An effective Coarse‐grained model for biological simulations: Recent refinements and validations. Issue 7 (6th December 2013)
- Record Type:
- Journal Article
- Title:
- An effective Coarse‐grained model for biological simulations: Recent refinements and validations. Issue 7 (6th December 2013)
- Main Title:
- An effective Coarse‐grained model for biological simulations: Recent refinements and validations
- Authors:
- Vicatos, Spyridon
Rychkova, Anna
Mukherjee, Shayantani
Warshel, Arieh - Abstract:
- <abstract abstract-type="main"> <title>ABSTRACT</title> <p>Exploring the free energy landscape of proteins and modeling the corresponding functional aspects presents a major challenge for computer simulation approaches. This challenge is due to the complexity of the landscape and the enormous computer time needed for converging simulations. The use of various simplified coarse grained (CG) models offers an effective way of sampling the landscape, but most current models are not expected to give a reliable description of protein stability and functional aspects. The main problem is associated with insufficient focus on the electrostatic features of the model. In this respect, our recent CG model offers significant advantage as it has been refined while focusing on its electrostatic free energy. Here we review the current state of our model, describing recent refinements, extensions, and validation studies while focusing on demonstrating key applications. These include studies of protein stability, extending the model to include membranes, electrolytes and electrodes, as well as studies of voltage‐activated proteins, protein insertion through the translocon, the action of molecular motors, and even the coupling of the stalled ribosome and the translocon. The examples discussed here illustrate the general potential of our approach in overcoming major challenges in studies of structure function correlation in proteins and large macromolecular complexes. Proteins 2014;<abstract abstract-type="main"> <title>ABSTRACT</title> <p>Exploring the free energy landscape of proteins and modeling the corresponding functional aspects presents a major challenge for computer simulation approaches. This challenge is due to the complexity of the landscape and the enormous computer time needed for converging simulations. The use of various simplified coarse grained (CG) models offers an effective way of sampling the landscape, but most current models are not expected to give a reliable description of protein stability and functional aspects. The main problem is associated with insufficient focus on the electrostatic features of the model. In this respect, our recent CG model offers significant advantage as it has been refined while focusing on its electrostatic free energy. Here we review the current state of our model, describing recent refinements, extensions, and validation studies while focusing on demonstrating key applications. These include studies of protein stability, extending the model to include membranes, electrolytes and electrodes, as well as studies of voltage‐activated proteins, protein insertion through the translocon, the action of molecular motors, and even the coupling of the stalled ribosome and the translocon. The examples discussed here illustrate the general potential of our approach in overcoming major challenges in studies of structure function correlation in proteins and large macromolecular complexes. Proteins 2014; 82:1168–1185. © 2013 Wiley Periodicals, Inc.</p> </abstract> … (more)
- Is Part Of:
- Proteins. Volume 82:Issue 7(2014)
- Journal:
- Proteins
- Issue:
- Volume 82:Issue 7(2014)
- Issue Display:
- Volume 82, Issue 7 (2014)
- Year:
- 2014
- Volume:
- 82
- Issue:
- 7
- Issue Sort Value:
- 2014-0082-0007-0000
- Page Start:
- 1168
- Page End:
- 1185
- Publication Date:
- 2013-12-06
- Subjects:
- Proteins -- Periodicals
Proteins -- Periodicals
572.6 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/prot.24482 ↗
- Languages:
- English
- ISSNs:
- 0887-3585
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6936.164000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3714.xml