Visible, near-infrared, and ultraviolet laser-excited Raman spectroscopy of the monocytes/macrophages (U937) cells

被引:27
作者
Zinin, Pavel V. [1 ]
Misra, Anupam [1 ]
Kamemoto, Lori [2 ]
Yu, Qigui [2 ]
Hu, Ningjie [2 ]
Sharma, Shiv K. [1 ]
机构
[1] Univ Hawaii, Sch Ocean & Earth Sci & Technol, Honolulu, HI 96822 USA
[2] Univ Hawaii, John A Burns Sch Med, Honolulu, HI 96822 USA
关键词
monocytes; Raman scattering; UV resonance Raman spectroscopy; UV-RESONANCE RAMAN; RELEVANT MICROORGANISMS; PROTEIN DISTRIBUTION; IN-VIVO; IDENTIFICATION; VIRUS; DNA; BACTERIA; SPECTRA; ACID;
D O I
10.1002/jrs.2444
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Raman spectra of the monocytes were recorded with laser excitation at 532, 785, 830, and 244 nm. The measurements of the Raman spectra of monocytes excited with visible, near-infrared (NIR), and ultraviolet (UV) lasers lad to the following conclusions. (1) The Raman peak pattern of the monocytes can be easily distinguished from those of HeLa and yeast cells; (2) Positions of the Raman peaks of the dried cell are in coincidence with those of the monocytes in a culture cell media. However, the relative intensities of the peaks are changed: the peak centered around 1045 cm(-1) is strongly intensified. (3) Raman spectra of the dead monocytes are similar to those of living cells with only one exception: the Raman peak centered around 1004 cm(-1) associated with breathing mode of phenylalanine is strongly intensified. The Raman spectra of monocytes excited with 244-nm UV laser were measured on cells in a cell culture medium. A peak centered at 1485 cm(-1) dominates the UV Raman spectra of monocytes. The ratio I-1574/I-1613 for monocytes is found to be around 0.71. This number reflects the ratio between proteins and DNA content inside a cell and it is found to be twice as high as that of E. coli and 5 times as high as that of gram-positive bacteria. Copyright (C) 2009 John Wiley & Sons, Ltd.
引用
收藏
页码:268 / 274
页数:7
相关论文
共 42 条
[1]  
ASHER SA, 1988, ANNU REV PHYS CHEM, V39, P537
[2]   ULTRAVIOLET RAMAN-SPECTROSCOPY CHARACTERIZES CHEMICAL-VAPOR-DEPOSITION DIAMOND FILM GROWTH AND OXIDATION [J].
BORMETT, RW ;
ASHER, SA ;
WITOWSKI, RE ;
PARTLOW, WD ;
LIZEWSKI, R ;
PETTIT, F .
JOURNAL OF APPLIED PHYSICS, 1995, 77 (11) :5916-5923
[3]  
Carter EA, 2001, PRACT SPECTROSC SERI, V24, P421
[4]   COMPARISON OF THE UV RESONANCE RAMAN-SPECTRA OF BACTERIA, BACTERIAL-CELL WALLS, AND RIBOSOMES EXCITED IN THE DEEP UV [J].
CHADHA, S ;
MANOHARAN, R ;
MOENNELOCCOZ, P ;
NELSON, WH ;
PETICOLAS, WL ;
SPERRY, JF .
APPLIED SPECTROSCOPY, 1993, 47 (01) :38-43
[5]   DEEP-ULTRAVIOLET RAMAN EXCITATION PROFILES AND VIBRONIC SCATTERING MECHANISMS OF PHENYLALANINE, TYROSINE, AND TRYPTOPHAN [J].
FODOR, SPA ;
COPELAND, RA ;
GRYGON, CA ;
SPIRO, TG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (15) :5509-5518
[6]   Classification of lactic acid bacteria with UV-resonance Raman spectroscopy [J].
Gaus, K. ;
Roesch, P. ;
Petry, R. ;
Peschke, K. -D. ;
Ronneberger, O. ;
Burkhardt, H. ;
Baumann, K. ;
Popp, J. .
BIOPOLYMERS, 2006, 82 (04) :286-290
[7]   Raman spectroscopic signature of life in a living yeast cell [J].
Huang, YS ;
Karashima, T ;
Yamamoto, M ;
Ogura, T ;
Hamaguchi, H .
JOURNAL OF RAMAN SPECTROSCOPY, 2004, 35 (07) :525-+
[8]   Surface enhanced Raman gene probe for HIV detection [J].
Isola, NR ;
Stokes, DL ;
Vo-Dinh, T .
ANALYTICAL CHEMISTRY, 1998, 70 (07) :1352-1356
[9]   Reduction mechanism of tioglycolic acid on keratin fibers using microspectrophotometry and FT-Raman spectroscopy [J].
Kuzuhara, A ;
Hori, T .
POLYMER, 2003, 44 (26) :7963-7970
[10]   Characterization of microorganisms using UV resonance Raman spectroscopy and chemometrics [J].
López-Díez, EC ;
Goodacre, R .
ANALYTICAL CHEMISTRY, 2004, 76 (03) :585-591