Structures of rhodopsin in complex with G-protein-coupled receptor kinase 1
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G-protein-coupled receptor (GPCR) kinases (GRKs) selectively phosphorylate activated GPCRs, thereby priming them for desensitization 1. Although it is unclear how GRKs recognize these receptors 2-4, a conserved region at the GRK N terminus is essential for this process 5-8. Here we report a series of cryo-electron microscopy single-particle reconstructions of light-activated rhodopsin (Rho*) bound to rhodopsin kinase (GRK1), wherein the N terminus of GRK1 forms a helix that docks into the open cytoplasmic cleft of Rho*. The helix also packs against the GRK1 kinase domain and stabilizes it in an active configuration. The complex is further stabilized by electrostatic interactions between basic residues that are conserved in most GPCRs and acidic residues that are conserved in GRKs. We did not observe any density for the regulator of G-protein signalling homology domain of GRK1 or the C terminus of rhodopsin. Crosslinking with mass spectrometry analysis confirmed these results and revealed dynamic behaviour in receptor-bound GRK1 that would allow the phosphorylation of multiple sites in the receptor tail. We have identified GRK1 residues whose mutation augments kinase activity and crosslinking with Rho*, as well as residues that are involved in activation by acidic phospholipids. From these data, we present a general model for how a small family of protein kinases can recognize and be activated by hundreds of different GPCRs.
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Suppressing quantum errors by scaling a surface code logical qubit
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Long-Distance Transmon Coupler with cz-Gate Fidelity above 99.8 %
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Synchronous detection of cosmic rays and correlated errors in superconducting qubit arrays
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GRK2 kinases in the primary cilium initiate SMOOTHENED-PKA signaling in the Hedgehog cascade
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ACKR3–arrestin2/3 complexes reveal molecular consequences of GRK-dependent barcodingPreprint
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Self-citationMechanism of Activation of the Visual Receptor Rhodopsin
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A randomized benchmarking suite for mid-circuit measurements
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Comprehensive insights in GRK4 and hypertension: From mechanisms to potential therapeutics
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Unraveling the Functional Significance of Unstructured Regions in G Protein-Coupled Receptors
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Structural Basis of Arrestin Selectivity for Active Phosphorylated G Protein-Coupled Receptors
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- Authors
- Chen, Q., Plasencia, M., Li, Z., Mukherjee, S., Patra, D., Chen, C.-L., Klose, T., Yao, X.-Q., Kossiakoff, A. A., Chang, L., Andrews, P. C., & Tesmer, J. J. G.
- Affiliations
- Purdue University West Lafayette (US)
- University of Michigan (US)
- University of Chicago (US)
- Georgia State University (US)
- Corresponding author
- Tesmer, John J. G.
- ORCID
- Venue
- Nature
- Published
- 2021-07-14
- Volume
- 595
- Issue
- 7868
- Pages
- 600-605
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC8607881
- OpenAlex
- W3181632501
- Cited by
- 152
- References
- 96
- Citations by year
- 2026: 25 · 2025: 23 · 2024: 33 · 2023: 28 · 2022: 32 · 2021: 11
- FWCI
- 8.15
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- DigitalCommons@UNO (submittedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- IUScholarWorks (Indiana University) (submittedVersion)
- Funders
- National Science Foundation (1517617)
- American Heart Association (19POST34450193)
- Walther Cancer Foundation
- Purdue University
- National Institutes of Health
- National Heart, Lung, and Blood Institute (R01HL122416, R01HL071818)
- National Cancer Institute (R01CA221289, R01CA254402)
- National Institute of General Medical Sciences (R01GM095832, R01GM105942, R01GM105920, R01GM109896, R01GM117372)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Photoreceptor and optogenetics research
- Keywords
- rhodopsin, GRK1, GPCR desensitization, receptor phosphorylation, electrostatic interactions, anionic phospholipids
- MeSH terms
- Amino Acid Sequence, Animals, Binding Sites, Cattle, Rhodopsin, Signal Transduction, Protein Structure, Tertiary, Cryoelectron Microscopy, G-Protein-Coupled Receptor Kinase 1
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