Development of an antibody-binding modular nanoplatform for antibody-guided targeted cell imaging and delivery

被引:22
|
作者
Kim, Hansol [1 ]
Kang, Young Ji [1 ]
Min, Junseon [1 ]
Choi, Hyeokjune [1 ]
Kang, Sebyung [1 ]
机构
[1] UNIST, Sch Life Sci, Dept Biol Sci, Ulsan, South Korea
来源
RSC ADVANCES | 2016年 / 6卷 / 23期
基金
新加坡国家研究基金会;
关键词
PROTEIN CAGE NANOPARTICLES; DRUG-DELIVERY; LUMAZINE SYNTHASE; CRYSTALLOGRAPHIC REFINEMENT; AQUIFEX-AEOLICUS; CANCER; IMMOBILIZATION; THERAPY; SURFACE; FUNCTIONALIZATION;
D O I
10.1039/c6ra00233a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A polyvalent antibody-binding lumazine synthase protein cage nanoparticle (ABD-AaLS) is constructed by genetically fusing lumazine synthase and antibody-binding domains. ABD-AaLS effectively captures targeting antibodies in an orientation-controlled manner by selectively binding to the Fc region of antibodies derived from a variety of species, such as rabbits, rats, and mice, on demand by simple molecular recognition. The resulting antibody/ABD-AaLS non-covalent complexes specifically recognize and bind to their target cells in vitro, guided by antibodies displayed on the surface of ABD-AaLS. ABD-AaLS has an additional internal cavity and exterior sites for encapsulation and attachment of cargo molecules such as drugs and diagnostic probes. ABD-AaLS effectively serves as a universal antibody-binding nanoplatform to display various targeting antibodies on demand through molecular recognition as well as to acquire additional functionalities without altering the essential properties of the targeting antibodies. ABD-AaLS may provide new opportunities to develop versatile target-dependent nanoscale theranostic systems.
引用
收藏
页码:19208 / 19213
页数:6
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