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镧系元素配合物结构对细胞活力及结合的影响。

Effect of lanthanide complex structure on cell viability and association.

作者信息

Peterson Katie L, Dang Jonathan V, Weitz Evan A, Lewandowski Cutler, Pierre Valérie C

机构信息

Department of Chemistry, University of Minnesota , Minneapolis, Minnesota 55455, United States.

出版信息

Inorg Chem. 2014 Jun 16;53(12):6013-21. doi: 10.1021/ic500282n. Epub 2014 Jun 5.

Abstract

A systematic study of the effect of hydrophobicity and charge on the cell viability and cell association of lanthanide metal complexes is presented. The terbium luminescent probes feature a macrocyclic polyaminocarboxylate ligand (DOTA) in which the hydrophobicity of the antenna and that of the carboxyamide pendant arms are independently varied. Three sensitizing antennas were investigated in terms of their function in vitro: 2-methoxyisophthalamide (IAM(OMe)), 2-hydroxyisophthalamide (IAM), and 6-methylphenanthridine (Phen). Of these complexes, Tb-DOTA-IAM exhibited the highest quantum yield, although the higher cell viability and more facile synthesis of the structurally related Tb-DOTA-IAM(OMe) platform renders it more attractive. Further modification of this latter core structure with carboxyamide arms featuring hydrophobic benzyl, hexyl, and trifluoro groups as well as hydrophilic amino acid based moieties generated a family of complexes that exhibit high cell viability (ED50 > 300 μM) regardless of the lipophilicity or the overall complex charge. Only the hexyl-substituted complex reduced cell viability to 60% in the presence of 100 μM complex. Additionally, cellular association was investigated by ICP-MS and fluorescence microscopy. Surprisingly, the hydrophobic moieties did not increase cell association in comparison to the hydrophilic amino acid derivatives. It is thus postulated that the hydrophilic nature of the 2-methoxyisophthalamide antenna (IAM(OMe)) disfavors the cellular association of these complexes. As such, responsive luminescent probes based on this scaffold would be appropriate for the detection of extracellular species.

摘要

本文对疏水性和电荷对镧系金属配合物细胞活力和细胞结合的影响进行了系统研究。铽发光探针具有大环多氨基羧酸盐配体(DOTA),其中天线的疏水性和羧酰胺侧臂的疏水性可独立变化。研究了三种敏化天线在体外的功能:2-甲氧基间苯二甲酰胺(IAM(OMe))、2-羟基间苯二甲酰胺(IAM)和6-甲基菲啶(Phen)。在这些配合物中,Tb-DOTA-IAM表现出最高的量子产率,尽管结构相关的Tb-DOTA-IAM(OMe)平台具有更高的细胞活力和更简便的合成方法,使其更具吸引力。用具有疏水性苄基、己基和三氟基团以及亲水性氨基酸基部分的羧酰胺臂对后一种核心结构进行进一步修饰,产生了一系列配合物,无论其亲脂性或整体配合物电荷如何,都表现出高细胞活力(ED50>300μM)。只有己基取代的配合物在100μM配合物存在下将细胞活力降低到60%。此外,通过电感耦合等离子体质谱(ICP-MS)和荧光显微镜研究了细胞结合情况。令人惊讶的是,与亲水性氨基酸衍生物相比,疏水性部分并没有增加细胞结合。因此推测,2-甲氧基间苯二甲酰胺天线(IAM(OMe))的亲水性不利于这些配合物的细胞结合。因此,基于该支架的响应性发光探针适用于检测细胞外物质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5264/4060611/20cd48ebfafe/ic-2014-00282n_0001.jpg

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