Harnessing sortase A transpeptidation for advanced targeted therapeutics and vaccine engineering

被引:8
|
作者
Obeng, Eugene M. [1 ]
Fulcher, Alex J. [2 ]
Wagstaff, Kylie M. [1 ]
机构
[1] Monash Univ, Biomed Discovery Inst, Dept Biochem & Mol Biol, Clayton, Vic 3800, Australia
[2] Monash Univ, Monash Micro Imaging, Clayton, Vic 3800, Australia
关键词
Sortase-mediated ligation; targeted delivery systems; multivalent therapeutics; adoptive cellular therapies; vaccine engineering; avidity-inspired technologies; STAPHYLOCOCCUS-AUREUS SORTASE; SITE-SPECIFIC MODIFICATION; SURFACE-PROTEINS; DRUG-DELIVERY; CELL-WALL; ANTIMICROBIAL RESISTANCE; SUBSTRATE-SPECIFICITY; MEDIATED LIGATIONS; CO-DELIVERY; PEPTIDE;
D O I
10.1016/j.biotechadv.2023.108108
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The engineering of potent prophylactic and therapeutic complexes has always required careful protein modifi-cation techniques with seamless capabilities. In this light, methods that favor unobstructed multivalent targeting and correct antigen presentations remain essential and very demanding. Sortase A (SrtA) transpeptidation has exhibited these attributes in various settings over the years. However, its applications for engineering avidity-inspired therapeutics and potent vaccines have yet to be significantly noticed, especially in this era where active targeting and multivalent nanomedications are in great demand. This review briefly presents the SrtA enzyme and its associated transpeptidation activity and describes interesting sortase-mediated protein engi-neering and chemistry approaches for achieving multivalent therapeutic and antigenic responses. The review further highlights advanced applications in targeted delivery systems, multivalent therapeutics, adoptive cellular therapy, and vaccine engineering. These innovations show the potential of sortase-mediated techniques in facilitating the development of simple plug-and-play nanomedicine technologies against recalcitrant diseases and pandemics such as cancer and viral infections.
引用
收藏
页数:18
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