Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan.
Institute of Low Temperature Science, Hokkaido University, Sapporo, 060-0819, Japan.
Angew Chem Int Ed Engl. 2020 Apr 6;59(15):6015-6020. doi: 10.1002/anie.201914826. Epub 2020 Feb 26.
Folate receptors (FRs) are membrane proteins involved in folic acid uptake, and the alpha isoform (FR-α) is overexpressed in ovarian and endometrial cancer cells. For fluorescence imaging of FRs in vivo, the near-infrared (NIR) region (650-900 nm), in which tissue penetration is high and autofluorescence is low, is optimal, but existing NIR fluorescent probes targeting FR-α show high non-specific tissue adsorption, and require prolonged washout to visualize tumors. We have designed and synthesized a new NIR fluorescent probe, FolateSiR-1, utilizing a Si-rhodamine fluorophore having a carboxy group at the benzene moiety, coupled to a folate ligand moiety through a negatively charged tripeptide linker. This probe exhibits very low background fluorescence and afforded a tumor-to-background ratio (TBR) of up to 83 in FR-expressing tumor-bearing mice within 30 min. Thus, FolateSiR-1 has the potential to contribute to the research in the field of biology and the clinical medicine.
叶酸受体(FRs)是参与叶酸摄取的膜蛋白,α 同工型(FR-α)在卵巢和子宫内膜癌细胞中过表达。为了在体内对 FRs 进行荧光成像,近红外(NIR)区域(650-900nm)是最佳选择,因为该区域组织穿透性高,自发荧光低,但现有的靶向 FR-α 的近红外荧光探针显示出高的非特异性组织吸附,并且需要长时间冲洗才能可视化肿瘤。我们设计并合成了一种新的近红外荧光探针 FolateSiR-1,利用具有羧基的硅罗丹明荧光团,通过带负电荷的三肽接头连接到叶酸配体部分。该探针显示出非常低的背景荧光,在 30 分钟内,在表达 FR 的荷瘤小鼠中,肿瘤与背景的比值(TBR)高达 83。因此,FolateSiR-1 有可能为生物学和临床医学领域的研究做出贡献。