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双捕获拉曼镊子用于探测相互作用的微生物细胞的动力学和异质性。

Dual-trap Raman tweezers for probing dynamics and heterogeneity of interacting microbial cells.

机构信息

Guangxi Academy of Sciences Biophysics Laboratory Nanning, Guangxi 530003, China.

出版信息

J Biomed Opt. 2010 Nov-Dec;15(6):067008. doi: 10.1117/1.3526357.

Abstract

We report on development of dual-trap Raman tweezers for monitoring cellular dynamics and heterogeneity of interacting living cells suspended in a liquid medium. Dual-beam optical tweezers were combined with Raman spectroscopy, which allows capturing two cells that are in direct contact or closely separated by a few micrometers and simultaneously acquiring their Raman spectra with an imaging CCD spectrograph. As a demonstration, we recorded time-lapse Raman spectra of budding yeast cells held in dual traps for over 40 min to monitor the dynamic growth in a nutrient medium. We also monitored two germinating Bacillus spores after the initiation with L-alanine and observed their heterogeneity in the release of CaDPA under identical microenvironment.

摘要

我们报告了双陷阱拉曼镊子的开发,用于监测悬浮在液体介质中的相互作用活细胞的细胞动力学和异质性。双光束光学镊子与拉曼光谱相结合,允许捕获两个直接接触或通过几微米紧密分离的细胞,并同时用成像 CCD 光谱仪获取它们的拉曼光谱。作为演示,我们记录了在双陷阱中保持 40 多分钟的出芽酵母细胞的时间分辨拉曼光谱,以监测在营养介质中的动态生长。我们还在相同的微环境下监测了用 L-丙氨酸引发的两个发芽的芽孢杆菌孢子,并观察了它们在 CaDPA 释放方面的异质性。

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