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  • 教师姓名: 王斯佳
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  • 所在单位: 生命科学与技术学院
  • 学历: 博士研究生毕业
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  • 性别: 男
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  • 学位: 博士
  • 职称: 副教授
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Light-controlled delivery of monoclonal antibodies for targeted photoinactivation of Ki-67

发布时间:2025-04-30
点击次数:
发布时间:
2025-04-30
论文名称:
Light-controlled delivery of monoclonal antibodies for targeted photoinactivation of Ki-67
发表刊物:
Molecular Pharmaceutics
摘要:
The selective inhibition of intracellular and nuclear molecules such as Ki-67 holds great promise for the treatment of cancer and other diseases. However, the choice of the target protein and the intracellular delivery of the functional agent remain crucial challenges. Main hurdles are (a) an effective delivery into cells, (b)endosomal escape of the  delivered agents, and (c) an effective, externally triggered destruction of cells. Here we show a lightcontrolled two-step  approach for selective cellular delivery and cell elimination of proliferating cells. Three different cell-penetrating nano constructs, including liposomes, conjugates with the nuclear localization sequence (NLS), and conjugates with the cell penetrating peptide Pep-1, delivered the light activatable antibody conjugate TuBB-9-FITC, which targets the proliferation associated protein Ki-67. HeLa cells were treated with the photosensitizer benzoporphyrin monoacid derivative (BPD) and the antibody constructs. In the first optically controlled step, activation of BPD at 690 nm triggered a controlled endosomal escape of the TuBB-9-FITC constructs. In more than 75% of Ki-67 positive, irradiated cells TuBB-9-FITC antibodies relocated within 24 h from cytoplasmic organelles to the cell nucleus and bound to Ki-67. After a second light irradiation at 490 nm, which activated FITC, cell viability decreased to approximately 13%. Our study shows an effective targeting strategy, which uses light-controlled endosomal escape and the light inactivation of Ki-67 for cell elimination. The fact that liposomal or peptide-assisted delivery give similar results leads to the additional conclusion that an effective mechanism for endosomal escape leaves greater variability for the choice of the delivery agent.
合写作者:
Sijia Wang, Gereon Huttman, Zhenxi Zhang, Alfred Vogel,et al
卷号:
12(9)
页面范围:
3272-3281
是否译文:
发表时间:
2015-07-30