Nitric oxide (NO) signaling pathways mediate diverse physiological functions, including vasodilation, neurotransmission, myocardial function, and platelet aggregation. Soluble guanylate cyclase (sGC) is the primary receptor of NO. Dysfunctions in the NO-sGC signaling pathway can lead to heart disease, erectile dysfunction, stroke, and hypertension. Understanding the molecular details of NO-induced sGC activation is crucial for developing treatments for these disease states. Mammalian sGC is a multi-domain, heterodimeric hemoprotein. Because full-length sGC has proven intractable to high resolution structure analysis (e.g., X-ray crystallography), the domain architecture and NO-induced conformational changes are poorly understood.
The specific aims of the research proposed herein are focused on illuminating the domain organization and conformational changes of sGC through parallel, complementary protein mapping approaches. Hydrogen-deuterium exchange mass spectrometry (HDX-MS) is a powerful strategy for mapping the solvent exposure of protein surfaces by measuring changes in the rates of amide proton exchange with a deuterated solvent. HDX-MS will be used to map the interaction surfaces of sGC domain truncations. Alanine scanning will be performed to define individual residues that are crucial to sGC inter-domain interactions. To characterize the relative orientations of the sGC domains, hydroxyl radical footprinting will be employed. Hydroxyl radicals generated at a reagent tethered near an inter-domain interaction can cleave polypeptide backbones at proximal residues. These cleavage patterns report on the proximities between surfaces of sGC domains. The results of the HDX-MS, alanine scanning, and hydroxyl radical footprinting will be integrated to develop a model of the domain architecture of full-length sGC. Changes in the sGC domain architecture induced by NO stimulus can then be assessed in full-length sGC. HDX-MS will be used to map NO-induced changes in sGC surface accessibility to develop a model of the conformational changes that control sGC cyclase activity.

Public Health Relevance

Nitric oxide (NO) signaling via soluble guanylate cyclase (sGC) mediates diverse physiological processes crucial to circulatory and neurological function. Disruptions in NO/sGC signaling have been linked to heart disease, stroke, erectile dysfunction, and neurodegeneration. The proposed research aims to illuminate the molecular details of NO- induced sGC activation, a prerequisite for developing treatments for diseases related to NO/sGC dysfunction.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32GM093564-04
Application #
8236975
Study Section
Special Emphasis Panel (ZRG1-F04B-B (20))
Program Officer
Fabian, Miles
Project Start
2010-04-01
Project End
2012-09-30
Budget Start
2012-04-01
Budget End
2012-09-30
Support Year
4
Fiscal Year
2012
Total Cost
$26,971
Indirect Cost
Name
Scripps Research Institute
Department
Type
DUNS #
781613492
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Campbell, Melody G; Underbakke, Eric S; Potter, Clinton S et al. (2014) Single-particle EM reveals the higher-order domain architecture of soluble guanylate cyclase. Proc Natl Acad Sci U S A 111:2960-5
Underbakke, Eric S; Iavarone, Anthony T; Chalmers, Michael J et al. (2014) Nitric oxide-induced conformational changes in soluble guanylate cyclase. Structure 22:602-11
Underbakke, Eric S; Iavarone, Anthony T; Marletta, Michael A (2013) Higher-order interactions bridge the nitric oxide receptor and catalytic domains of soluble guanylate cyclase. Proc Natl Acad Sci U S A 110:6777-82
Smith, Brian C; Underbakke, Eric S; Kulp, Daniel W et al. (2013) Nitric oxide synthase domain interfaces regulate electron transfer and calmodulin activation. Proc Natl Acad Sci U S A 110:E3577-86