JBC

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


A more recent version of this article appeared on July 3, 2003
This Article
Right arrow Full Text (Accepted Manuscript)
Right arrow All Versions of this Article:
278/28/25700    most recent
M212309200v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Roman, L. J.
Right arrow Articles by Masters, B. S. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Roman, L. J.
Right arrow Articles by Masters, B. S. S.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Papers In Press, published online ahead of print May 1, 2003
J. Biol. Chem, 10.1074/jbc.M212309200
Submitted on December 3, 2002
Revised on April 7, 2003
Accepted on May 1, 2003

Chimeric enzymes of cytochrome P450 Oxido-reductase and neuronal nitric oxide synthase reductase domain reveal structural and functional differences between them

Linda J. Roman, Jennifer McLain, and Bettie Sue Siler Masters

Biochemistry-7760, University of Texas Health Science Center, San Antonio, TX 78229

Corresponding Author: roman{at}uthscsa.edu

The nitric oxide synthases (NOSs) are comprised of an oxygenase domain and a reductase domain, bisected by a calmodulin (CaM)-binding region. The NOS reductase domains share ~ 60% sequence similarity with the cytochrome P450 oxido-reductase (CYPOR), which transfers electrons to microsomal cytochromes P450. The crystal structure of the nNOS connecting/FAD-binding subdomains reveals that the structure of the nNOS connecting subdomain diverges from that of CYPOR, implying different alignments of the flavins in the two enzymes. We created a series of chimeric enzymes between nNOS and CYPOR in which the FMN-binding and the connecting/FAD-binding subdomains are swapped. A chimera consisting of the nNOS heme domain and FMN-binding subdomain and the CYPOR FAD-binding subdomain catalyzed significantly increased rates of cytochrome c reduction in the absence of CaM and of NO synthesis in its presence. Cytochrome c reduction by this chimera is inhibited by CaM. Other chimeras consisting of the nNOS heme domain, the CYPOR FMN-binding subdomain, and the nNOS FAD-binding subdomain, with or without the tail region, also catalyzed cytochrome c reduction, were not modulated by CaM, and could not transfer electrons into the heme domain. A chimera consisting of the heme domain of nNOS and the reductase domain of CYPOR reduced cytochrome c and ferricyanide at rates 2-fold higher than that of native CYPOR, suggesting that the presence of the heme domain affected electron transfer through the reductase domain. These data demonstrate that the FMN subdomain of CYPOR cannot effectively substitute for that of nNOS, while the FAD subdomains are interchangeable. The differences among these chimeras most likely result from alterations in the alignment of the flavins within each enzyme construct.


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
Mol. Endocrinol.Home page
A. V. Pandey, P. Kempna, G. Hofer, P. E. Mullis, and C. E. Fluck
Modulation of Human CYP19A1 Activity by Mutant NADPH P450 Oxidoreductase
Mol. Endocrinol., October 1, 2007; 21(10): 2579 - 2595.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
S. P. Panda, Y. T. Gao, L. J. Roman, P. Martasek, J. C. Salerno, and B. S. S. Masters
The Role of a Conserved Serine Residue within Hydrogen Bonding Distance of FAD in Redox Properties and the Modulation of Catalysis by Ca2+/Calmodulin of Constitutive Nitric-oxide Synthases
J. Biol. Chem., November 10, 2006; 281(45): 34246 - 34257.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
L. J. Roman and B. S. S. Masters
Electron Transfer by Neuronal Nitric-oxide Synthase Is Regulated by Concerted Interaction of Calmodulin and Two Intrinsic Regulatory Elements
J. Biol. Chem., August 11, 2006; 281(32): 23111 - 23118.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
M. Jachymova, P. Martasek, S. Panda, L. J. Roman, M. Panda, T. M. Shea, Y. Ishimura, J.-J. P. Kim, and B. S. S. Masters
Recruitment of governing elements for electron transfer in the nitric oxide synthase family
PNAS, November 1, 2005; 102(44): 15833 - 15838.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
P.-F. Chen and K. K. Wu
Structural Elements Contribute to the Calcium/Calmodulin Dependence on Enzyme Activation in Human Endothelial Nitric-oxide Synthase
J. Biol. Chem., December 26, 2003; 278(52): 52392 - 52400.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 All ASBMB Journals   Molecular and Cellular Proteomics 
 Journal of Lipid Research   ASBMB Today 
Copyright © 2003 by the American Society for Biochemistry and Molecular Biology.