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New invention unravels mystery of protein folding

Date:
September 14, 2011
Source:
DOE/Oak Ridge National Laboratory
Summary:
A new invention able to quickly predict three-dimensional structure of protein could have huge implications for drug discovery and human health.
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An Oak Ridge National Laboratory invention able to quickly predict three-dimensional structure of protein could have huge implications for drug discovery and human health.

While scientists have long studied protein structure and the mechanism of folding, this marks the first time they are able to computationally predict three-dimensional structure independent of size of the protein. Because the invention also determines possible intermediate states in the protein folding process, it provides a clearer picture and could open doors to designing new medicines for neurodegenerative diseases that are caused by incorrectly folded proteins.

Pratul Agarwal, inventor of the method and a member of the Department of Energy lab's Computer Science and Mathematics Division, believes this new method will provide benefits in many areas.

"This finding is relevant to energy, climate and health, which are all of tremendous significance today," Agarwal said. "We expect this approach to have many industrial applications through protein engineering, for example, where we expect to be able to design more efficient enzymes."

Proteins often adopt a three-dimensional structure that allows them to carry out their designated function, but such a structure has provided a computationally challenging task. Using the fundamental insights of the protein structure, dynamics and function, the ORNL invention discloses a unique computational methodology to explore the conformational energy landscape of a protein.

"One of the main advantages of this approach is that it follows the natural intrinsic dynamics of the protein and by promoting the relevant dynamical modes allows rapid exploration of the folding pathway and prediction of the protein structure," Agarwal said.

In the area of drug development, Agarwal, a computational biophysicist, expects this discovery to help in the development of treatments with little or no side effects.

Funding for this research has been provided by the National Institutes of Health, Battelle Memorial Institute and the ORNL Laboratory Directed Research and Development program. Patent No. 7,983,887, "Fast computational methods for mechanism of protein folding and prediction of protein structure from primary sequence," was issued to Agarwal in July 2011.


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The above post is reprinted from materials provided by DOE/Oak Ridge National Laboratory. Note: Materials may be edited for content and length.


Journal References:

  1. Arvind Ramanathan, Andrej J. Savol, Christopher J. Langmead, Pratul K. Agarwal, Chakra S. Chennubhotla. Discovering Conformational Sub-States Relevant to Protein Function. PLoS ONE, 2011; 6 (1): e15827 DOI: 10.1371/journal.pone.0015827
  2. Jose M. Borreguero, Junhong He, F. Meilleur, Kevin L. Weiss, Craig M. Brown, Dean A. Myles, Kenneth W. Herwig, Pratul K. Agarwal. Redox-Promoting Protein Motions in Rubredoxin. The Journal of Physical Chemistry B, 2011; 115 (28): 8925 DOI: 10.1021/jp201346x

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DOE/Oak Ridge National Laboratory. "New invention unravels mystery of protein folding." ScienceDaily. ScienceDaily, 14 September 2011. <www.sciencedaily.com/releases/2011/09/110914131357.htm>.
DOE/Oak Ridge National Laboratory. (2011, September 14). New invention unravels mystery of protein folding. ScienceDaily. Retrieved July 29, 2015 from www.sciencedaily.com/releases/2011/09/110914131357.htm
DOE/Oak Ridge National Laboratory. "New invention unravels mystery of protein folding." ScienceDaily. www.sciencedaily.com/releases/2011/09/110914131357.htm (accessed July 29, 2015).

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