Dhuri Karishma, Duran Tibo, Chaudhuri Bodhisattwa, Slack Frank J, Vikram Ajit, Glazer Peter M, Bahal Raman
Department of Pharmaceutical Sciences, University of Connecticut, Storrs, CT 06269, USA.
Department of Chemical & Biomolecular Engineering, University of Connecticut, Storrs, CT 06269, USA.
Cell Rep Phys Sci. 2023 Oct 18;4(10). doi: 10.1016/j.xcrp.2023.101584. Epub 2023 Sep 15.
Gamma peptide nucleic acids (γPNAs) have recently garnered attention in diverse therapeutic and diagnostic applications. Serine and diethylene-glycol-containing γPNAs have been tested for numerous RNA-targeting purposes. Here, we comprehensively evaluated the and efficacy of pH-low insertion peptide (pHLIP)-conjugated serine and diethylene-based γPNAs. pHLIP targets only the acidic tumor microenvironment and not the normal cells. We synthesized and parallelly tested pHLIP-serine γPNAs and pHLIP-diethylene glycol γPNAs that target the seed region of microRNA-155, a microRNA that is upregulated in various cancers. We performed an all-atom molecular dynamics simulation-based computational study to elucidate the interaction of pHLIP-γPNA constructs with the lipid bilayer. We also determined the biodistribution and efficacy of the pHLIP constructs in the U2932-derived xenograft model. Overall, we established that the pHLIP-serine γPNAs show superior results compared with the pHLIP-diethylene glycol-based γPNA.
γ-肽核酸(γPNAs)最近在各种治疗和诊断应用中受到关注。含丝氨酸和二甘醇的γPNAs已针对多种RNA靶向目的进行了测试。在此,我们全面评估了pH低插入肽(pHLIP)偶联的丝氨酸和二甘醇基γPNAs的靶向和疗效。pHLIP仅靶向酸性肿瘤微环境,而非正常细胞。我们合成并平行测试了靶向微小RNA-155种子区域的pHLIP-丝氨酸γPNAs和pHLIP-二甘醇γPNAs,微小RNA-155在多种癌症中上调。我们进行了基于全原子分子动力学模拟的计算研究,以阐明pHLIP-γPNA构建体与脂质双层的相互作用。我们还确定了pHLIP构建体在U2932衍生的异种移植模型中的生物分布和疗效。总体而言我们确定,与基于pHLIP-二甘醇的γPNA相比,pHLIP-丝氨酸γPNAs显示出更好的结果。