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ShareSep. 11, 2012 — The study of an oxygen-sensing bacterial regulatory protein by chemistry researchers at the University of Georgia has provided molecular insight into the oxygen sensing mechanism, which could ultimately lead to a better understanding of the aging process and new treatments for human diseases such cancer, Parkinson's and Alzheimer's.
Michael Johnson, a distinguished research professor of chemistry in the UGA Franklin College of Arts and Sciences, and Bo Zhang, a UGA chemistry doctoral candidate, have discovered that the fumarate and nitrate reduction regulatory protein, or FNR, in E. coli senses oxygen by a new type of reversible structural change in an iron-sulfur cluster. The work was carried out in collaboration with Nick Le Brun and coworkers from the University of East Anglia. The results were published Sept. 10 in the Proceedings of the National Academy of Sciences.
Iron-sulfur clusters are abundant biological cofactors that play crucial roles in almost all of fundamental life processes, including respiration, photosynthesis, nitrogen fixation, DNA replication and repair. "Everyone has trillions of iron-sulfur clusters associated with enzymes and proteins in their bodies," Johnson said. "The problem is that they readily degrade in the presence of oxygen and other species that are associated with oxidative stress, leading to loss of protein function."
The research conducted at UGA and UEA focused on FNR, which senses the presence of oxygen in the environment and "switches" off and on specific genes in pathogens, such as E. coli, when there is no oxygen present-conditions often found in the human intestinal tract. Oxygen is sensed by FNR via its iron-sulfur cluster-that undergoes conversion from one form to another, smaller one, thereby causing the protein to change shape-the "switch"-and leading to the turning off of genes associated with growth without oxygen.
"E. coli can decide what lifestyle to live, with or without oxygen," said Johnson. "We can't decide to change our need for oxygen, but understanding the mechanisms for reassembly and repair of iron-sulfur clusters in response to oxidative stress is crucial for understanding a host of human diseases as well as the aging process."
By revealing the structure of the oxygen-damaged cluster in FNR and showing that it can be readily repaired by the addition of iron, this research has discovered a major mechanism for the repair of iron-sulfur clusters. Moreover, preliminary results on other iron-sulfur cluster containing enzymes suggest that this type of iron-sulfur cluster oxygen-damage and repair mechanism is widespread in biology.
Bo Zhang, the lead author on paper said that the iron-sulfur cluster switching mechanism in response to oxygen is smart. "They don't panic-they calmly keep their extra sulfurs and wait to be repaired," said Zhang. She said that any medical applications of the research could take 10 to 20 years for development. The next step is to discover how the repair process works in the cell. Johnson and Zhang are currently working on in vitro models to mimic this biological repair process.
Research reported in this publication was supported by the National Institute of General Medical Sciences at the National Institutes of Health under award number GM62524.
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The above story is reprinted from materials provided by University of Georgia. The original article was written by April Reese Sorrow.
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Journal Reference:
- B. Zhang, J. C. Crack, S. Subramanian, J. Green, A. J. Thomson, N. E. Le Brun, M. K. Johnson. Reversible cycling between cysteine persulfide-ligated [2Fe-2S] and cysteine-ligated [4Fe-4S] clusters in the FNR regulatory protein. Proceedings of the National Academy of Sciences, 2012; DOI: 10.1073/pnas.1208787109
Note: If no author is given, the source is cited instead.
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