首页> 外文期刊>DMW: Deutsche Medizinische Wochenschrift >Physician-patient-family relationship - A core element of a successful intensive care therapy? [Arzt-Patient-Angeh?rigen-Beziehung auf der Intensivstation - Essenzielle Grundlage einer erfolgreichen Therapie?]
【24h】

Physician-patient-family relationship - A core element of a successful intensive care therapy? [Arzt-Patient-Angeh?rigen-Beziehung auf der Intensivstation - Essenzielle Grundlage einer erfolgreichen Therapie?]

机译:医师-患者-家庭关系-成功的重症监护治疗的核心要素? [重症监护室中的医患关系-成功治疗的重要依据?]

获取原文
获取原文并翻译 | 示例
       

摘要

Investigations into the fate of small interfering RNA (siRNA) after transfection may unravel new ways to improve RNA interference (RNAi) efficiency. Because intracellular degradation of RNA may prevent reliable observation of fluorescence- labeled siRNA, new tools for fluorescence microscopy are warranted to cover the considerable duration of the RNAi effect. Here, the characterization and application of new fluorescence resonance energy transfer (FRET) dye pairs for sensing the integrity of duplex siRNA is reported, which allows an assessment of the degradation status of an siRNA cell population by live cell imaging. A panel of high-yield fluorescent dyes has been investigated for their suitability as FRET pairs for the investigation of RNA inside the cell. Nine dyes in 13 FRET pairs were evaluated based on the performance in assays of photostability, cross-excitation, bleedthrough, as well as on quantified changes of fluorescence as a consequence of, e.g., RNA strand hybridization and pH variation. The Atto488/Atto590 FRET pair has been applied to live cell imaging, and has revealed first aspects of unusual trafficking of intact siRNA. A time-lapse study showed highly dynamic movement of siRNA in large perinuclear structures. These and the resulting optimized FRET labeled siRNA are expected to have significant impact on future observations of labeled RNAs in living cells.
机译:转染后对小干扰RNA(siRNA)命运的调查可能会揭示提高RNA干扰(RNAi)效率的新方法。由于RNA的细胞内降解可能阻止可靠地观察荧光标记的siRNA,因此有必要使用新的荧光显微镜检查工具覆盖相当长的RNAi效应。在此,报道了用于检测双链siRNA完整性的新型荧光共振能量转移(FRET)染料对的表征和应用,该染料对可通过活细胞成像评估siRNA细胞群体的降解状态。已经研究了一组高产率荧光染料作为FRET对在细胞内RNA研究中的适用性。根据光稳定性,交叉激发,渗漏分析的性能以及由于RNA链杂交和pH值变化引起的荧光定量变化,对13对FRET中的9种染料进行了评估。 Atto488 / Atto590 FRET对已应用于活细胞成像,并揭示了完整siRNA异常转运的最初方面。一项延时研究显示,siRNA在大核周结构中具有高度动态的运动。这些以及由此产生的优化的FRET标记的siRNA预计将对活细胞中标记RNA的未来观察产生重大影响。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号