Torque, chemistry and efficiency in molecular motors: a study of the rotary–chemical coupling in F1-ATPase. Issue 4 (16th July 2015)
- Record Type:
- Journal Article
- Title:
- Torque, chemistry and efficiency in molecular motors: a study of the rotary–chemical coupling in F1-ATPase. Issue 4 (16th July 2015)
- Main Title:
- Torque, chemistry and efficiency in molecular motors: a study of the rotary–chemical coupling in F1-ATPase
- Authors:
- Mukherjee, Shayantani
Bora, Ram Prasad
Warshel, Arieh - Abstract:
- Abstract: Detailed understanding of the action of biological molecular machines must overcome the challenge of gaining a clear knowledge of the corresponding free-energy landscape. An example for this is the elucidation of the nature of converting chemical energy to torque and work in the rotary molecular motor of F1 -ATPase. A major part of the challenge involves understanding the rotary–chemical coupling from a non-phenomenological structure/energy description. Here we focused on using a coarse-grained model of F1 -ATPase to generate a structure-based free-energy landscape of the rotary–chemical process of the whole system. In particular, we concentrated on exploring the possible impact of the position of the catalytic dwell on the efficiency and torque generation of the molecular machine. It was found that the experimentally observed torque can be reproduced with landscapes that have different positions for the catalytic dwell on the rotary–chemical surface. Thus, although the catalysis is undeniably required for torque generation, the experimentally observed position of the catalytic dwell at 80° might not have a clear advantage for the force generation by F1 -ATPase. This further implies that the rotary–chemical couplings in these biological motors are quite robust and their efficiencies do not depend explicitly on the position of the catalytic dwells. Rather, the specific positioning of the dwells with respect to the rotational angle is a characteristic arising due toAbstract: Detailed understanding of the action of biological molecular machines must overcome the challenge of gaining a clear knowledge of the corresponding free-energy landscape. An example for this is the elucidation of the nature of converting chemical energy to torque and work in the rotary molecular motor of F1 -ATPase. A major part of the challenge involves understanding the rotary–chemical coupling from a non-phenomenological structure/energy description. Here we focused on using a coarse-grained model of F1 -ATPase to generate a structure-based free-energy landscape of the rotary–chemical process of the whole system. In particular, we concentrated on exploring the possible impact of the position of the catalytic dwell on the efficiency and torque generation of the molecular machine. It was found that the experimentally observed torque can be reproduced with landscapes that have different positions for the catalytic dwell on the rotary–chemical surface. Thus, although the catalysis is undeniably required for torque generation, the experimentally observed position of the catalytic dwell at 80° might not have a clear advantage for the force generation by F1 -ATPase. This further implies that the rotary–chemical couplings in these biological motors are quite robust and their efficiencies do not depend explicitly on the position of the catalytic dwells. Rather, the specific positioning of the dwells with respect to the rotational angle is a characteristic arising due to the structural construct of the molecular machine and might not bear any clear connection to the thermodynamic efficiency for the system. … (more)
- Is Part Of:
- Quarterly reviews of biophysics. Volume 48:Issue 4(2015)
- Journal:
- Quarterly reviews of biophysics
- Issue:
- Volume 48:Issue 4(2015)
- Issue Display:
- Volume 48, Issue 4 (2015)
- Year:
- 2015
- Volume:
- 48
- Issue:
- 4
- Issue Sort Value:
- 2015-0048-0004-0000
- Page Start:
- 395
- Page End:
- 403
- Publication Date:
- 2015-07-16
- Subjects:
- rotary-chemical surface, -- F0F1-ATP synthase, -- bioenergetics, -- conformational surface
Biophysics -- Periodicals
571.405 - Journal URLs:
- http://journals.cambridge.org/action/displayJournal?jid=QRB ↗
- DOI:
- 10.1017/S0033583515000050 ↗
- Languages:
- English
- ISSNs:
- 0033-5835
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library HMNTS - ELD Digital store
- Ingest File:
- 1073.xml