Brian Kobilka
Key Documents
Contact Information
- Academic Offices
Personal Information Email Tel (650) 723-7069
Professional Overview
Postdoctoral Advisees
Sherwin Abraham, Andrea Aguilar, Yang Du, Daniel Hilger, Rie Nygaard, Thor Thorsen, Cheng Zhang, Yaozhong Zou
Internet Links
Industry Relationships
Stanford is committed to ethical and transparent interactions with our industrial and other commercial partners. It is our policy to disclose payments (exclusive of travel support) from, and/or equity in, companies or other commercial entities to Stanford faculty of $5,000 or more in total value, as well as any equity in a privately held company, when the faculty member also has institutional responsibilities related to his or her interactions with the company. View Full Information
Scientific Focus
Current Research Interests
My laboratory is involved in studying several aspects of adrenergic receptor biology. Adrenergic receptors form the interface between the sympathetic nervous system and the cardiovascular system and play a critical role in the regulation of cardiovascular function. Specific projects include:
1- RECEPTOR STRUCTURE: We are interested in understanding the three dimensional structure of adrenergic receptors and learning about the conformational changes that mediate signal transduction. We are taking several experimental approaches including mutagenesis, biochemical, and biophysical studies.
2-INTRACELLULAR TRAFFICKING OF ADRENERGIC RECEPTORS: The function of receptors can be modulated by changes in receptor structure (phosphorylation) and by changes in subcellular localization. We are using immunocytochemical approaches to study the targeting of receptors to specific subcellular domains and agonist mediated redistribution of receptors. Our goal is to determine the functional significance of differences in targeting and trafficking that we have observed in several adrenergic receptors, and to identify cellular proteins that mediate receptor trafficking.
3-PHYSIOLOGIC RELEVANCE OF ADRENERGIC RECEPTOR SUBTYPE DIVERSITY: Multiple closely related subtypes of adrenergic receptors have been identified through cloning studies. We are using targeted gene modification in mice to study the physiologic role of these closely related subtypes. We have disrupted the genes for five adrenergic receptors (alpha 2a, alpha 2b, alpha 2c, beta 1, and beta2) and are investigating the consequence of these disruptions on neural and cardiovascular physiology.
Publications
- Crystal structure of the β2 adrenergic receptor-Gs protein complex. Nature. 2011; (7366): 549-55
- Structural insights into adrenergic receptor function and pharmacology. Trends Pharmacol Sci. 2011; (4): 213-8
- Structure and function of an irreversible agonist-β(2) adrenoceptor complex. Nature. 2011; (7329): 236-40
- Structure of a nanobody-stabilized active state of the β(2) adrenoceptor. Nature. 2011; (7329): 175-80
- A device for separated and reversible co-culture of cardiomyocytes. Biotechnol Prog. 2010 Jul-Aug; (4): 1164-71
- Ligand-specific regulation of the extracellular surface of a G-protein-coupled receptor. Nature. 2010; (7277): 108-12