A study of cytokinetic and motile prostate cancer cells using synchrotron-based FTIR micro spectroscopic imaging

被引:54
作者
Gazi, E
Dwyer, J
Lockyer, NP
Miyan, J
Gardner, P
Hart, CA
Brown, MD
Clarke, NW
机构
[1] Univ Manchester, Sch Chem Engn & Analyt Sci, Manchester M60 1QD, Lancs, England
[2] Univ Manchester, Fac Life Sci, Manchester M60 1QD, Lancs, England
[3] Christie Hosp NHS Trust, ProMPT Genito Urinary Canc Res Grp, Canc Res UK, Paterson Inst, Manchester M20 4BX, Lancs, England
[4] Hope Hosp, NHS Trust, Dept Urol, Salford M6 8HD, Lancs, England
关键词
prostate cancer; cytokinesis; motility; FTIR microspectroscopy; synchrotron;
D O I
10.1016/j.vibspec.2005.02.026
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Synchrotron-based Fourier transform infrared (SR-FTIR) microspectroscopy has been applied to the study of dynamic cellular events. SR-FTIR microspectroscopy is a powerful bioanalytical technique for the simultaneous analysis of proteins, lipids and a variety of phosphorylated molecules within whole cells. In this study, SR-FTIR microspectroscopy was used in imaging mode to generate biospectroscopic chemical maps of formalin-fixed PC-3 prostate cancer cells, which had been preserved in the process of cell division (cytokinesis) and locomotion. The distribution and intensity profiles of IR signals corresponding to the amide I and 11 (protein) and/or v(as and s) (CH3), v(as and s) (CH2) (lipid) modes were found to be useful in understanding fundamental biochemical processes at the midbody of the cytokinetic cells and at the lamellipodium of motile cells. Furthermore, in both of these cellular systems we observed a distinct hemispherical distribution of the lipid ester (C=O) signal, which surrounded high phosphate signal. This feature was assigned to intracellular IR signals corresponding to membrane-rich organelles surrounding the cell nucleus. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:193 / 201
页数:9
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