Structural Biology and Nanomedicine Laboratory, Department of Biotechnology and Medical Engineering, National Institute of Technology , Rourkela 769008, Odisha, India.
ACS Appl Mater Interfaces. 2015 Dec 30;7(51):28177-87. doi: 10.1021/acsami.5b06076. Epub 2015 Dec 18.
Self-assembly of a protein is a natural phenomenon; however, the process can be performed under a suitable condition in vitro. Since proteins are nontoxic, biodegradable, and biocompatible in nature, they are used in various industrial applications such as biocatalyst, therapeutic agent, and drug carriers. Moreover, their flexible structural state and specific activity are being used as sensors and immensely attract many new applications. However, the inherent potential of protein self-assembly for various applications is yet to be explored in detail. In this study, spherical self-assembly of bovine α-lactalbumin (nsBLA) was synthesized using an optimized ethanol-mediated desolvation process with an average diameter of approximately 300 nm. The self-assembly was found to be highly stable against thermal, pH, and proteases stress. When nsBLA was administered in various cancer cells, it demonstrated high cytotoxicity in three different cancer cells via reactive oxygen species (ROS) generation, whereas it exhibited negligible toxicity in normal human and murine cells. When nsBLA was conjugated with folic acid, it improved the cytotoxicity and perhaps mediated through enhanced cellular uptake in cancer cells through binding with folate receptors. Further, experimental results confirmed that the cancer cell death induced by nsBLA was not caused by apoptosis but a necrotic-like death mechanism. When compared with a well-known protein-based anticancer agent BAMLET (bovine α-lactalbumin made lethal against tumor cell), the self-assembled BLA clearly exhibited higher cytotoxicity to cancer cells than BAMLET. While BAMLET exhibits poor biocompatibility, our nsBLA demonstrated excellent biocompatibility to normal cells. Therefore, in this study, we prepared self-assembled α-lactalbumin that exhibits strong inherent antiproliferative potential in multiple cancer cells which can be used for efficient therapeutic approach in cancer.
蛋白质的自组装是一种自然现象;然而,该过程可以在合适的条件下在体外进行。由于蛋白质在性质上是非毒性、可生物降解和生物相容的,因此它们被用于各种工业应用,如生物催化剂、治疗剂和药物载体。此外,它们灵活的结构状态和特定的活性被用作传感器,并吸引了许多新的应用。然而,蛋白质自组装在各种应用中的固有潜力尚未被详细探索。在这项研究中,使用优化的乙醇介导去溶剂化过程合成了具有约 300nm 平均直径的牛α-乳白蛋白(nsBLA)的球形自组装体。发现自组装体对热、pH 和蛋白酶胁迫具有高度稳定性。当 nsBLA 施用于各种癌细胞时,它通过生成活性氧(ROS)在三种不同的癌细胞中表现出高细胞毒性,而在正常人和鼠细胞中表现出可忽略的毒性。当 nsBLA 与叶酸结合时,它通过与叶酸受体结合,提高了癌细胞中的细胞摄取,从而提高了细胞毒性,这可能是通过增强细胞摄取来介导的。此外,实验结果证实,nsBLA 诱导的癌细胞死亡不是由细胞凋亡引起的,而是由坏死样死亡机制引起的。与一种著名的基于蛋白质的抗癌剂 BAMLET(牛α-乳白蛋白使肿瘤细胞致死)相比,自组装的 BLA 对癌细胞的细胞毒性明显高于 BAMLET。虽然 BAMLET 表现出较差的生物相容性,但我们的 nsBLA 对正常细胞表现出优异的生物相容性。因此,在这项研究中,我们制备了自组装的α-乳白蛋白,它在多种癌细胞中表现出强烈的内在抗增殖潜力,可以用于癌症的有效治疗方法。