Synchrotron macro ATR-FTIR microspectroscopy for high-resolution chemical mapping of single cells

被引:86
作者
Vongsvivut, Jitraporn [1 ]
Perez-Guaita, David [2 ]
Wood, Bayden R. [2 ]
Heraud, Philip [2 ,3 ,4 ]
Khambatta, Karma [5 ,6 ]
Hartnell, David [5 ,6 ]
Hackett, Mark J. [5 ,6 ]
Tobin, Mark J. [1 ]
机构
[1] Australian Synchrotron, Infrared Microspect IRM Beamline, 800 Blackburn Rd, Clayton, Vic 3168, Australia
[2] Monash Univ, Ctr Biospect, Clayton, Vic 3168, Australia
[3] Monash Univ, Dept Microbiol, Clayton, Vic 3168, Australia
[4] Monash Univ, Biomed Discovery Inst, Clayton, Vic 3168, Australia
[5] Curtin Univ, Sch Mol & Life Sci, Curtin Inst Funct Mol & Interfaces, GPO Box U1987, Perth, WA 6845, Australia
[6] Curtin Univ, Curtin Hlth Innovat Res Inst, GPO Box U1987, Perth, WA 6845, Australia
基金
澳大利亚研究理事会; 欧洲研究理事会;
关键词
INTERNAL-REFLECTION ELEMENT; INFRARED MICROSPECTROSCOPY; SPATIAL-RESOLUTION; PLANT; DIFFERENTIATION; SPECTROSCOPY; SURFACES; TISSUE;
D O I
10.1039/c8an01543k
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy has been used widely for probing the molecular properties of materials. Coupling a synchrotron infrared (IR) beam to an ATR element using a high numerical aperture (NA) microscope objective enhances the spatial resolution, relative to transmission or transflectance microspectroscopy, by a factor proportional to the refractive index (n) of the ATR element. This work presents the development of the synchrotron macro ATR-FTIR micro-spectroscopy at Australian Synchrotron Infrared Microspectroscopy (IRM) Beamline, and demonstrates that high quality FTIR chemical maps of single cells and tissues can be achieved at an enhanced spatial resolution. The so-called "hybrid" macro ATR-FTIR device was developed by modifying the cantilever arm of a standard Bruker macro ATR-FTIR unit to accept germanium (Ge) ATR elements with different facet sizes (i.e. 1 mm, 250 mu m and 100 mu m in diameter) suitable for different types of sample surfaces. We demonstrated the capability of the technique for high-resolution single cell analysis of malaria-infected red blood cells, individual neurons in a brain tissue and cellular structures of a Eucalyptus leaf. The ability to measure a range of samples from soft membranes to hard cell wall structures demonstrates the potential of the technique for high-resolution chemical mapping across a broad range of applications in biology, medicine and environmental science.
引用
收藏
页码:3226 / 3238
页数:13
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