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通过肽介导的相转移制备的用于高灵敏度蛋白酶传感和体内细胞凋亡成像的紧凑、可编程且稳定的生物功能化上转换纳米颗粒。

Compact, Programmable, and Stable Biofunctionalized Upconversion Nanoparticles Prepared through Peptide-Mediated Phase Transfer for High-Sensitive Protease Sensing and in Vivo Apoptosis Imaging.

作者信息

Zeng Tao, Zhang Tao, Wei Wei, Li Zhi, Wu Dan, Wang Li, Guo Jun, He Xuewen, Ma Nan

机构信息

†Key Laboratory of Health Chemistry and Molecular Diagnosis of Suzhou, College of Chemistry, Chemical Engineering and Materials Science, and ‡Testing and Analysis Center, Soochow University, Suzhou, Jiangsu 215123, People's Republic of China.

出版信息

ACS Appl Mater Interfaces. 2015 Jun 10;7(22):11849-56. doi: 10.1021/acsami.5b01446. Epub 2015 Jun 1.

Abstract

Protease represents an important class of biomarkers for disease diagnostics and drug screening. Conventional fluorescence-based probes for in vivo protease imaging suffer from short excitation wavelengths and poor photostability. Upconversion nanoparticles (UCNPs) hold great promise for biosensing and bioimaging because of their deep-tissue excitability, robust photostability, and minimal imaging background. However, producing highly stable and compact biofunctionalized UCNP probes with optimal bioresponsivity for in vivo imaging of protease activities still remains challenging and has not been previously demonstrated. Herein, we report facile preparation of highly compact and stable biofunctionalized UCNPs through peptide-mediated phase transfer for high-sensitive detection of protease in vitro and in vivo. We demonstrate that the polyhistidine-containing chimeric peptides could displace oleic acid molecules capped on UCNPs synthesized in organic solvents and, thereby, directly transfer UCNPs from the chloroform phase to the water phase. The resulting UCNPs possess high stability, programmable surface properties, and a compact coating layer with minimized thickness for efficient luminescence resonance energy transfer (LRET). On the basis of this strategy, we prepared LRET-based UCNP probes with optimal bioresponsivity for in vitro high-sensitive detection of trypsin and in vivo imaging of apoptosis for chemotherapy efficacy evaluation. The reported strategy could be extended to construct a variety of peptide-functionalized UCNPs for various biomedical applications.

摘要

蛋白酶是疾病诊断和药物筛选的一类重要生物标志物。传统的基于荧光的体内蛋白酶成像探针存在激发波长短和光稳定性差的问题。上转换纳米粒子(UCNPs)由于其深层组织激发性、强大的光稳定性和最小的成像背景,在生物传感和生物成像方面具有巨大潜力。然而,制备具有最佳生物反应性的高度稳定且紧凑的生物功能化UCNP探针用于蛋白酶活性的体内成像仍然具有挑战性,且此前尚未得到证实。在此,我们报告了通过肽介导的相转移简便制备高度紧凑且稳定的生物功能化UCNPs,用于体外和体内蛋白酶的高灵敏度检测。我们证明含多组氨酸的嵌合肽可以取代在有机溶剂中合成的UCNPs上封端的油酸分子,从而直接将UCNPs从氯仿相转移到水相。所得的UCNPs具有高稳定性、可编程的表面性质以及具有最小厚度的紧凑涂层,用于高效的发光共振能量转移(LRET)。基于此策略,我们制备了具有最佳生物反应性的基于LRET的UCNP探针,用于体外胰蛋白酶的高灵敏度检测以及体内凋亡成像以评估化疗疗效。所报道的策略可扩展用于构建多种用于各种生物医学应用的肽功能化UCNPs。

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