Department of Bioscience and Biotechnology, Konkuk University, Seoul 05029, Republic of Korea.
J Microbiol Biotechnol. 2022 Sep 28;32(9):1209-1216. doi: 10.4014/jmb.2207.07058. Epub 2022 Aug 29.
To better understand the effects of PEGylation and biotinylation on the delivery efficiency of proteins, the cationic protein lysozyme (LZ) and anionic protein bovine serum albumin (BSA) were chemically conjugated with poly(ethylene glycol) (PEG) and biotin-PEG to primary amine groups of proteins using N-hydroxysuccinimide reactions. Four types of protein conjugates were successfully prepared: PEGylated LZ (PEG-LZ), PEGylated BSA (PEG-BSA), biotin-PEG-conjugated LZ (Bio-PEG-LZ), and biotin-PEG-conjugated BSA (Bio-PEG-BSA). PEG-LZ and Bio-PEG-LZ exhibited a lower intracellular uptake than that of LZ in A549 human lung cancer cells (in a two-dimensional culture). However, Bio-PEG-BSA showed significantly improved intracellular delivery as compared to that of PEG-BSA and BSA, probably because of favorable interactions with cells via biotin receptors. For A549/fibroblast coculture spheroids, PEG-LZ and PEG-BSA exhibited significantly decreased tissue penetration as compared with that of unmodified proteins. However, Bio-PEG-BSA showed tissue penetration comparable to that of unmodified BSA. In addition, citraconlyated LZ (Cit-LZ) showed reduced spheroid penetration as compared to that of LZ, probably owing to a decrease in protein charge. Taken together, chemical conjugation of targeting ligands-PEG to anionic proteins could be a promising strategy to improve intracellular delivery and in vivo activity, whereas modifications of cationic proteins should be more delicately designed.
为了更好地理解聚乙二醇(PEG)化和生物素化对蛋白质递药效率的影响,使用 N-羟基琥珀酰亚胺反应,将阳离子蛋白溶菌酶(LZ)和阴离子蛋白牛血清白蛋白(BSA)化学偶联到蛋白质的伯胺基团上,得到聚乙二醇(PEG)和生物素-PEG。成功制备了四种蛋白质缀合物:PEG 化 LZ(PEG-LZ)、PEG 化 BSA(PEG-BSA)、生物素-PEG 偶联 LZ(Bio-PEG-LZ)和生物素-PEG 偶联 BSA(Bio-PEG-BSA)。与 LZ 相比,在 A549 人肺癌细胞(二维培养)中,PEG-LZ 和 Bio-PEG-LZ 的细胞内摄取率较低。然而,与 PEG-BSA 和 BSA 相比,Bio-PEG-BSA 显示出明显改善的细胞内递药作用,这可能是由于其通过生物素受体与细胞发生有利相互作用所致。对于 A549/成纤维细胞共培养球体,与未修饰的蛋白质相比,PEG-LZ 和 PEG-BSA 的组织穿透性显著降低。然而,Bio-PEG-BSA 显示出与未修饰的 BSA 相当的组织穿透性。此外,与 LZ 相比,柠康酰化 LZ(Cit-LZ)的球体穿透性降低,这可能是由于蛋白质电荷减少所致。总之,将靶向配体-PEG 化学偶联到阴离子蛋白上可能是提高细胞内递药效率和体内活性的一种很有前途的策略,而阳离子蛋白的修饰应更精心设计。