#GPCRs
Just read a paper from the David Baker group and collaborators designing small protein agonists and antagonists for multiple GPCRs--mind blowing
pubmed.ncbi.nlm.nih.gov/42168559/
November 5, 2026 at 1:44 AM
Mapping the sequence determinants of constitutive activity in GPCRs https://www.biorxiv.org/content/10.64898/2026.10.30.762644v1
November 3, 2026 at 10:45 PM
Removing AT1R receptors cut signaling by up to 90% in engineered cells, versus about 30% with existing blockers—a different approach to a major drug-target family. doi.org/hcq6tt
A much-needed new way to inactivate GPCRs, the most common drug targets
About one-third of all drugs approved by the U.S. Food and Drug Administration target G protein-coupled receptors (GPCRs), a family of more than 800 cell-surface receptors that regulate a wide range of vital functions, including blood pressure, heart rate and immunity.
medicalxpress.com
November 4, 2026 at 2:41 PM
Mapping the sequence determinants of constitutive activity in GPCRs https://www.biorxiv.org/content/10.64898/2026.10.30.762644v1
November 3, 2026 at 10:45 PM
CRV Science Wiki
🧬 Opsin — Animal (Type II) opsins are 7-transmembrane GPCRs covalently bound to 11-cis-retinal that diverged in Urbilateria into hyperpolarizing ciliary (c-opsin / transducin / PDE6 / CNG) and depolarizing rhabdomeric (r-opsin / Gq / PLCβ / TRP)…

https://crvscience.com/wiki/opsin
CRV Science Wiki 🧬 Opsin — Animal (Type II) opsins are 7-transmembrane GPCRs covalently bound to 11-cis-retinal that diverged in Urbilateria into hyperpolarizing ciliary (c-opsin / transducin / PDE6 / CNG) and depolarizing rhabdomeric (r-opsin / Gq / PLCβ / TRP) photoreceptor cell lineages.
crvscience.com
November 5, 2026 at 7:22 AM
Feigin is not normally right (Untoasted bagels, Buffalo, Bills, GPCRs, etc.) But here he speaks the truth.
You can read a million papers. You can train all the AIs. At some point you need to pick up a fucking pipette.
October 29, 2026 at 5:24 PM
CRV Science Wiki
🧬 Opioid Receptor and Analgesic Pharmacology — Opioid receptors constitute a subfamily of four seven-transmembrane Class A (rhodopsin-like) G-protein-coupled receptors (GPCRs)—the mu (μ / MOR), delta (δ / DOR), kappa (κ /…

https://crvscience.com/wiki/opioid-receptor-and-analgesic
CRV Science Wiki 🧬 Opioid Receptor and Analgesic Pharmacology — Opioid receptors constitute a subfamily of four seven-transmembrane Class A (rhodopsin-like) G-protein-coupled receptors (GPCRs)—the mu (μ / MOR), delta (δ / DOR), kappa (κ / KOR), and nociceptin/orphanin FQ (NOP / ORL1) receptors—th…
crvscience.com
November 3, 2026 at 6:09 AM
Microbial products trigger chemosensory dialogues via GPCRs

Libraries of gut metabolites+GPCR-seq reveal how gut senses environmental chemicals. ID microbial products activating specific receptors, including those triggering serotonin or linking to IBD
www.cell.com/cell-host-mi...
Microbial products trigger chemosensory dialogues through intestinal G protein-coupled receptors
Kadoki et al. developed GPCR-seq, a high-throughput platform to identify how the gut senses environmental chemicals. They discovered gut microbial products that activate intestinal receptors, triggeri...
www.cell.com
October 30, 2026 at 5:00 PM
aren't GPCRs used for migraines?
October 26, 2026 at 8:47 PM
mechanoLight: A genetically encoded fluorescent biosensor for visualizing 5-HT2AR mechanotransduction in live cells
www.pnas.org/doi/abs/10.1...
mechanoLight: A genetically encoded fluorescent biosensor for visualizing 5-HT2AR mechanotransduction in live cells | PNAS
G protein–coupled receptors (GPCRs) are pivotal sensors of the mechanical environment, yet how they sense and transduce physical stimuli into bioch...
www.pnas.org
October 27, 2026 at 7:25 PM
🔬GPCRs are linked to many chronic diseases, acting as a central regulator of health. Therapies that rebalance GPCR signaling across tissues could enable a broader therapeutic effect that could potentially extend healthspan and prevent age-related diseases.

