln的20S复合物,可产生二甲基精氨酸修饰的Sm蛋白。
Mol Cell Biol. 2001 Dec;21(24):8289-300. doi: 10.1128/MCB.21.24.8289-8300.2001.
2
Spliceosomal U snRNP core assembly: Sm proteins assemble onto an Sm site RNA nonanucleotide in a specific and thermodynamically stable manner.剪接体U snRNP核心组装:Sm蛋白以特定且热力学稳定的方式组装到Sm位点RNA九核苷酸上。
Mol Cell Biol. 1999 Oct;19(10):6554-65. doi: 10.1128/MCB.19.10.6554.