Suppr超能文献

利用多重标记对蛋白质局部构象变化进行高分辨率探测:通过自旋、荧光和化学反应性探针监测人碳酸酐酶II的去折叠和自组装。

High-resolution probing of local conformational changes in proteins by the use of multiple labeling: unfolding and self-assembly of human carbonic anhydrase II monitored by spin, fluorescent, and chemical reactivity probes.

作者信息

Hammarström P, Owenius R, Mårtensson L G, Carlsson U, Lindgren M

机构信息

Department of Chemistry, Linköping University, SE-581 83 Linköping, Sweden.

出版信息

Biophys J. 2001 Jun;80(6):2867-85. doi: 10.1016/S0006-3495(01)76253-4.

Abstract

Two different spin labels, N-(1-oxyl-2,2,5,5-tetramethyl-3-pyrrolidinyl)iodoacetamide (IPSL) and (1-oxyl-2,2,5,5-tetramethylpyrroline-3-methyl) methanethiosulfonate (MTSSL), and two different fluorescent labels 5-((((2-iodoacetyl)amino)-ethyl)amino)naphtalene-1-sulfonic acid (IAEDANS) and 6-bromoacetyl-2-dimetylaminonaphtalene (BADAN), were attached to the introduced C79 in human carbonic anhydrase (HCA II) to probe local structural changes upon unfolding and aggregation. HCA II unfolds in a multi-step manner with an intermediate state populated between the native and unfolded states. The spin label IPSL and the fluorescent label IAEDANS reported on a substantial change in mobility and polarity at both unfolding transitions at a distance of 7.4-11.2 A from the backbone of position 79. The shorter and less flexible labels BADAN and MTSSL revealed less pronounced spectroscopic changes in the native-to-intermediate transition, 6.6-9.0 A from the backbone. At intermediate guanidine (Gu)-HCl concentrations the occurrence of soluble but irreversibly aggregated oligomeric protein was identified from refolding experiments. At approximately 1 M Gu-HCl the aggregation was found to be essentially complete. The size and structure of the aggregates could be varied by changing the protein concentration. EPR measurements and line-shape simulations together with fluorescence lifetime and anisotropy measurements provided a picture of the self-assembled protein as a disordered protein structure with a representation of both compact as well as dynamic and polar environments at the site of the molecular labels. This suggests that a partially folded intermediate of HCA II self-assembles by both local unfolding and intermolecular docking of the intermediates vicinal to position 79. The aggregates were determined to be 40-90 A in diameter depending on the experimental conditions and spectroscopic technique used.

摘要

将两种不同的自旋标记物N-(1-氧基-2,2,5,5-四甲基-3-吡咯烷基)碘乙酰胺(IPSL)和(1-氧基-2,2,5,5-四甲基吡咯啉-3-甲基)甲硫基磺酸盐(MTSSL),以及两种不同的荧光标记物5-((((2-碘乙酰基)氨基)-乙基)氨基)萘-1-磺酸(IAEDANS)和6-溴乙酰基-2-二甲基氨基萘(BADAN),连接到人碳酸酐酶(HCA II)中引入的C79上,以探测其在去折叠和聚集过程中的局部结构变化。HCA II以多步方式去折叠,在天然态和去折叠态之间存在一个中间态。自旋标记物IPSL和荧光标记物IAEDANS在距离79位主链7.4-11.2 Å处的两个去折叠转变中均报告了迁移率和极性的显著变化。较短且柔韧性较差的标记物BADAN和MTSSL在天然态到中间态的转变中(距离主链6.6-9.0 Å)显示出不太明显的光谱变化。在中间胍(Gu)-HCl浓度下,从复性实验中鉴定出可溶性但不可逆聚集的寡聚蛋白的存在。在约1 M Gu-HCl时,发现聚集基本完成。聚集物的大小和结构可通过改变蛋白质浓度而变化。电子顺磁共振(EPR)测量和线形模拟以及荧光寿命和各向异性测量提供了一幅自组装蛋白质的图像,其为一种无序的蛋白质结构,在分子标记位点既有紧密的环境,也有动态和极性的环境。这表明HCA II的部分折叠中间态通过79位附近中间态的局部去折叠和分子间对接进行自组装。根据实验条件和所使用的光谱技术,确定聚集物的直径为40-90 Å。

相似文献

2
Properties of spin and fluorescent labels at a receptor-ligand interface.
Biophys J. 1999 Oct;77(4):2237-50. doi: 10.1016/S0006-3495(99)77064-5.

引用本文的文献

2
Photophysical Properties of BADAN Revealed in the Study of GGBP Structural Transitions.
Int J Mol Sci. 2021 Oct 15;22(20):11113. doi: 10.3390/ijms222011113.
3
Exploring the structure of the 100 amino-acid residue long N-terminus of the plant antenna protein CP29.
Biophys J. 2014 Mar 18;106(6):1349-58. doi: 10.1016/j.bpj.2013.11.4506.
4
Transient conformational remodeling of folding proteins by GroES-individually and in concert with GroEL.
J Chem Biol. 2013 Oct 5;7(1):1-15. doi: 10.1007/s12154-013-0106-5. eCollection 2013.
5
Conformational dynamics of titin PEVK explored with FRET spectroscopy.
Biophys J. 2012 Oct 3;103(7):1480-9. doi: 10.1016/j.bpj.2012.08.042. Epub 2012 Oct 2.
6
Structural interactions between lipids, water and S1-S4 voltage-sensing domains.
J Mol Biol. 2012 Nov 2;423(4):632-47. doi: 10.1016/j.jmb.2012.07.015. Epub 2012 Jul 31.
9
Site-directed fluorescence labeling of a membrane protein with BADAN: probing protein topology and local environment.
Biophys J. 2008 May 15;94(10):3945-55. doi: 10.1529/biophysj.107.125807. Epub 2008 Jan 30.
10
Use of electron paramagnetic resonance spectroscopy to evaluate the redox state in vivo.
Antioxid Redox Signal. 2007 Oct;9(10):1757-71. doi: 10.1089/ars.2007.1718.

本文引用的文献

1
AMINO ACID COMPOSITION OF VARIOUS FORMS OF BOVINE AND HUMAN ERYTHROCYTE CARBONIC ANHYDRASE.
Biochim Biophys Acta. 1964 Apr 6;85:141-51. doi: 10.1016/0926-6569(64)90174-9.
3
Structural mapping of an aggregation nucleation site in a molten globule intermediate.
J Biol Chem. 1999 Nov 12;274(46):32897-903. doi: 10.1074/jbc.274.46.32897.
4
Properties of spin and fluorescent labels at a receptor-ligand interface.
Biophys J. 1999 Oct;77(4):2237-50. doi: 10.1016/S0006-3495(99)77064-5.
5
Recent advances in site-directed spin labeling of proteins.
Curr Opin Struct Biol. 1998 Oct;8(5):649-56. doi: 10.1016/s0959-440x(98)80158-9.
6
Diffusible, nonfibrillar ligands derived from Abeta1-42 are potent central nervous system neurotoxins.
Proc Natl Acad Sci U S A. 1998 May 26;95(11):6448-53. doi: 10.1073/pnas.95.11.6448.
9

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验