归巢(生物学)
肽
赫拉
共焦显微镜
化学
体外
生物物理学
流式细胞术
体内
药物输送
共焦
癌细胞
荧光寿命成像显微镜
细胞生物学
生物化学
生物
分子生物学
荧光
癌症
几何学
生态学
数学
遗传学
量子力学
有机化学
生物技术
物理
作者
Ruchika Goyal,Gaurav Jerath,R. Akhil,Aneesh Chandrasekharan,Eswara Rao Puppala,Srikanth Ponneganti,Anupam Sarma,V.G.M. Naidu,T.R. Santhoshkumar,Vibin Ramakrishnan
标识
DOI:10.1016/j.jconrel.2021.03.010
摘要
Poly-peptide molecules have shown promising applications in drug delivery and tumor targeting. A series of tumor homing peptides were designed by exhaustively sampling low energy geometrical basins of amino acids at specific sites of a peptide molecule to induce a conformational lock. This peptide library was pruned to a limited set of eight molecules, employing electrostatic interactions, docking, and molecular dynamics simulations. These designed and optimized peptides were synthesized and tested on various cell lines, including breast cancer (MDA-MB-231), cervical cancer (HeLa), osteosarcoma (U2-OS), and non-cancerous mammary epithelial cells (MCF-10A) using confocal microscopy and flow cytometry. Peptides show differential uptake in cancerous MDA-MB-231, HeLa, U2-OS, and non-cancerous MCF-10A cells. Confocal imaging verified their ability to penetrate even in 3D tumorospheres of MDA-MB-231 cells. Further, experiments of mitochondrial membrane potential depolarization and Caspase-3 activation confirmed that their cytotoxic effects are by apoptosis. Homing ability of the designed peptides in in vivo system and fluorescence imaging with clinical samples of human origin have further confirmed that the in vitro studies are qualitatively identical and quantitatively comparable in their ability to selectively recognize tumor cells. Overall, we present a roadmap for the functional programming of peptide-based homing and penetrating molecules that can perform selective tumor targeting.
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