Lipid nanotube encapsulating method for two- and three-dimensional transmission electron microscopy analyses of cage-shaped proteins

被引:11
作者
Furusho, Hirotoshi [1 ,2 ]
Mishima, Yumiko [3 ]
Kameta, Norihiro [4 ]
Masuda, Mitsutoshi [4 ,5 ]
Yamashita, Ichiro [2 ,3 ,6 ]
Shimizu, Toshimi [4 ,5 ]
机构
[1] Osaka Univ, Res Ctr Ultra High Voltage Electron Microscopy, Osaka 5670047, Japan
[2] Nara Inst Sci & Technol, Grad Sch Mat Sci, Nara 6300192, Japan
[3] Japan Sci & Technol Agcy, CREST, Kawaguchi, Saitama 3320012, Japan
[4] Japan Sci & Technol Agcy, SORST, Tsukuba, Ibaraki 3058565, Japan
[5] Natl Inst Adv Ind Sci & Technol, Nanoarchitecton Res Ctr NARC, Tsukuba, Ibaraki 3058565, Japan
[6] Matsushita Elect Ind Co Ltd, Adv Technol Res Labs, Kyoto 6190237, Japan
关键词
transmission electron microscopy; sample fixation; electron tomography; EELS mapping; glycolipid nanotube; ferritin; Dps;
D O I
10.1143/JJAP.47.394
中图分类号
O59 [应用物理学];
学科分类号
摘要
A novel, sample-fixation technique for transmission electron microscopy (TEM) is proposed. We encapsulated various samples in one-dimensional hollow cylinders of a glycolipid nanotube (LNT) and found it to be highly stable, flexible, and reproducible. The cylindrical shape of the LNT allows us to observe nanomaterials consistently even when the samples are rotated around the tube axis. This is critical in improving TEM computed tomography (CT), which suffers from the loss of the electron beam at high tilting angles because of the increased effective thickness of the supporting film. This technique makes it possible to reconstruct three-dimensional images from weak-signal TEM images. In this work, we examined two types of cage-shaped proteins, ferritin, and DNA-binding protein from starved cells (Dps). We reconstructed three-dimensional images of Fe cores from zero-loss images or from electron energy-loss spectroscopy (EELS) mapping images obtained with the Fe M(2.3) edge. We also applied negative staining and vitreous ice embedding (VIE). These results show the potential of the LNT encapsulation technique.
引用
收藏
页码:394 / 399
页数:6
相关论文
共 10 条
[1]   Ferritins: Molecular properties, iron storage function and cellular regulation [J].
Harrison, PM ;
Arosio, P .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1996, 1275 (03) :161-203
[2]   Iron incorporation into Escherichia coli Dps gives rise to a ferritin-like microcrystalline core [J].
Ilari, A ;
Ceci, P ;
Ferrari, D ;
Rossi, GL ;
Chiancone, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (40) :37619-37623
[3]   Selective construction of supramolecular nanotube hosts with cationic inner surfaces [J].
Kameta, N ;
Masuda, M ;
Minamikawa, H ;
Goutev, NV ;
Rim, JA ;
Jung, JH ;
Shimizu, T .
ADVANCED MATERIALS, 2005, 17 (22) :2732-+
[4]   Imaging of single organic molecules in motion [J].
Koshino, Masanori ;
Tanaka, Takatsugu ;
Solin, Niclas ;
Suenaga, Kazutomo ;
Isobe, Hiroyuki ;
Nakamura, Eiichi .
SCIENCE, 2007, 316 (5826) :853-853
[5]   3D electron microscopy in the physical sciences: the development of Z-contrast and EFTEM tomography [J].
Midgley, PA ;
Weyland, M .
ULTRAMICROSCOPY, 2003, 96 (3-4) :413-431
[6]   Supramolecular nanotube architectures based on amphiphilic molecules [J].
Shimizu, T ;
Masuda, M ;
Minamikawa, H .
CHEMICAL REVIEWS, 2005, 105 (04) :1401-1443
[7]  
SHINDO D, 2002, ANAL ELECT MICROSCOP, pCH3
[8]   ION CHANNEL OF ACETYLCHOLINE-RECEPTOR RECONSTRUCTED FROM IMAGES OF POSTSYNAPTIC MEMBRANES [J].
TOYOSHIMA, C ;
UNWIN, N .
NATURE, 1988, 336 (6196) :247-250
[9]   ON THE USE OF HOLEY GRIDS IN ELECTRON CRYSTALLOGRAPHY [J].
TOYOSHIMA, C .
ULTRAMICROSCOPY, 1989, 30 (03) :439-443
[10]   Lipid nanotubes as substrates for helical crystallization of macromolecules [J].
Wilson-Kubalek, EM ;
Brown, RE ;
Celia, H ;
Milligan, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (14) :8040-8045