标题:Size-Dependent Facilitation of Cancer Cell Targeting by Proteins Adsorbed on Nanoparticles
作者:Su, Gaoxing; Zhou, Xiaofei; Zhou, Hongyu; Li, Ye; Zhang, Xianren; Liu, Yin; Cao, Dapeng; Yan, Bing
作者机构:[Su, Gaoxing; Zhou, Xiaofei; Liu, Yin] Shandong Univ, Sch Chem & Chem Engn, Jinan 250100, Peoples R China.; [Su, Gaoxing] Nantong Univ, Sch Pharm, K 更多
通讯作者:Zhou, Hongyu
通讯作者地址:[Zhou, HY; Yan, B]Jinan Univ, Guangzhou Key Lab Environm Exposure & Hlth, Sch Environm, Guangzhou 510632, Guangdong, Peoples R China;[Zhou, HY; Yan, B 更多
来源:ACS APPLIED MATERIALS & INTERFACES
出版年:2016
卷:8
期:44
页码:30037-30047
DOI:10.1021/acsami.6b10967
关键词:cell targeting; protein adsorption; nanomedicine; delivery; cell; recognition
摘要:Understandings of how biomolecules modify nanoparticles in a biological context and how these exchanges impact nano-biointeractions are fundamental to nanomedicine and nanotoxicology research. In. this work, cancer-targeting gold nanoparticles (TGNPs) with different sizes (5, 15, and 40 nm) were designed and synthesized. These nanoparticles spontaneously adsorbed proteins in complete cell culture medium (Dulbecco's modified Eagle's medium with 10% human serum). Although the:targeting ligands on the surface Of nanoparticles were likely to be shielded by adsorbed proteins, the targeting, capability of nanoparticles was maintained due to the highly dynamic nature of protein adsorption. By regulating the size and surface curvature of nanoparticles, we found that smaller TGNPs (5 nm, large surface curvature) recognize folate receptors on HeLa cells mainly through one-on-one bindings, and adsorbed proteins partially interfered with their binding, inducing a reduction of cell uptake by similar to 30%. Larger TGNPs (40 nm, small surface curvature) bound to cell surface receptors through multivalent interactions, and their binding affinity was, in contrast, enhanced by adsorbed proteins, resulting in an increased cell uptake by similar to 13%. Computational modeling further corroborated our experimental findings. The compelling findings from this work demonstrated how nanoparticle's size controlled its biological activity and provided key design principles for nanomedicine agents.
收录类别:EI;SCOPUS;SCIE
WOS核心被引频次:5
Scopus被引频次:5
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84994691357&doi=10.1021%2facsami.6b10967&partnerID=40&md5=42c9c134f6ef6b5c081d383f46b53b92
TOP