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用于热疗基因递送的智能生物合成纳米生物材料

Intelligent biosynthetic nanobiomaterials (IBNs) for hyperthermic gene delivery.

作者信息

Chen Tze-Haw Howard, Bae Younsoo, Furgeson Darin Y

机构信息

Division of Pharmaceutical Sciences, School of Pharmacy, University of Wisconsin-Madison, Madison, Wisconsin 53705-2222, USA.

出版信息

Pharm Res. 2008 Mar;25(3):683-91. doi: 10.1007/s11095-007-9382-5. Epub 2007 Aug 29.

Abstract

PURPOSE

Intelligent biosynthetic nanobiomaterials (IBNs) were constructed as recombinant diblock copolymers, notated as K8-ELP(1-60), containing a cationic oligolysine (VGK8G) and a thermosensitive elastin-like polypeptide (ELP) block with 60 repetitive pentapeptide units [(VPGXG)60; X is Val, Ala and Gly in a 5:2:3 ratio].

METHODS

K8-ELP(1-60) was synthesized by recursive directional ligation for DNA oligomerization. Purity and molecular weight of K8-ELP(1-60) were confirmed by SDS-PAGE and mass spectrometry. DNA polyplexes were prepared from K8-ELP(1-60) and pGL3-Control (pGL3-C) plasmid DNA (pDNA) and stability was evaluated by gel retardation, DLS, and DNA displacement with heparin. Thermal transition profiles were studied by measuring the turbidity change at 350 nm and the polyplexes were used to transfect MCF-7 cells with a concomitant cytotoxicity assay.

RESULTS

SDS-PAGE and MALDI-TOF studies showed highly pure copolymers at the desired molecular weight. K8-ELP(1-60) condensed pDNA at a cation to anion (N/P) ratio above 0.25 with a tight distribution of particle size ranging from 115.5-32.4 nm with increasing N/P ratio. Thermal transition temperatures of K8-ELP(1-60)/pDNA and K8-ELP(1-60) alone were 44.9 and 71.5 degrees C, respectively. K8-ELP(1-60)/pDNA complexes successfully transduced MCF-7 cells with qualitative expression of enhanced green fluorescent protein (EGFP) and minimal cytotoxicity compared to branched poly(ethyleneimine) controls.

CONCLUSIONS

K8-ELP(1-60) was successfully designed and purified through recombinant means with efficient and stable condensation of pDNA at N/P ratios>0.25 and polyplex particle size<115 nm. MCF-7 cells successfully expressed EGFP with minimal cytotoxicity compared to positive controls; moreover, polyplexes retained sharp, thermotransitive kinetics within a narrow Tt range at clinically relevant hyperthermic temperatures, where the decrease of Tt was due to the increased hydrophobicity upon charge neutralization.

摘要

目的

构建智能生物合成纳米生物材料(IBNs)作为重组二嵌段共聚物,记为K8-ELP(1-60),其包含一个阳离子寡聚赖氨酸(VGK8G)和一个具有60个重复五肽单元[(VPGXG)60;X为缬氨酸、丙氨酸和甘氨酸,比例为5:2:3]的热敏性弹性蛋白样多肽(ELP)嵌段。

方法

通过递归定向连接进行DNA寡聚化合成K8-ELP(1-60)。通过SDS-PAGE和质谱法确认K8-ELP(1-60)的纯度和分子量。由K8-ELP(1-60)和pGL3-Control(pGL3-C)质粒DNA(pDNA)制备DNA多聚体,并通过凝胶阻滞、动态光散射以及用肝素进行DNA置换来评估其稳定性。通过测量350nm处的浊度变化研究热转变曲线,并且使用多聚体转染MCF-7细胞并同时进行细胞毒性测定。

结果

SDS-PAGE和基质辅助激光解吸电离飞行时间研究表明,得到了具有所需分子量的高纯度共聚物。当阳离子与阴离子(N/P)比高于0.25时,K8-ELP(1-60)能凝聚pDNA,随着N/P比增加,粒径分布紧密,范围为115.5 - 32.4nm。K8-ELP(1-60)/pDNA和单独的K8-ELP(1-60)的热转变温度分别为44.9℃和71.5℃。与支链聚乙烯亚胺对照相比,K8-ELP(1-60)/pDNA复合物成功转导MCF-7细胞,增强型绿色荧光蛋白(EGFP)定性表达且细胞毒性最小。

结论

通过重组手段成功设计并纯化了K8-ELP(1-60),其在N/P比>0.25且多聚体粒径<115nm时能高效稳定地凝聚pDNA。与阳性对照相比,MCF-7细胞成功表达EGFP且细胞毒性最小;此外,在临床相关的热疗温度下窄的热转变温度范围内,多聚体保持了尖锐的热转变动力学,其中热转变温度的降低是由于电荷中和后疏水性增加所致。

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