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Development of a fluid functionalized lipidic matrix applied to direct in situ polynucleotide detection

机译:用于直接原位多核苷酸检测的流体功能化脂质基质的开发

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This work presents a new approach for direct detection of polyelectrolytes at the air-water interface, based on the investigation of the interfacial properties of an active lipidic matrix especially designed for polynucleotide immobilization. A synthetic lipid with a cationic spermine headgroup, DiOctadecylamidoGlycylSpermine (DOGS), was spread at the interface to form a distortable film able to capture polynucleotides. The control of the organization state of this functionalized monolayer upon compression was achieved by recording surface pressure-area (pi-A) isotherm diagrams, presenting a specific shape with a typical liquid expanded-liquid condensed phase transition on a pure water subphase. In the presence of various dsDNA concentrations in the subphase, the isotherms were markedly modified in a time and concentration-dependent manner. The main modifications, corresponding to a large shift towards higher molecular areas and a clear fading of the phase transition, were corroborated by the fine analysis of the monolayer compressibility profile, thus suggesting a characteristic change in the monolayer fluidity as a function of both time and DNA concentration. Moreover, an ATR-Fourier transform infrared (ATR-FTIR) characterization showed evidences for the adsorption of DNA strands onto the lipidic matrix. The direct observation of the mixed monolayer morphology by Brewster angle microscopy (BAM) strongly suggests that DNA adsorption induces a reorganization of lipids at the interface, as evidenced by the change in the condensed lipidic domains morphology in the presence of DNA in the subphase. The immobilization of various polynucleotidie probes of 4000, 400 and 22 base length, confirmed by fluorescence microscopy, had similar effects on DOGS interfacial properties. Preliminary studies are finally presented to explore the possibility of using this system for the study of hybridization between complementary strands. Hence, this study demonstrates this functionalized matrix behaves as a fluid support where polynucleotide immobilization induces interfacial properties modifications, which could be further exploited through the experimental characterization of Faraday instabilities sensitive to visco-elasticity variations. (C) 2004 Elsevier B.V. All rights reserved.
机译:这项工作基于对专门为多核苷酸固定化而设计的活性脂质基质的界面性质的研究,提出了一种直接检测空气-水界面处的聚电解质的新方法。具有阳离子精胺头基的合成脂质DiOctadecylamidoGlycylSpermine(DOGS)在界面处铺展,形成能够捕获多核苷酸的可变形薄膜。通过记录表面压力区域(pi-A)等温线图,呈现特定形状,在纯水子相上具有典型的液体膨胀-液体冷凝相变,可以控制压缩后该功能化单分子层的组织状态。在亚相中存在各种dsDNA浓度的情况下,等温线以时间和浓度依赖性方式显着改变。通过对单层可压缩性曲线的精细分析,证实了与较大分子区域发生较大变化和相变明显消失相对应的主要修饰,从而表明了随时间和时间变化的单层流动性特征变化。 DNA浓度。此外,ATR-傅立叶变换红外(ATR-FTIR)表征显示了DNA链吸附在脂质基质上的证据。通过布鲁斯特角显微镜(BAM)对混合单分子层形态的直接观察强烈表明,DNA吸附在界面处诱导脂质重组,这由亚相中存在DNA时浓缩的脂质域形态变化所证明。荧光显微镜确认的4000、400和22个碱基长的各种多核苷酸探针的固定化对DOGS界面性质具有相似的影响。最后提出了初步研究,以探索使用该系统研究互补链之间杂交的可能性。因此,这项研究表明该功能化的基质可作为流体支持物,多核苷酸固定化可引起界面性质的修饰,可通过对粘弹性变化敏感的法拉第不稳定性的实验表征进一步加以利用。 (C)2004 Elsevier B.V.保留所有权利。

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