The Future of Bioorthogonal Chemistry

被引:387
作者
Devaraj, Neal K. [1 ]
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
DIELS-ALDER REACTION; SITU CLICK CHEMISTRY; IN-SITU; TETRAZINE CYCLOADDITIONS; STAUDINGER LIGATION; LIVING SYSTEMS; FATTY-ACIDS; CYCLOPROPENE; DRUG; RELEASE;
D O I
10.1021/acscentsci.8b00251
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Bioorthogonal reactions have found widespread use in applications ranging from glycan engineering to in vivo imaging. Researchers have devised numerous reactions that can be predictably performed in a biological setting. Depending on the requirements of the intended application, one or more reactions from the available toolkit can be readily deployed. As an increasing number of investigators explore and apply chemical reactions in living systems, it is clear that there are a myriad of ways in which the field may advance. This article presents an outlook on the future of bioorthogonal chemistry. I discuss currently emerging opportunities and speculate on how bioorthogonal reactions might be applied in research and translational settings. I also outline hurdles that must be cleared if progress toward these goals is to be made. Given the incredible past successes of bioorthogonal chemistry and the rapid pace of innovations in the field, the future is undoubtedly very bright.
引用
收藏
页码:952 / 959
页数:8
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共 71 条
  • [41] Presentation and detection of azide functionality in bacterial cell surface proteins
    Link, AJ
    Vink, MKS
    Tirrell, DA
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (34) : 10598 - 10602
  • [42] Live-Cell Protein Sulfonylation Based on Proximity-driven N-Sulfonyl Pyridone Chemistry
    Matsuo, Kazuya
    Nishikawa, Yuki
    Masuda, Marie
    Hamachi, Itaru
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2018, 57 (03) : 659 - 662
  • [43] Generation of a bacterium with a 21 amino acid genetic code
    Mehl, RA
    Anderson, JC
    Santoro, SW
    Wang, L
    Martin, AB
    King, DS
    Horn, DM
    Schultz, PG
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (04) : 935 - 939
  • [44] In situ click chemistry:: Enzyme-generated inhibitors of carbonic anhydrase II
    Mocharla, VP
    Colasson, B
    Lee, LV
    Röper, S
    Sharpless, KB
    Wong, CH
    Kolb, HC
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (01) : 116 - 120
  • [45] Murray CW, 2009, NAT CHEM, V1, P187, DOI [10.1038/NCHEM.217, 10.1038/nchem.217]
  • [46] Tetrazine-Responsive Self-immolative Linkers
    Neumann, Kevin
    Jain, Sarthak
    Gambardella, Alessia
    Walker, Sarah E.
    Valero, Elsa
    Lilienkampf, Annamaria
    Bradley, Mark
    [J]. CHEMBIOCHEM, 2017, 18 (01) : 91 - 95
  • [47] High-yielding Staudinger ligation of a phosphinothioester and azide to form a peptide
    Nilsson, BL
    Kiessling, LL
    Raines, RT
    [J]. ORGANIC LETTERS, 2001, 3 (01) : 9 - 12
  • [48] Rapid Ligations with Equimolar Reactants in Water with the Potassium Acyltrifluoroborate (KAT) Amide Formation
    Noda, Hidetoshi
    Eros, Gabor
    Bode, Jeffrey W.
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2014, 136 (15) : 5611 - 5614
  • [49] Rapid and Efficient Generation of Stable Antibody-Drug Conjugates via an Encoded Cyclopropene and an Inverse-Electron-Demand Diels-Alder Reaction
    Oller-Salvia, Benjami
    Kym, Gene
    Chin, Jason W.
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2018, 57 (11) : 2831 - 2834
  • [50] In Vivo Bioorthogonal Chemistry Enables Local Hydrogel and Systemic Pro-Drug To Treat Soft Tissue Sarcoma
    Oneto, Jose M. Mejia
    Khan, Irfan
    Seebald, Leah
    Royzen, Maksim
    [J]. ACS CENTRAL SCIENCE, 2016, 2 (07) : 476 - 482