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用于原子力显微镜研究的活细胞阵列的生成。

Generation of living cell arrays for atomic force microscopy studies.

机构信息

1] Centre Nationale de la Recherche Scientifique (CNRS), Laboratoire d'Analyse et d'Architecture des Systèmes (LAAS), Toulouse, France. [2] Université de Toulouse; LAAS, Institut des Technologies Avancées en Sciences du Vivant (ITAV), Institute de Pharmacologie et de Biologie Structurale (IPBS), Toulouse, France. [3] CNRS, Unité Mixte de Recherche (UMR) 7565, Laboratoire Structure et Réactivité des Systèmes Moléculaires Complexes (SRSMC), Vandœuvre-lès-Nancy, France. [4] Université de Lorraine, UMR 7565, Faculté de Pharmacie, Nancy, France.

1] Université de Toulouse; LAAS, Institut des Technologies Avancées en Sciences du Vivant (ITAV), Institute de Pharmacologie et de Biologie Structurale (IPBS), Toulouse, France. [2] CNRS, IPBS, UMR 5089, Toulouse, France.

出版信息

Nat Protoc. 2015 Jan;10(1):199-204. doi: 10.1038/nprot.2015.004. Epub 2014 Dec 31.

Abstract

Atomic force microscopy (AFM) is a useful tool for studying the morphology or the nanomechanical and adhesive properties of live microorganisms under physiological conditions. However, to perform AFM imaging, living cells must be immobilized firmly enough to withstand the lateral forces exerted by the scanning tip, but without denaturing them. This protocol describes how to immobilize living cells, ranging from spores of bacteria to yeast cells, into polydimethylsiloxane (PDMS) stamps, with no chemical or physical denaturation. This protocol generates arrays of living cells, allowing statistically relevant measurements to be obtained from AFM measurements, which can increase the relevance of results. The first step of the protocol is to generate a microstructured silicon master, from which many microstructured PDMS stamps can be replicated. Living cells are finally assembled into the microstructures of these PDMS stamps using a convective and capillary assembly. The complete procedure can be performed in 1 week, although the first step is done only once, and thus repeats can be completed within 1 d.

摘要

原子力显微镜(AFM)是一种用于在生理条件下研究活微生物的形态或纳米力学和粘附特性的有用工具。然而,为了进行 AFM 成像,必须将活细胞固定得足够牢固,以承受扫描针尖施加的侧向力,但又不能使它们变性。本方案描述了如何将活细胞(从细菌孢子到酵母细胞)固定在聚二甲基硅氧烷(PDMS)印模中,而不会发生化学或物理变性。本方案生成活细胞阵列,允许从 AFM 测量中获得具有统计学意义的测量结果,从而提高结果的相关性。该方案的第一步是生成微结构硅母版,可从中复制许多微结构 PDMS 印模。最后,使用对流和毛细组装将活细胞组装到这些 PDMS 印模的微结构中。完整的过程可以在 1 周内完成,尽管第一步仅进行一次,因此可以在 1 天内完成重复步骤。

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