双杂交：一种体内蛋白质-蛋白质相互作用检测方法。 - Suppr | 超能文献

相似文献

1

The two-hybrid: an in vivo protein-protein interaction assay.双杂交：一种体内蛋白质-蛋白质相互作用检测方法。

Mol Biol Rep. 1995;21(2):119-27. doi: 10.1007/BF00986502.

2

Identification of proteins that interact with a protein of interest: applications of the yeast two-hybrid system.鉴定与目标蛋白相互作用的蛋白质：酵母双杂交系统的应用

Mol Cell Biochem. 1997 Jul;172(1-2):67-79.

3

Subunit interactions in the assembly of Saccharomyces cerevisiae DNA polymerase alpha.酿酒酵母DNA聚合酶α组装中的亚基相互作用。

Nucleic Acids Res. 2003 Apr 15;31(8):2056-65. doi: 10.1093/nar/gkg311.

4

Kcc4 associates with septin proteins of Saccharomyces cerevisiae.Kcc4与酿酒酵母的septin蛋白相关联。

FEBS Lett. 2001 Feb 2;489(2-3):197-201. doi: 10.1016/s0014-5793(01)02104-4.

5

Identifying Pex21p as a protein that specifically interacts with yeast seryl-tRNA synthetase.鉴定Pex21p为一种与酵母丝氨酸-tRNA合成酶特异性相互作用的蛋白质。

FEMS Microbiol Lett. 2002 Aug 27;214(1):101-6. doi: 10.1111/j.1574-6968.2002.tb11331.x.

6

A modified yeast three-hybrid system enabling both positive and negative selections.一种能够实现正选和负选的改良酵母三杂交系统。

Biotechnol Lett. 2018 Jul;40(7):1127-1134. doi: 10.1007/s10529-018-2567-7. Epub 2018 May 18.

7

A Comparison of Two-Hybrid Approaches for Detecting Protein-Protein Interactions.两种用于检测蛋白质-蛋白质相互作用的双杂交方法的比较

Methods Enzymol. 2017;586:333-358. doi: 10.1016/bs.mie.2016.10.020. Epub 2017 Jan 5.

8

Use of yeast two-hybrid system to evaluate Ras interactions with neurofibromin-GTPase-activating protein.利用酵母双杂交系统评估Ras与神经纤维瘤蛋白-鸟苷三磷酸酶激活蛋白的相互作用。

Methods Enzymol. 1995;255:488-97. doi: 10.1016/s0076-6879(95)55051-8.

9

Use of the two-hybrid system and random sonicated DNA to identify the interaction domain of a protein.利用双杂交系统和随机超声破碎的DNA来鉴定一种蛋白质的相互作用结构域。

Biotechniques. 1996 Sep;21(3):430-2. doi: 10.2144/96213bm20.

10

Structural and functional characterization of the amino terminal domain of the yeast ribosomal stalk P1 and P2 proteins.酵母核糖体柄部P1和P2蛋白氨基末端结构域的结构与功能表征

Int J Biochem Cell Biol. 2009 Jun;41(6):1315-22. doi: 10.1016/j.biocel.2008.11.005. Epub 2008 Nov 25.

引用本文的文献

1

Conserved interactions of the splicing factor Ntr1/Spp382 with proteins involved in DNA double-strand break repair and telomere metabolism.剪接因子Ntr1/Spp382与参与DNA双链断裂修复和端粒代谢的蛋白质之间的保守相互作用。

Nucleic Acids Res. 2007;35(7):2321-32. doi: 10.1093/nar/gkm127. Epub 2007 Mar 27.

2

Direct binding of a fragment of the Wiskott-Aldrich syndrome protein to the C-terminal end of the anaphylatoxin C5a receptor.威斯科特-奥尔德里奇综合征蛋白的一个片段与过敏毒素C5a受体C末端的直接结合。

Biochem J. 2003 Jun 1;372(Pt 2):453-63. doi: 10.1042/BJ20021803.

3

Identification and characterization of Prp45p and Prp46p, essential pre-mRNA splicing factors.

本文引用的文献

1

Strategies for the identification of interacting proteins.相互作用蛋白的鉴定策略。

Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):1639-41. doi: 10.1073/pnas.90.5.1639.

2

A genetic method for defining DNA-binding domains: application to the nuclear receptor NGFI-B.一种定义DNA结合结构域的遗传学方法：应用于核受体NGFI-B

Proc Natl Acad Sci U S A. 1993 Oct 1;90(19):9186-90. doi: 10.1073/pnas.90.19.9186.

3

Elimination of false positives that arise in using the two-hybrid system.消除在使用双杂交系统时出现的假阳性。