Microfluidic Approaches to Synchrotron Radiation-Based Fourier Transform Infrared (SR-FTIR) Spectral Microscopy of Living Biosystems

被引:35
|
作者
Loutherback, Kevin [1 ]
Birarda, Giovanni [1 ,2 ]
Chen, Liang [1 ]
Holman, Hoi-Ying N. [1 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Berkeley Synchrotron Infrared Struct Biol Program, Berkeley, CA 94720 USA
[2] Elettra Synchrotron Light Lab, SS 14 Km 163-5, I-34149 Trieste, Italy
来源
PROTEIN AND PEPTIDE LETTERS | 2016年 / 23卷 / 03期
关键词
FTIR; live cells; microfabrication; microfluidics; synchrotron radiation; QUANTITATIVE IR SPECTROPHOTOMETRY; WATER H2O SOLUTIONS; FOCAL-PLANE ARRAY; SINGLE-CELL; REAL-TIME; PEPTIDE COMPOUNDS; SACCHAROMYCES-CEREVISIAE; PROTEIN AGGREGATION; HIGH-THROUGHPUT; CANCER-CELLS;
D O I
10.2174/0929866523666160106154035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A long-standing desire in biological and biomedical sciences is to be able to probe cellular chemistry as biological processes are happening inside living cells. Synchrotron radiation-based Fourier transform infrared (SR-FTIR) spectral microscopy is a label-free and nondestructive analytical technique that can provide spatiotemporal distributions and relative abundances of biomolecules of a specimen by their characteristic vibrational modes. Despite great progress in recent years, SR-FTIR imaging of living biological systems remains challenging because of the demanding requirements on environmental control and strong infrared absorption of water. To meet this challenge, microfluidic devices have emerged as a method to control the water thickness while providing a hospitable environment to measure cellular processes and responses over many hours or days. This paper will provide an overview of microfluidic device development for SR-FTIR imaging of living biological systems, provide contrast between the various techniques including closed and open-channel designs, and discuss future directions of development within this area. Even as the fundamental science and technological demonstrations develop, other ongoing issues must be addressed; for example, choosing applications whose experimental requirements closely match device capabilities, and developing strategies to efficiently complete the cycle of development. These will require imagination, ingenuity and collaboration.
引用
收藏
页码:273 / 282
页数:10
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