BioPhotonics workstation: A versatile setup for simultaneous optical manipulation, heat stress, and intracellular pH measurements of a live yeast cell

被引:3
作者
Aabo, Thomas [1 ]
Banas, Andrew Raphael [2 ]
Gluckstad, Jesper [2 ]
Siegumfeldt, Henrik [1 ]
Arneborg, Nils [1 ]
机构
[1] Univ Copenhagen, Dept Food Sci, DK-1958 Frederiksberg C, Denmark
[2] Tech Univ Denmark, DTU Fotonik, Dept Photon Engn, DK-2700 Lyngby, Denmark
关键词
SACCHAROMYCES-CEREVISIAE; FLUORESCENT INDICATORS; ESCHERICHIA-COLI; DEPENDENCE;
D O I
10.1063/1.3625274
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
In this study we have modified the BioPhotonics workstation (BWS), which allows for using long working distance objective for optical trapping, to include traditional epi-fluorescence microscopy, using the trapping objectives. We have also added temperature regulation of sample stage, allowing for fast temperature variations while trapping. Using this modified BWS setup, we investigated the internal pH (pH(i)) response and membrane integrity of an optically trapped Saccharomyces cerevisiae cell at 5 mW subject to increasing temperatures. The pH(i) of the cell is obtained from the emission of 5-(and-6)-carboxyfluorescein diacetate, succinimidyl ester, at 435 and 485 nm wavelengths, while the permeability is indicated by the fluorescence of propidium iodide. We present images mapping the pH(i) and permeability of the cell at different temperatures and with enough spatial resolution to localize these attributes within the cell. The combined capability of optical trapping, fluorescence microscopy and temperature regulation offers a versatile tool for biological research. (C) 2011 American Institute of Physics. [doi:10.1063/1.3625274]
引用
收藏
页数:6
相关论文
共 23 条
[1]   Effect of long- and short-term exposure to laser light at 1070 nm on growth of Saccharomyces cerevisiae [J].
Aabo, Thomas ;
Perch-Nielsen, Ivan R. ;
Dam, Jeppe Seidelin ;
Palima, Darwin Z. ;
Siegumfeldt, Henrik ;
Gluckstad, Jesper ;
Arneborg, Nils .
JOURNAL OF BIOMEDICAL OPTICS, 2010, 15 (04)
[2]   ACCELERATION AND TRAPPING OF PARTICLES BY RADIATION PRESSURE [J].
ASHKIN, A .
PHYSICAL REVIEW LETTERS, 1970, 24 (04) :156-&
[3]   Determination of the intracellular pH (pHi) of growing cells of Saccharomyces cerevisiae:: the effect of reduced-expression of the membrane H+-ATPase [J].
Bracey, D ;
Holyoak, CD ;
Nebe-von Caron, G ;
Coote, PJ .
JOURNAL OF MICROBIOLOGICAL METHODS, 1998, 31 (03) :113-125
[4]   Assessment of the intracellular pH of immobilized and continuously perfused yeast cells employing fluorescence ratio imaging analysis [J].
Breeuwer, P ;
Abee, T .
JOURNAL OF MICROBIOLOGICAL METHODS, 2000, 39 (03) :253-264
[5]  
BRIGHT G, 1989, METHODS CELL BIOL FL, P157
[6]   Optical micromanipulation [J].
Dholakia, Kishan ;
Reece, Peter ;
Gu, Min .
CHEMICAL SOCIETY REVIEWS, 2008, 37 (01) :42-55
[7]   MEASUREMENT OF YEAST INTRACELLULAR PH BY IMAGE-PROCESSING AND THE CHANGE IT UNDERGOES DURING GROWTH-PHASE [J].
IMAI, T ;
OHNO, T .
JOURNAL OF BIOTECHNOLOGY, 1995, 38 (02) :165-172
[8]   AN IMPROVED METHOD TO DETERMINE CELL VIABILITY BY SIMULTANEOUS STAINING WITH FLUORESCEIN DIACETATE PROPIDIUM IODIDE [J].
JONES, KH ;
SENFT, JA .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1985, 33 (01) :77-79
[9]   Wavelength dependence of cell cloning efficiency after optical trapping [J].
Liang, H ;
Vu, KT ;
Krishnan, P ;
Trang, TC ;
Shin, D ;
Kimel, S ;
Berns, MW .
BIOPHYSICAL JOURNAL, 1996, 70 (03) :1529-1533
[10]   PH-DEPENDENCE OF FLUORESCEIN FLUORESCENCE [J].
MARTIN, MM ;
LINDQVIST, L .
JOURNAL OF LUMINESCENCE, 1975, 10 (06) :381-390