• Something wrong with this record ?

Second harmonic atomic force microscopy imaging of live and fixed mammalian cells

A. Dulebo, J. Preiner, F. Kienberger, G. Kada, C. Rankl, L. Chtcheglova, C. Lamprecht, D. Kaftan, P. Hinterdorfer

. 2009 ; 109 (8) : 1056-1060.

Language English Country Netherlands

Document type Comparative Study, Research Support, Non-U.S. Gov't

Higher harmonic contributions in the movement of an oscillating atomic force microscopy (AFM) cantilever are generated by nonlinear tip-sample interactions, yielding additional information on structure and physical properties such as sample stiffness. Higher harmonic amplitudes are strongly enhanced in liquid compared to the operation in air, and were previously reported to result in better structural resolution in highly organized lattices of proteins in bacterial S-layers and viral capsids [J. Preiner, J. Tang, V. Pastushenko, P. Hinterdorfer, Phys. Rev. Lett. 99 (2007) 046102]. We compared first and second harmonics AFM imaging of live and fixed human lung epithelial cells, and microvascular endothelial cells from mouse myocardium (MyEnd). Phase-distance cycles revealed that the second harmonic phase is 8 times more sensitive than the first harmonic phase with respect to variations in the distance between cantilever and sample surface. Frequency spectra were acquired at different positions on living and fixed cells with second harmonic amplitude values correlating with the sample stiffness. We conclude that variations in sample stiffness and corresponding changes in the cantilever-sample distance, latter effect caused by the finite feedback response, result in second harmonic images with improved contrast and information that is not attainable in the fundamental frequency of an oscillating cantilever.

000      
02953naa 2200421 a 4500
001      
bmc11016830
003      
CZ-PrNML
005      
20121130095540.0
008      
110628s2009 ne e eng||
009      
AR
040    __
$a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a ne
100    1_
$a Dulebo, Alexander. $7 _AN066345
245    10
$a Second harmonic atomic force microscopy imaging of live and fixed mammalian cells / $c A. Dulebo, J. Preiner, F. Kienberger, G. Kada, C. Rankl, L. Chtcheglova, C. Lamprecht, D. Kaftan, P. Hinterdorfer
314    __
$a Institute of Physical Biology, University of South Bohemia, Zamek 136, 37333 Nove Hrady, Czech Republic.
520    9_
$a Higher harmonic contributions in the movement of an oscillating atomic force microscopy (AFM) cantilever are generated by nonlinear tip-sample interactions, yielding additional information on structure and physical properties such as sample stiffness. Higher harmonic amplitudes are strongly enhanced in liquid compared to the operation in air, and were previously reported to result in better structural resolution in highly organized lattices of proteins in bacterial S-layers and viral capsids [J. Preiner, J. Tang, V. Pastushenko, P. Hinterdorfer, Phys. Rev. Lett. 99 (2007) 046102]. We compared first and second harmonics AFM imaging of live and fixed human lung epithelial cells, and microvascular endothelial cells from mouse myocardium (MyEnd). Phase-distance cycles revealed that the second harmonic phase is 8 times more sensitive than the first harmonic phase with respect to variations in the distance between cantilever and sample surface. Frequency spectra were acquired at different positions on living and fixed cells with second harmonic amplitude values correlating with the sample stiffness. We conclude that variations in sample stiffness and corresponding changes in the cantilever-sample distance, latter effect caused by the finite feedback response, result in second harmonic images with improved contrast and information that is not attainable in the fundamental frequency of an oscillating cantilever.
590    __
$a bohemika - dle Pubmed
650    _2
$a zvířata $7 D000818
650    _2
$a pružnost $7 D004548
650    _2
$a endoteliální buňky $x ultrastruktura $7 D042783
650    _2
$a epitelové buňky $7 D004847
650    _2
$a eukaryotické buňky $7 D005057
650    _2
$a lidé $7 D006801
650    _2
$a plíce $x cytologie $7 D008168
650    _2
$a myši $7 D051379
650    _2
$a mikroskopie atomárních sil $x metody $7 D018625
650    _2
$a myokard $x cytologie $7 D009206
655    _2
$a srovnávací studie $7 D003160
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Preiner, Johannes
700    1_
$a Kienberger, Ferry
700    1_
$a Kada, Gerald
700    1_
$a Rankl, Christian
700    1_
$a Chtcheglova, Lilia
700    1_
$a Lamprecht, Constanze
700    1_
$a Kaftan, David. $7 _AN063435
700    1_
$a Hinterdorfer, Peter
773    0_
$t Ultramicroscopy $w MED00004596 $g Roč. 109, č. 8 (2009), s. 1056-1060
910    __
$a ABA008 $b x $y 2
990    __
$a 20110720122136 $b ABA008
991    __
$a 20121130095609 $b ABA008
999    __
$a ok $b bmc $g 864087 $s 726622
BAS    __
$a 3
BMC    __
$a 2009 $x MED00004596 $b 109 $c 8 $d 1056-1060 $m Ultramicroscopy $n Ultramicroscopy
LZP    __
$a 2011-3B09/BBjvme

Find record