基于新型琼脂糖凝胶基质的乳糖阻遏蛋白-操纵基因复合物的稳定性 - Suppr

Stability of lac repressor-operator complexes in a new agarose-based gel matrix.

作者信息

Vossen K M, Fried M G

机构信息

Department of Biochemistry and Molecular Biology, Pennsylvania State University College of Medicine, Hershey 17033, USA.

出版信息

Nucleic Acids Res. 1995 Jun 25;23(12):2346-7. doi: 10.1093/nar/23.12.2346.

DOI:10.1093/nar/23.12.2346

PMID:7610068

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC307031/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09ae/307031/dc1d492b667c/nar00012-0276-a.jpg

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Stability of lac repressor-operator complexes in a new agarose-based gel matrix.基于新型琼脂糖凝胶基质的乳糖阻遏蛋白-操纵基因复合物的稳定性

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The resolution between two native proteins and between their sodium dodecyl sulfate-complexes in agarose and polyacrylamide gel electrophoresis.两种天然蛋白质之间以及它们在琼脂糖和聚丙烯酰胺凝胶电泳中的十二烷基硫酸钠复合物之间的分辨率。

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Equilibria and kinetics of lac repressor-operator interactions by polyacrylamide gel electrophoresis.通过聚丙烯酰胺凝胶电泳研究乳糖阻遏物-操纵基因相互作用的平衡与动力学

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SDS agarose gels for analysis of proteins.用于蛋白质分析的十二烷基硫酸钠琼脂糖凝胶

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Electrophoretic separation of biopolymers in a matrix of polyacrylamide covalently linked to agarose.在与琼脂糖共价连接的聚丙烯酰胺基质中对生物聚合物进行电泳分离。

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Detection of conformational and net charge differences in DNA-protein complexes by quantitative electrophoresis on polyacrylamide-agarose copolymer gels.

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Do DNA gel electrophoretic mobilities extrapolate to the free-solution mobility of DNA at zero gel concentration?DNA凝胶电泳迁移率能否外推至凝胶浓度为零时DNA在自由溶液中的迁移率？

Electrophoresis. 1998 May;19(5):635-42. doi: 10.1002/elps.1150190504.

Effect of DNA looping on the induction kinetics of the lac operon.DNA环化对乳糖操纵子诱导动力学的影响。

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TET repressor.tet operator complex formation induces conformational changes in the tet operator DNA.TET阻遏蛋白与tet操纵基因复合物的形成会诱导tet操纵基因DNA发生构象变化。

Nucleic Acids Res. 1984 Feb 24;12(4):2171-80. doi: 10.1093/nar/12.4.2171.

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Rapid agarose gel electrophoretic mobility shift assay for quantitating protein: RNA interactions.用于定量蛋白质：RNA相互作用的快速琼脂糖凝胶电泳迁移率变动分析

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Targeting of the UmuD, UmuD', and MucA' mutagenesis proteins to DNA by RecA protein.RecA蛋白将UmuD、UmuD'和MucA'诱变蛋白靶向至DNA。

Proc Natl Acad Sci U S A. 1993 Sep 1;90(17):8169-73. doi: 10.1073/pnas.90.17.8169.

Analysis of the thermodynamic linkage of DNA binding and ion binding for dimeric and tetrameric forms of the lac repressor.乳糖阻遏蛋白二聚体和四聚体形式的DNA结合与离子结合的热力学联系分析。

Eur J Biochem. 1994 Dec 15;226(3):869-76. doi: 10.1111/j.1432-1033.1994.00869.x.

Molecular sequestration stabilizes CAP-DNA complexes during polyacrylamide gel electrophoresis.分子隔离在聚丙烯酰胺凝胶电泳过程中稳定了CAP-DNA复合物。

Nucleic Acids Res. 1994 Nov 25;22(23):5054-9. doi: 10.1093/nar/22.23.5054.

Binding of the recA protein of Escherichia coli to single- and double-stranded DNA.大肠杆菌RecA蛋白与单链和双链DNA的结合。

J Biol Chem. 1981 Aug 25;256(16):8835-44.

The locus of sequence-directed and protein-induced DNA bending.序列导向和蛋白质诱导的DNA弯曲位点。

Nature. 1984;308(5959):509-13. doi: 10.1038/308509a0.

Kinetics and mechanism in the reaction of gene regulatory proteins with DNA.基因调控蛋白与DNA反应的动力学及机制

J Mol Biol. 1984 Jan 25;172(3):263-82. doi: 10.1016/s0022-2836(84)80026-1.

CAP and RNA polymerase interactions with the lac promoter: binding stoichiometry and long range effects.CAP与RNA聚合酶与乳糖操纵子启动子的相互作用：结合化学计量和远距离效应。

Nucleic Acids Res. 1983 Jan 11;11(1):141-58. doi: 10.1093/nar/11.1.141.

Equilibria and kinetics of lac repressor-operator interactions by polyacrylamide gel electrophoresis.通过聚丙烯酰胺凝胶电泳研究乳糖阻遏物-操纵基因相互作用的平衡与动力学

Nucleic Acids Res. 1981 Dec 11;9(23):6505-25. doi: 10.1093/nar/9.23.6505.

A gel electrophoresis method for quantifying the binding of proteins to specific DNA regions: application to components of the Escherichia coli lactose operon regulatory system.一种用于定量蛋白质与特定DNA区域结合的凝胶电泳方法：应用于大肠杆菌乳糖操纵子调控系统的组分

Nucleic Acids Res. 1981 Jul 10;9(13):3047-60. doi: 10.1093/nar/9.13.3047.

Comparison of nucleic acid-protein interactions in solution and in polyacrylamide gels.溶液中和聚丙烯酰胺凝胶中核酸与蛋白质相互作用的比较。

Anal Biochem. 1986 Feb 15;153(1):172-7. doi: 10.1016/0003-2697(86)90077-1.

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Stability of lac repressor-operator complexes in a new agarose-based gel matrix.

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