Abundance of Escherichia coli F1-ATPase molecules observed to rotate via single-molecule microscopy with gold nanorod probes

被引:0
|
作者
Justin York
David Spetzler
Tassilo Hornung
Robert Ishmukhametov
James Martin
Wayne D. Frasch
机构
[1] Arizona State University,School of Life Sciences
来源
Journal of Bioenergetics and Biomembranes | 2007年 / 39卷
关键词
F; -ATPase; Gold nanorods; Plasmon resonance; Molecular motors; Single molecule microscopy;
D O I
暂无
中图分类号
学科分类号
摘要
The abundance of E. coli F1-ATPase molecules observed to rotate using gold nanorods attached to the γ-subunit was quantitated. Individual F1 molecules were determined to be rotating based upon time dependent fluctuations of red and green light scattered from the nanorods when viewed through a polarizing filter. The average number of F1 molecules observed to rotate in the presence of GTP, ATP, and without nucleotide was ∼50, ∼25, and ∼4% respectively. In some experiments, the fraction of molecules observed to rotate in the presence of GTP was as high as 65%. These data indicate that rotational measurements made using gold nanorods provide information of the F1-ATPase mechanism that is representative of the characteristics of the enzyme population as a whole.
引用
收藏
页码:435 / 439
页数:4
相关论文
共 47 条
  • [1] Abundance of Escherichia coli F1-ATPase molecules observed to rotate via single-molecule microscopy with gold nanorod probes
    York, Justin
    Spetzler, David
    Hornung, Tassilo
    Ishmukhametov, Robert
    Martin, James
    Frasch, Wayne D.
    JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 2007, 39 (5-6) : 435 - 439
  • [2] Giant Acceleration of Diffusion Observed in a Single-Molecule Experiment on F1-ATPase
    Hayashi, Ryunosuke
    Sasaki, Kazuo
    Nakamura, Shuichi
    Kudo, Seishi
    Inoue, Yuichi
    Noji, Hiroyuki
    Hayashi, Kumiko
    PHYSICAL REVIEW LETTERS, 2015, 114 (24)
  • [3] High-resolution single-molecule characterization of the enzymatic states in Escherichia coli F1-ATPase
    Bilyard, Thomas
    Nakanishi-Matsui, Mayumi
    Steel, Bradley C.
    Pilizota, Teuta
    Nord, Ashley L.
    Hosokawa, Hiroyuki
    Futai, Masamitsu
    Berry, Richard M.
    PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2013, 368 (1611)
  • [4] Single-molecule detection of DNA via sequence-specific links between F1-ATPase motors and gold nanorod sensors
    York, Justin
    Spetzler, David
    Xiong, Fusheng
    Frasch, Wayne D.
    LAB ON A CHIP, 2008, 8 (03) : 415 - 419
  • [5] Single-molecule imaging of rotation of F1-ATPase
    Adachi, K
    Noji, H
    Kinosita, K
    BIOPHOTONICS, PT B, 2003, 361 : 211 - 227
  • [6] Biochemical and single-molecule analyses of human F1-ATPase
    Suzuki, Toshiharu
    Wakabayashi, Chiaki
    Salta, Ei-ichiro
    Tanaka, Kazumi
    Furuike, Shou
    Kinosita, Kazuhiko, Jr.
    Yoshida, Masasuke
    BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2010, 1797 : 38 - 39
  • [7] Single-molecule analysis of bovine mitochondrial F1-ATPase
    Kobayashi, R.
    Ueno, H.
    Suzuki, T.
    Hara, M.
    Noji, H.
    EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 2017, 46 : S132 - S132
  • [8] Single-molecule imaging of the rotation and multisite catalysis F1-ATPase
    Aclachi, K
    Nishizaka, T
    Noji, H
    Itoh, H
    Oiwa, K
    Yoshida, M
    Kinosita, K
    BIOPHYSICAL JOURNAL, 2004, 86 (01) : 476A - 476A
  • [9] MEASUREMENT OF THE CONFORMATIONAL STATE OF F1-ATPASE BY SINGLE-MOLECULE ROTATION
    Okuno, Daichi
    Ikeguchi, Mitsunori
    Noji, Hiroyuki
    METHODS IN ENZYMOLOGY, VOL 475: SINGLE MOLECULE TOOLS, PT B: SUPER-RESOLUTION, PARTICLE TRACKING, MULTIPARAMETER, AND FORCE BASED METHODS, 2010, 475 : 279 - 296
  • [10] THE STRUCTURE OF F1-ATPASE IN ESCHERICHIA-COLI OBSERVED USING STEM
    CURGY, JJ
    COLLIEX, C
    IFTODE, F
    SATRE, M
    VIGNAIS, PV
    BIOLOGY OF THE CELL, 1983, 49 (01) : A30 - A30