A photoswitchable CENP-E inhibitor with single blue-green light to control chromosome positioning in mitotic cells

被引:0
|
作者
Matsuo, Kazuya [1 ,2 ]
Kikukawa, Takashi [3 ]
Waku, Tomonori [2 ]
Kobori, Akio [2 ]
Tamaoki, Nobuyuki [1 ]
机构
[1] Hokkaido Univ, Res Inst Elect Sci, Kita 20,Nishi 10,Kita Ku, Sapporo, 0010020, Japan
[2] Kyoto Inst Technol, Fac Mol Chem & Engn, Sakyo Ku, Kyoto 6068585, Japan
[3] Hokkaido Univ, Fac Adv Life Sci, Kita 10,Nishi 8,Kita Ku, Sapporo, Hokkaido 0600810, Japan
来源
基金
日本学术振兴会;
关键词
AZOBENZENE PHOTOSWITCHES; AZO DYES; IN-VIVO;
D O I
10.1039/d4md00458b
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
Reversibly photoswitchable chemical tools have aided in the development of novel approaches in the biomedical field. The visible region of light should be ideal for the biological application of this approach because of its low phototoxicity and deep penetration depth compared to ultraviolet light. Herein, we report a photoswitchable centromere-associated protein E (CENP-E) inhibitor, which is controllable with low-energy blue-green light (around 500 nm) illumination. This photoswitchable tool enabled us to control CENP-E-driven chromosome movements and positioning at subcellular resolutions with low phototoxic effects. This study can contribute to the development of a unique technique for chromosome engineering. A photoswitchable centromere-associated protein E (CENP-E) inhibitor based on the 4-methylaminoazobenzene photoswitch is reported, which is characterized with cis-trans photoisomerization with blue-green light and fast thermal relaxation.
引用
收藏
页数:5
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    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2020, 142 (04) : 1763 - 1767
  • [2] CENP-E inhibitor potently activates cGAS-STING pathway through misaligned chromosome-mediated micronucleation after mitotic slippage
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    [J]. EUROPEAN JOURNAL OF CANCER, 2022, 174 : S47 - S48
  • [3] Defects in chromosome congression and mitotic progression in KIF18A-deficient cells are partly mediated through impaired functions of CENP-E
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    [J]. CELL CYCLE, 2009, 8 (16) : 2643 - 2649