A high-speed atomic force microscope for studying biological macromolecules in action

被引:93
作者
Ando, T [1 ]
Kodera, N
Maruyama, D
Takai, E
Saito, K
Toda, A
机构
[1] Kanazawa Univ, Fac Sci, Dept Phys, Kanazawa, Ishikawa 1921192, Japan
[2] Olympus Co, Hachioji, Tokyo 1928507, Japan
来源
JAPANESE JOURNAL OF APPLIED PHYSICS PART 1-REGULAR PAPERS SHORT NOTES & REVIEW PAPERS | 2002年 / 41卷 / 7B期
关键词
AFM; protein; biomolecules; real-time imaging; dynamics;
D O I
10.1143/JJAP.41.4851
中图分类号
O59 [应用物理学];
学科分类号
摘要
The atomic force microscope (AFM) is a powerful tool for imaging biological molecules on a substrate, in solution. However, there is no effective time axis with AFM; commercially available AFMs require minutes to capture an image, but many interesting biological processes occur at a much higher rate. Hence, what we can observe using the AFM is limited to stationary molecules, or those moving very slowly. We sought to increase markedly the scan speed of the AFM, so that in the future it can be used to study the dynamic behavior of biomolecules. For this purpose, we have developed various devices optimized for high-speed scanning. Combining these devices has produced an AFM that can capture a 100 x 100 pixel image within 80 ms, thus generating a movie consisting of many successive images of a sample in aqueous solution. This is demonstrated by imaging myosin V molecules moving on mica, in solution.
引用
收藏
页码:4851 / 4856
页数:6
相关论文
共 10 条
[1]   A high-speed atomic force microscope for studying biological macromolecules [J].
Ando, T ;
Kodera, N ;
Takai, E ;
Maruyama, D ;
Saito, K ;
Toda, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (22) :12468-12472
[2]   IMAGING STEEP, HIGH STRUCTURES BY SCANNING FORCE MICROSCOPY WITH ELECTRON-BEAM DEPOSITED TIPS [J].
KELLER, DJ ;
CHOU, CC .
SURFACE SCIENCE, 1992, 268 (1-3) :333-339
[3]   Parallel atomic force microscopy using cantilevers with integrated piezoresistive sensors and integrated piezoelectric actuators [J].
Minne, SC ;
Manalis, SR ;
Quate, CF .
APPLIED PHYSICS LETTERS, 1995, 67 (26) :3918-3920
[4]   TAPPING MODE ATOMIC-FORCE MICROSCOPY IN LIQUID [J].
PUTMAN, CAJ ;
VANDERWERF, KO ;
DEGROOTH, BG ;
VANHULST, NF ;
GREVE, J .
APPLIED PHYSICS LETTERS, 1994, 64 (18) :2454-2456
[5]   Direct observation of processive movement by individual myosin V molecules [J].
Sakamoto, T ;
Amitani, I ;
Yokota, E ;
Ando, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 272 (02) :586-590
[6]  
SARID D, 1991, SCANNING FORCE MICRO, pCH1
[7]   High-speed atomic force microscopy in liquid [J].
Sulchek, T ;
Hsieh, R ;
Adams, JD ;
Minne, SC ;
Quate, CF ;
Adderton, DM .
REVIEW OF SCIENTIFIC INSTRUMENTS, 2000, 71 (05) :2097-2099
[8]   Direct observation of single kinesin molecules moving along microtubules [J].
Vale, RD ;
Funatsu, T ;
Pierce, DW ;
Romberg, L ;
Harada, Y ;
Yanagida, T .
NATURE, 1996, 380 (6573) :451-453
[9]   High speed atomic force microscopy of biomolecules by image tracking [J].
van Noort, SJT ;
van der Werf, KO ;
de Grooth, BG ;
Greve, J .
BIOPHYSICAL JOURNAL, 1999, 77 (04) :2295-2303
[10]   Fast imaging and fast force spectroscopy of single biopolymers with a new atomic force microscope designed for small cantilevers [J].
Viani, MB ;
Schäffer, TE ;
Paloczi, GT ;
Pietrasanta, LI ;
Smith, BL ;
Thompson, JB ;
Richter, M ;
Rief, M ;
Gaub, HE ;
Plaxco, KW ;
Cleland, AN ;
Hansma, HG ;
Hansma, PK .
REVIEW OF SCIENTIFIC INSTRUMENTS, 1999, 70 (11) :4300-4303