HR-MAS of cells: A "cellular water shift" due to water-protein interactions?

被引:20
作者
Aime, S
Bruno, E
Cabella, C
Colombatto, S
Digilio, G
Mainero, V
机构
[1] Univ Turin, Dept Chem, IFM, I-10125 Turin, Italy
[2] Bracco Imaging SPA, I-10010 Colleretto Giacosa, TO, Italy
[3] Univ Turin, Dept Med & Expt Oncol, I-10126 Turin, Italy
关键词
NMR spectroscopy; Magic Angle Spinning (MAS); water; cell suspension; protein;
D O I
10.1002/mrm.20707
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Under HR-MAS conditions, cells are subjected to high centrifugal forces that may cause irreversible cell damage. First, conditions have been defined to monitor and keep to a minimum unwanted effects in HR-MAS spectra arising from the loss of cell integrity. Then, the HR-MAS spectra of reasonably intact cells have been analyzed. Cell suspensions subjected to MAS rates as low as 1 kHz split into a two-compartment system that is composed of a cell-rich phase (H2Oi) and a cell-free phase (H2O0). Each of these phases is characterized by its own water H-1-NMR signal. Transport of water molecules between the cell-rich and cell-free compartments is limited by the very low contact area between the two compartments, and water exchange dynamics consequently fall into the slow exchange limit on the NMR timescale. Since the exchange between the two water populations is "frozen," the separation between the H2O0 and H2Oi water signals (Delta nu(water)) detected in an HR-MAS experiment is not affected by chemical exchange but reflects only chemical differences in the two environments. Different cell lines show a different Delta nu(water), leading to the concept of "cellular water shift." This shift roughly correlates with the cellular protein content, supporting the view that the most important determinant of the cellular water shift is the interaction between water and proteins in the intracellular compartment.
引用
收藏
页码:1547 / 1552
页数:6
相关论文
共 12 条
[1]   Insights into the use of paramagnetic Gd(III) complexes in MR-molecular imaging investigations [J].
Aime, S ;
Cabella, C ;
Colombatto, S ;
Crich, SG ;
Gianolio, E ;
Maggioni, F .
JOURNAL OF MAGNETIC RESONANCE IMAGING, 2002, 16 (04) :394-406
[2]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[3]   Application of high-resolution magic-angle spinning NMR spectroscopy to define the cell uptake of MRI contrast agents [J].
Calabi, L ;
Alfieri, G ;
Biondi, L ;
De Miranda, M ;
Paleari, L ;
Ghelli, S .
JOURNAL OF MAGNETIC RESONANCE, 2002, 156 (02) :222-229
[4]   Isotropic susceptibility shift under MAS:: The origin of the split water resonances in 1H MAS NMR spectra of cell suspensions [J].
Chen, JH ;
Enloe, BM ;
Xiao, Y ;
Cory, DG ;
Singer, S .
MAGNETIC RESONANCE IN MEDICINE, 2003, 50 (03) :515-521
[5]   Direct observation of resolved intracellular and extracellular water signals in intact human red blood cells using H-1 MAS NMR spectroscopy [J].
Humpfer, E ;
Spraul, M ;
Nicholls, AW ;
Nicholson, JK ;
Lindon, JC .
MAGNETIC RESONANCE IN MEDICINE, 1997, 38 (02) :334-336
[6]   31P MAS-NMR of human erythrocytes:: Independence of cell volume from angular velocity [J].
Kuchel, PW ;
Bubb, WA ;
Ramadan, S ;
Chapman, BE ;
Philp, DJ ;
Coen, M ;
Gready, JE ;
Harvey, PJ ;
McLean, AJ ;
Hook, J .
MAGNETIC RESONANCE IN MEDICINE, 2004, 52 (03) :663-668
[7]  
Landis CS, 1999, MAGNET RESON MED, V42, P467, DOI 10.1002/(SICI)1522-2594(199909)42:3<467::AID-MRM9>3.0.CO
[8]  
2-0
[9]   Chemical shift and magnetic susceptibility contributions to the separation of intracellular and supernatant resonances in variable angle spinning NMR spectra of erythrocyte suspensions [J].
Philp, DJ ;
Bubb, WA ;
Kuchel, PW .
MAGNETIC RESONANCE IN MEDICINE, 2004, 51 (03) :441-444
[10]   ACTIVATION OF GLYCOLYSIS BY INSULIN WITH A SEQUENTIAL INCREASE OF THE 6-PHOSPHOFRUCTO-2-KINASE ACTIVITY, FRUCTOSE-2,6-BISPHOSPHATE LEVEL AND PYRUVATE-KINASE ACTIVITY IN CULTURED RAT HEPATOCYTES [J].
PROBST, I ;
UNTHANFECHNER, K .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1985, 153 (02) :347-353