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π 共轭荧光标记和酶响应的 l-氨基酸聚合物纳米载体及其在癌细胞中的可变色细胞内 FRET 探针。

π-Conjugate Fluorophore-Tagged and Enzyme-Responsive l-Amino Acid Polymer Nanocarrier and Their Color-Tunable Intracellular FRET Probe in Cancer Cells.

机构信息

Department of Chemistry, Indian Institute of Science Education and Research (IISER) Pune , Dr. Homi Bhabha Road, Pune 411008, Maharashtra, India.

出版信息

Biomacromolecules. 2017 Aug 14;18(8):2594-2609. doi: 10.1021/acs.biomac.7b00710. Epub 2017 Jul 24.

Abstract

The present investigation accounts one of the first example of enzyme-responsive and π-conjugate-tagged l-amino acid amphiphilic polymer and their fluorescence resonance energy transfer (FRET) probes for color-tunable intracellular bioimaging in cancer cells. Melt polymerizable oligo-phenylenevinylene (OPV) π-conjugated diol was tailor-made and subjected to thermo-selective melt transesterification reaction with multifunctional l-aspartic acid monomer to yield OPV-tagged amphiphilic luminescent polyesters. These amphiphilic polyesters self-assembled through strong aromatic π-π stacking and hydrophilic/hydrophobic noncovalent forces into <200 nm size blue-luminescent nanoparticles in aqueous medium. The OPV-tagged polymer nanoparticles served as FRET donor and encapsulated water insoluble Nile Red (NR) fluorophore as a FRET acceptor. Detail photophysical studies revealed that both the OPV and NR were confined within Förster distance in the polymer nanocontainer and the nanodomains provided appropriate geometry for efficient excitation energy transfer from OPV to NR. Cytotoxicity studies in breast cancer (MCF 7), cervical cancer (HeLa) and normal (Wild-type MEF) cell lines revealed that both the nascent luminescent OPV nanoparticles and OPV-NR FRET probes were nontoxic to cells up to 100 μg/mL. Confocal microscope images confirmed the efficient transportation of polymer and FRET probes across the cell membranes and their preferable accumulation in the cytoplasm of the cells. Lysosomal tracker assisted live cell imaging provided direct evidence for the localization of the polymer nanoparticles at the lysosomal compartments in the cytoplasm. In vitro enzyme-responsive studies revealed that the aliphatic polyester backbone in the polymer nanoparticles was readily biodegradable by lysosomal enzymes like esterase, chymotrypsin, trypsin, and also redox GSH species in the cytoplasm. Selective photoexcitation in confocal microscope exhibited bright OPV blue-luminescence and strong red-emission from NR followed by the excitation energy transfer and occurrence of FRET process at the intracellular environment in cancer cell lines. Both the polymer design and the biodegradable polymer FRET concept are completely new; thus, the present approach opens up new platform of research opportunities for natural l-amino acid based luminescent polymer probes for color-tunable bioimaging in cancer cells.

摘要

本研究报道了首例酶响应型和π共轭标记的 l-氨基酸两亲聚合物及其用于癌细胞中可调色彩的细胞内生物成像的荧光共振能量转移(FRET)探针之一。定制了可熔融聚合的寡苯乙烯(OPV)π共轭二醇,并与多功能 l-天冬氨酸单体进行热选择性熔融酯交换反应,得到 OPV 标记的两亲性发光聚酯。这些两亲性聚酯通过强芳香π-π堆积和亲水/疏水非共价相互作用自组装成水中尺寸小于 200nm 的蓝色发光纳米粒子。OPV 标记的聚合物纳米粒子作为 FRET 供体,并封装疏水性尼罗红(NR)荧光团作为 FRET 受体。详细的光物理研究表明,OPV 和 NR 都被限制在聚合物纳米容器内的Förster 距离内,纳米域提供了从 OPV 到 NR 的有效激发能量转移的适当几何形状。在乳腺癌(MCF 7)、宫颈癌(HeLa)和正常(野生型 MEF)细胞系中的细胞毒性研究表明,新生的发光 OPV 纳米粒子和 OPV-NR FRET 探针在高达 100μg/mL 的浓度下对细胞均无毒性。共焦显微镜图像证实了聚合物和 FRET 探针有效地穿过细胞膜运输,并在细胞质中优先积累。溶酶体示踪剂辅助活细胞成像提供了聚合物纳米粒子在细胞质溶酶体隔室中定位的直接证据。体外酶响应研究表明,聚合物纳米粒子中的脂肪族聚酯主链容易被溶酶体酶(如酯酶、糜蛋白酶、胰蛋白酶)以及细胞质中的氧化还原 GSH 物种降解。共焦显微镜中的选择性光激发显示出明亮的 OPV 蓝色发光和来自 NR 的强红色发射,随后在癌细胞系的细胞内环境中发生激发能量转移和 FRET 过程。聚合物设计和可生物降解聚合物 FRET 概念都是全新的;因此,本方法为基于天然 l-氨基酸的发光聚合物探针在癌细胞中的可调色彩生物成像开辟了新的研究机会平台。

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