作者: Daisuke Takahashi , Takashi Nagao , Shota Sotokawa , Kazunobu Toshima
DOI: 10.1039/C6MD00167J
关键词:
摘要: A purpose-designed anthraquinone–monoclonal antibody (anti-sialyl Lewis (sLea) mAb) hybrid 6 selectively bound to and effectively degraded the target glycoprotein, HSA (human serum albumin)–sLea conjugate 4. Degradation was achieved using long wavelength UV light irradiation in absence of any additives under neutral conditions. Furthermore, exhibited selective photo-cytotoxicity against sLea positive cancer cells A431 WiDr only upon photo-irradiation.