Rational Design of Artificial Metalloenzymes: Case Studies in Myoglobin

被引:1
|
作者
Lin, Yingwu [1 ,2 ]
机构
[1] Univ South China, Sch Chem & Chem Engn, Hengyang 421001, Peoples R China
[2] Univ South China, Lab Prot Struct & Funct, Hengyang 421001, Peoples R China
基金
中国国家自然科学基金;
关键词
metalloprotein; metalloenzyme; heme protein; myoglobin; molecular design; NITRITE REDUCTASE-ACTIVITY; UNNATURAL AMINO-ACIDS; HEME-COPPER OXIDASE; DISULFIDE BOND; STRUCTURAL BASIS; CROSS-LINK; GENETIC INCORPORATION; DISTAL HISTIDINES; OXYGEN ACTIVATION; PROTEIN SCAFFOLD;
D O I
10.7536/PC180528
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Metalloenzymes play diverse important functions in biological systems. Meanwhile, design of artificial metalloenzymes may fine-tune and expand the functionalities of natural metalloenzymes, and even create novel enzymes with more advanced functions. Myoglobin (Mb) is an ideal protein model for design of heme proteins and other metalloenzymes. In recent years, various approaches have been developed for design of artificial metalloenzymes based on the protein scaffold of Mb, which include design of hydrogen-bonding network, intramolecular disulfide bond, the use of post-translational modifications, introduction of non-natural amino acids and non-native cofactors. This review summaries the recent progress in these aspects, which will help us understand the structure and function relationship of metalloenzymes, master the idea and methodologies of artificial metalloenzyme design, thereby promoting the rapid development in this field.
引用
收藏
页码:1464 / 1474
页数:11
相关论文
共 103 条
  • [51] Design of functional metalloproteins
    Lu, Yi
    Yeung, Natasha
    Sieracki, Nathan
    Marshall, Nicholas M.
    [J]. NATURE, 2009, 460 (7257) : 855 - 862
  • [52] Rationally tuning the reduction potential of a single cupredoxin beyond the natural range
    Marshall, Nicholas M.
    Garner, Dewain K.
    Wilson, Tiffany D.
    Gao, Yi-Gui
    Robinson, Howard
    Nilges, Mark J.
    Lu, Yi
    [J]. NATURE, 2009, 462 (7269) : 113 - U127
  • [53] Effect of Outer-Sphere Side Chain Substitutions on the Fate of the trans Iron-Nitrosyl Dimer in Heme/Nonheme Engineered Myoglobins (FeBMbs): Insights into the Mechanism of Denitrifying NO Reductases
    Matsumura, Hirotoshi
    Chakraborty, Saumen
    Reed, Julian
    Lu, Yi
    Moenne-Loccoz, Pierre
    [J]. BIOCHEMISTRY, 2016, 55 (14) : 2091 - 2099
  • [54] The Production of Nitrous Oxide by the Heme/Nonheme Diiron Center of Engineered Myoglobins (FeBMbs) Proceeds through a trans-Iron-Nitrosyl Dimer
    Matsumura, Hirotoshi
    Hayashi, Takahiro
    Chakraborty, Saumen
    Lu, Yi
    Moenne-Loccoz, Pierre
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2014, 136 (06) : 2420 - 2431
  • [55] A Designed Functional Metalloenzyme that Reduces O2 to H2O with Over One Thousand Turnovers
    Miner, Kyle D.
    Mukherjee, Arnab
    Gao, Yi-Gui
    Null, Eric L.
    Petrik, Igor D.
    Zhao, Xuan
    Yeung, Natasha
    Robinson, Howard
    Lu, Yi
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2012, 51 (23) : 5589 - 5592
  • [56] The Nature and Reactivity of Ferryl Heme in Compounds I and II
    Moody, Peter C. E.
    Raven, Emma L.
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 2018, 51 (02) : 427 - 435
  • [57] Intraprotein transmethylation via a CH3-Co(III) species in myoglobin reconstituted with a cobalt corrinoid complex
    Morita, Yoshitsugu
    Oohora, Koji
    Sawada, Akiyoshi
    Doitomi, Kazuki
    Ohbayashi, Jun
    Kamachi, Takashi
    Yoshizawa, Kazunari
    Hisaeda, Yoshio
    Hayashi, Takashi
    [J]. DALTON TRANSACTIONS, 2016, 45 (08) : 3277 - 3284
  • [58] Nanda V, 2010, NAT CHEM, V2, P15, DOI [10.1038/NCHEM.473, 10.1038/nchem.473]
  • [59] Design and engineering of artificial oxygen-activating metalloenzymes
    Nastri, Flavia
    Chino, Marco
    Maglio, Ornella
    Bhagi-Damodaran, Ambika
    Lu, Yi
    Lombardi, Angela
    [J]. CHEMICAL SOCIETY REVIEWS, 2016, 45 (18) : 5020 - 5054
  • [60] Manganese(V) Porphycene Complex Responsible for Inert C-H Bond Hydroxylation in a Myoglobin Matrix
    Ohora, Koji
    Meichin, Hiroyuki
    Kihira, Yushi
    Sugimoto, Hiroshi
    Shiro, Yoshitsugu
    Hayashi, Takashi
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2017, 139 (51) : 18460 - 18463