Thévenin Damien, An Ming, Engelman Donald M
Department of Molecular Biophysics and Biochemistry, Yale University, P.O. Box 208114, New Haven, CT 06520-8114, USA.
Chem Biol. 2009 Jul 31;16(7):754-62. doi: 10.1016/j.chembiol.2009.06.006.
Our goal is to define the properties of cell-impermeable cargo molecules that can be delivered into cells by pH (Low) Insertion Peptide (pHLIP), which can selectively target tumors in vivo based on their acidity. Using biophysical methods and fluorescence microscopy, we show that pHLIP can successfully deliver polar and membrane-impermeable cyclic peptides linked to its C terminus through the membranes of lipid vesicles and cancer cells. Our results also indicate that the translocation of these cargo molecules is pH dependent and mediated by transmembrane helix formation. Since a broad range of cell-impermeable molecules is excluded from discovery efforts because they cannot traverse membranes on their own, we believe that pHLIP has the potential to expand therapeutic options for acidic tissues such as tumors and sites of inflammation.
我们的目标是确定细胞不可渗透的货物分子的特性,这些分子可通过pH(低)插入肽(pHLIP)递送至细胞中,pHLIP能够基于肿瘤的酸度在体内选择性地靶向肿瘤。通过生物物理方法和荧光显微镜,我们表明pHLIP能够成功地将与其C末端相连的极性且膜不可渗透的环肽通过脂质囊泡和癌细胞的膜递送进去。我们的结果还表明,这些货物分子的转运是pH依赖性的,并且由跨膜螺旋的形成介导。由于广泛的细胞不可渗透分子因其自身无法穿过膜而被排除在发现工作之外,我们认为pHLIP有潜力扩大针对诸如肿瘤和炎症部位等酸性组织的治疗选择。