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Proteins. 2014 Dec;82(12):3298-311. doi: 10.1002/prot.24680. Epub 2014 Nov 11.

Understanding the apparent stator-rotor connections in the rotary ATPase family using coarse-grained computer modeling.

Author information

1
School of Physics and Astronomy, University of Leeds, Leeds, United Kingdom.

Abstract

Advances in structural biology, such as cryo-electron microscopy (cryo-EM) have allowed for a number of sophisticated protein complexes to be characterized. However, often only a static snapshot of a protein complex is visualized despite the fact that conformational change is frequently inherent to biological function, as is the case for molecular motors. Computer simulations provide valuable insights into the different conformations available to a particular system that are not accessible using conventional structural techniques. For larger proteins and protein complexes, where a fully atomistic description would be computationally prohibitive, coarse-grained simulation techniques such as Elastic Network Modeling (ENM) are often employed, whereby each atom or group of atoms is linked by a set of springs whose properties can be customized according to the system of interest. Here we compare ENM with a recently proposed continuum model known as Fluctuating Finite Element Analysis (FFEA), which represents the biomolecule as a viscoelastic solid subject to thermal fluctuations. These two complementary computational techniques are used to answer a critical question in the rotary ATPase family; implicit within these motors is the need for a rotor axle and proton pump to rotate freely of the motor domain and stator structures. However, current single particle cryo-EM reconstructions have shown an apparent connection between the stators and rotor axle or pump region, hindering rotation. Both modeling approaches show a possible role for this connection and how it would significantly constrain the mobility of the rotary ATPase family.

KEYWORDS:

Cryo-EM; ENM; FFEA; PCA; finite element analysis; simulation

PMID:
25174610
DOI:
10.1002/prot.24680
[Indexed for MEDLINE]
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