Stabilities of cubane type [Fe4S4(SR)4]2- clusters in partially aqueous media

被引:12
|
作者
Lo, Wayne [1 ]
Scott, Thomas A. [1 ]
Zhang, Ping [2 ]
Ling, Chang-Chun [2 ]
Holm, R. H. [1 ]
机构
[1] Harvard Univ, Dept Chem & Chem Biol, Cambridge, MA 02138 USA
[2] Univ Calgary, Dept Chem, Alberta Ingenu Ctr Carbohydrate Sci, Calgary, AB T2N 1N4, Canada
关键词
Iron-sulfur clusters; Cyclodextrin thiolates; Solution stability of clusters; IRON-SULFUR PROTEINS; SEQUENCE-SPECIFIC ASSIGNMENT; MAGNETIC CIRCULAR-DICHROISM; ACTIVE-SITES; SYNTHETIC ANALOGS; CRYSTAL-STRUCTURE; 4FE-4S CLUSTER; LIGAND; FERREDOXIN; CORE;
D O I
10.1016/j.jinorgbio.2010.12.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The stability of cubane-type [Fe4S4(SR)(4)](2-) clusters in mixed organic/aqueous solvents was examined as an initial step in the development of stable water-soluble cluster compounds possibly suitable for reconstitution of scaffold proteins in protein biosynthesis. The research involves primarily spectrophotometric assessment of stability in 20-80% Me2SO/aqueous media (v/v), from which it was found that conventional clusters tend to be stable for up to 12 h in 60% Me2SO but are much less stable at higher aqueous content. alpha-Cyclodextrin mono- and dithioesters and thiols were prepared as ligand precursors for cluster binding, which was demonstrated by spectroscopic methods. A potentially bidentate cyclodextrin dithiolate was found to be relatively effective for cluster stabilization in 40% Me2SO, suggesting (together with earlier results) that other exceptionally large thiolate ligands may promote cluster stability in aqueous media. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:497 / 508
页数:12
相关论文
共 50 条
  • [21] Ligand influence on the electronic structure and intrinsic redox properties of the [Fe4S4]2+ cubane clusters.
    Fu, YJ
    Yang, X
    Wang, XB
    Wang, LS
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2004, 227 : U1555 - U1555
  • [22] Terminal ligand influence on the electronic structure and intrinsic redox properties of the [Fe4S4]2+ cubane clusters
    Fu, YJ
    Yang, X
    Wang, XB
    Wang, LS
    INORGANIC CHEMISTRY, 2004, 43 (12) : 3647 - 3655
  • [23] 2-ELECTRON-TRANSFER OXIDATION BY POLYMER-SUPPORTED [FE4S4(SR)4]2- COMPLEX
    UEYAMA, N
    OKU, H
    NAKAMURA, A
    JOURNAL OF MOLECULAR CATALYSIS, 1992, 74 (1-3): : 451 - 458
  • [24] Terminal Ligand Assignments Based on Trends in Metal - Ligand Bond Lengths of Cubane-Type [Fe4S4]2+,+ Clusters
    Department of Chemistry, Harvard University, Cambridge, MA 02138, United States
    Inorg. Chem., 13 (3440-3443):
  • [25] Fe4S4 clusters as small molecule catalysts
    Noodleman, Louis
    NATURE CATALYSIS, 2018, 1 (06): : 383 - 384
  • [26] AN ELECTROCHEMICAL STUDY OF A SERIES OF [FE4S4(SR)4]2-COMPOUNDS
    OSULLIVAN, T
    MILLAR, M
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1984, 188 (AUG): : 157 - INOR
  • [27] Fe4S4 clusters as small molecule catalysts
    Louis Noodleman
    Nature Catalysis, 2018, 1 : 383 - 384
  • [28] [FE4S4(SH)4]2-, THE SIMPLEST SYNTHETIC ANALOG FOR A FERREDOXIN
    MULLER, A
    SCHLADERBECK, NH
    BOGGE, H
    JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1987, (01) : 35 - 36
  • [29] C-13 NUCLEAR-MAGNETIC-RESONANCE STUDIES OF SYNTHETIC [FE4S4(SR)4]2- IRON-SULFUR CLUSTERS
    OLLERENSHAW, TJ
    BRISTOW, S
    ANAND, BN
    GARNER, CD
    JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1986, (09): : 2013 - 2015
  • [30] [FE4S4(SR)4]-2- CATALYTIC REDUCTION OF DIPHENYLACETYLENE TO CIS-STILBENE IN THE PRESENCE OF NABH4
    ITOH, T
    NAGANO, T
    HIROBE, M
    TETRAHEDRON LETTERS, 1980, 21 (14) : 1343 - 1346