The structure of the V1-ATPase determined by three-dimensional electron microscopy of single particles

Michael Radermacher*, Teresa Ruiz, Helmut Wieczorek, Gerhard Grüber

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

95 Citations (Scopus)

Abstract

We determined the structure of the V1-ATPase from Manduca sexta to a resolution of 1.8 nm, which for the first time reveals internal features of the enzyme. The V1-ATPase consists of a headpiece of 13.5 nm in diameter, with six elongated subunits, A3 and B3, of approximately equal size, and a stalk of 6 nm in length that connects V1 with the membrane-bound domain, VO. At the center of the molecule is a cavity that extends throughout the length of the A3B3 hexamer. Inside the cavity the central stalk can be seen connected to only two of the catalytic A subunits. The structure was obtained by a combination of the Random Conical Reconstruction Technique and angular refinements. Additional recently developed techniques that were used include methods for simultaneous translational rotational alignment of the 0° images, contrast transfer function correction for tilt images, and the Two-Step Radon Inversion Algorithm.

Original languageEnglish
Pages (from-to)26-37
Number of pages12
JournalJournal of Structural Biology
Volume135
Issue number1
DOIs
Publication statusPublished - 2001
Externally publishedYes

ASJC Scopus Subject Areas

  • Structural Biology

Keywords

  • CTF correction
  • Electron microscopy
  • HV-ATPase
  • Manduca sexta
  • Radon transforms
  • Simultaneous alignment
  • Three-dimensional reconstruction
  • Vacuolar-type ATPase

Fingerprint

Dive into the research topics of 'The structure of the V1-ATPase determined by three-dimensional electron microscopy of single particles'. Together they form a unique fingerprint.

Cite this