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A comprehensive model for the diffusion and hybridization processes of nucleic acid probes in fluorescence in situ hybridization

机译:原位杂交中荧光核酸探针的扩散和杂交过程的综合模型

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摘要

Fluorescence in situ hybridization (FISH) has been extensively used in the past decades for the detection and localization of microorganisms. However, a mechanistic approach of the whole FISH process is still missing, and the main limiting steps for the hybridization to occur remain unclear. In here, FISH is approached as a particular case of a diffusion-reaction kinetics, where molecular probes (MPs) move from the hybridization solution to the target RNA site within the cells. Based on literature models, the characteristic times taken by different MPs to diffuse across multiple cellular barriers, as well as the reaction time associated with the formation of the duplex molecular probe-RNA, were estimated. Structural and size differences at the membrane level of bacterial and animal cells were considered. For bacterial cells, the limiting step for diffusion is likely to be the peptidoglycan layer (characteristic time of 7.94 x 10(2) - 4.39 x 10(3) s), whereas for animal cells, the limiting step should be the diffusion of the probe through the bulk (1.8-5.0 s) followed by the diffusion through the lipid membrane (1 s). The information provided here may serve as a basis for a more rational development of FISH protocols in the future.
机译:在过去几十年中,原位杂交(鱼类)的荧光已经广泛用于微生物的检测和定位。然而,整个鱼类过程的机械方法仍然缺失,并且发生杂交的主要限制步骤仍然不清楚。在此,将鱼类作为特定情况接近扩散反应动力学,其中分子探针(MPS)从杂交溶液移动到细胞内的靶RNA位点。基于文献模型,估计不同MPS在多个细胞屏障中扩散的特征时间,以及与双链分子探针-RNA形成相关的反应时间。考虑了细菌和动物细胞膜水平的结构和尺寸差异。对于细菌细胞,扩散的限制步骤可能是肽聚糖层(特征时间为7.94×10(2) - 4.39×10(3)秒,而对于动物细胞,限制步骤应该是扩散探针通过散装(1.8-5.0),然后通过脂膜(1s)扩散。这里提供的信息可以作为未来进行鱼类协议的更合理发展的基础。

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