Embedding and immobilizing protein molecules into two-dimensional protein arrays for single-molecule imaging by tapping mode atomic force microscopy

被引:7
作者
Furuno, T [1 ]
机构
[1] Keio Univ, Sch Med, Dept Phys, Yokohama, Kanagawa 2238521, Japan
来源
JAPANESE JOURNAL OF APPLIED PHYSICS PART 1-REGULAR PAPERS SHORT NOTES & REVIEW PAPERS | 2000年 / 39卷 / 11期
关键词
AFM; two-dimensional crystal; immobilization; adsorption; air/water interface; ferritin; catalase; streptavidin;
D O I
10.1143/JJAP.39.6435
中图分类号
O59 [应用物理学];
学科分类号
摘要
Soluble proteins, ferritin and catalase, were imaged as single molecules by tapping mode atomic force microscopy (AFM) in water. They were isolated and immobilized in two-dimensional (2D) arrays of smaller proteins. ferritin was embedded in 2D arrays of catalase, and catalase was embedded in streptavidin arrays. In the preparation of each sample, two kinds of proteins were dissolved simultaneously in a buffer solution, and were bound to a surface film of polypeptide spread at the air/buffer interface. The protein-bound film was transferred onto a hydrophobic surface of silicon wafer. The isolated molecules of ferritin and catalase protruded halfway from the surface of 2D arrays of majority constituents. The lateral dimensions of these molecules were of convolution with the cantilever tip with the end radius of similar to3 nm. The characteristic shape or size of ferritin and catalase has been well captured as single molecules. This paper demonstrates that embedding protein molecules into protein arrays is a useful means for immobilizing proteins for single-molecule imaging by AFM.
引用
收藏
页码:6435 / 6440
页数:6
相关论文
共 32 条
[1]   ATOMIC FORCE MICROSCOPE [J].
BINNIG, G ;
QUATE, CF ;
GERBER, C .
PHYSICAL REVIEW LETTERS, 1986, 56 (09) :930-933
[2]   HIGH-RESOLUTION ELECTRON-MICROSCOPY AND SCANNING TUNNELING MICROSCOPY OF NATIVE OXIDES ON SILICON [J].
CARIM, AH ;
DOVEK, MM ;
QUATE, CF ;
SINCLAIR, R ;
VORST, C .
SCIENCE, 1987, 237 (4815) :630-633
[3]   Structures and dynamic motion of laminin-1 as observed by atomic force microscopy [J].
Chen, CH ;
Clegg, DO ;
Hansma, HG .
BIOCHEMISTRY, 1998, 37 (22) :8262-8267
[4]   Submolecular resolution of single macromolecules with atomic force microscopy [J].
Czajkowsky, DM ;
Shao, ZF .
FEBS LETTERS, 1998, 430 (1-2) :51-54
[5]   Staphylococcal α-hemolysin can form hexamers in phospholipid bilayers [J].
Czajkowsky, DM ;
Sheng, ST ;
Shao, ZF .
JOURNAL OF MOLECULAR BIOLOGY, 1998, 276 (02) :325-330
[6]   The vacuolating toxin from Helicobacter pylori forms hexameric pores in lipid bilayers at low pH [J].
Czajkowsky, DM ;
Iwamoto, H ;
Cover, TL ;
Shao, ZF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (05) :2001-2006
[7]   IMAGING GLOBULAR AND FILAMENTOUS PROTEINS IN PHYSIOLOGICAL BUFFER SOLUTIONS WITH TAPPING MODE ATOMIC-FORCE MICROSCOPY [J].
FRITZ, M ;
RADMACHER, M ;
CLEVELAND, JP ;
ALLERSMA, MW ;
STEWART, RJ ;
GIESELMANN, R ;
JANMEY, P ;
SCHMIDT, CF ;
HANSMA, PK .
LANGMUIR, 1995, 11 (09) :3529-3535
[8]   DENATURATION OF PURPLE MEMBRANES AT THE AIR-WATER-INTERFACE STUDIED BY SEM [J].
FURUNO, T ;
SASABE, H .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1991, 147 (01) :225-232
[9]   2-DIMENSIONAL CRYSTALLIZATION OF STREPTAVIDIN BY NONSPECIFIC-BINDING TO A SURFACE-FILM - STUDY WITH A SCANNING ELECTRON-MICROSCOPE [J].
FURUNO, T ;
SASABE, H .
BIOPHYSICAL JOURNAL, 1993, 65 (04) :1714-1717
[10]   Imaging two-dimensional arrays of soluble proteins by atomic force microscopy in contact mode using a sharp supertip [J].
Furuno, T ;
Sasabe, H ;
Ikegami, A .
ULTRAMICROSCOPY, 1998, 70 (03) :125-131