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- Published online September 12, 2019.
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Copyright © 2019 by The American Society for Pharmacology and Experimental Therapeutics
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- Address correspondence to:
Dr. Henry A. Dunn, The Scripps Research Institute, 130 Scripps Way, Jupiter, FL 33458. E-mail: hdunn{at}scripps.edu; or - Dr. Cesare Orlandi, The Scripps Research Institute, 130 Scripps Way, Jupiter, FL 33458. E-mail: corlandi{at}scripps.edu; or
- Dr. Kirill A. Martemyanov, The Scripps Research Institute, 130 Scripps Way, Jupiter, FL 33458. E-mail: kirill{at}scripps.edu.
- Eric L. Barker, ASSOCIATE EDITOR
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- Article
- Visual Overview
- Abstract
- I. The Emerging Extracellular Dimension of G Protein–Coupled Receptor Modulation
- II. Group III Metabotropic Glutamate Receptors Are Classic Neurotransmitter Receptors Subject to Transsynaptic Control by Endogenous Allosteric Modulators
- III. Alternative Splicing Defines the Extracellular Interactome of γ-Aminobutyric Acid Receptors
- IV. Multimodal Assemblies Involving Adhesion G Protein–Coupled Receptor Subfamily Ls (Latrophilins) Modulate Axonal Attraction, Repulsion, and Synapse Formation
- V. Direct Interaction of Adhesion G Protein–Coupled Receptor Subfamily G1/6 (G Protein–Coupled Receptor 56/126) with Extracellular Matrix Proteins Regulates Adhesion G Protein–Coupled Receptor Activation Mechanisms
- VI. Bidirectional Transsynaptic Coordination of Signaling Involving Complexes Composed of Adhesion G Protein–Coupled Receptor B1-3 (Brain-Specific Angiogenesis Inhibitor 1-3)
- VII. Assembly of Transsynaptic Complexes with Orphan G Protein–Coupled Receptor 158/179 Facilitates Bidirectional Scaffolding of Intracellular Signaling Molecules
- VIII. Concluding Remarks
- Acknowledgments
- Authorship Contributions
- Footnotes
- Abbreviations
- References
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