#MolecularBiology #AgingResearch #SciComm
October 26, 2026 at 3:02 PM
Modulating GPCR signaling could help delay multiple age-related diseases
Researchers have outlined a bold plan for slowing aging by targeting one of the body's most important cellular communication systems. In a new paper published today in Frontiers in Science, scientists describe how novel therapies that modulate GPCR signaling could one day help delay multiple age-related diseases at once-potentially extending healthy years of life. GPCRs are widespread throughout the body and regulate many essential biological processes. Age-related changes in GPCR signaling are linked to multiple hallmarks of aging and many major chronic diseases. The authors propose that therapies designed to rebalance GPCR signaling across tissues could therefore help counter some of the key biological processes that drive aging and age-related disease. What's most exciting about this network-level GPCR approach is its ability to influence many of the biological systems that change with age at the same time." Prof. Stuart Maudsley, Senior Author, H. Lee Moffitt Cancer Center, Florida This network-level approach-targeting multiple GPCR pathways across the body rather than a single receptor or disease-could give rise to highly personalized treatments based on individual aging biomarkers, the researchers say, as well as advanced strategies that modulate GPCR signaling across different tissues and pathways. These interventions could also complement other emerging longevity...
www.news-medical.net
October 24, 2026 at 10:44 AM
GPCR Signaling Modulation Offers Potential for Delaying Multiple Age-Related Diseases

🤖 IA: It's not clickbait ✅
👥 Users: It's not clickbait ✅

#aging #disease #therapy

👇👇👇
GPCR Signaling Modulation Offers Potential for Delaying Multiple Age-Related Diseases
Researchers have proposed a novel approach to slowing aging by targeting G protein-coupled receptors (GPCRs), which are widespread throughout the body and regulate essential biological processes. In a paper published in Frontiers in Science, scientists outline how therapies that modulate GPCR signaling could potentially delay multiple age-related diseases simultaneously, extending healthy years of life. GPCRs play a critical role in regulating hormones, metabolism, brain function, immune responses, and other key systems. Age-related changes in GPCR signaling are linked to several hallmarks of aging, including chronic inflammation, reduced cellular energy production, genomic dysregulation, and impaired cellular communication. The authors suggest that rebalancing GPCR signaling across tissues could counteract these aging processes. This network-level approach, targeting multiple GPCR pathways rather than a single receptor or disease, could lead to highly personalized treatments based on individual aging biomarkers. Such therapies could complement other longevity strategies like metabolic therapies, regenerative medicine, and anti-inflammatory treatments. The researchers emphasize that GPCRs are highly 'druggable' and could provide a powerful platform for developing therapies aimed at extending healthspan and preventing age-related diseases. Advances in artificial intelligence, systems biology, and precision medicine are enabling new GPCR-based therapies that target the biological mechanisms underlying aging. Co-authors highlighted the potential for personalization, noting that individual biological complexity can be leveraged to develop tailored treatments by identifying drivers of processes at the systems level. They also mentioned that a triad of human experts, glass-box AI systems, and experimental validation could facilitate more precise interventions designed around prevention and long-term health maintenance. The international team believes this approach could transform how we prevent and treat age-related diseases, potentially making conditions like Alzheimer's, diabetes, and cardiovascular diseases preventable or treatable rather than inevitable. The research, led by Prof. Stuart Maudsley from H. Lee Moffitt Cancer Center, represents a promising new direction in longevity science.
en.killbait.com
October 23, 2026 at 6:30 AM
一個54量子位的IQM處理器配合GPU模擬了ADGRG1蛋白質在其原生膜中的自體蛋白水解,消解了計算分歧並降低了能量障礙。這一突破可能使GPCRs的治療靶向成為可能——GPCRs與侵襲性癌症以及...

#量子模擬 #藥物發現 #新聞
混合量子-經典模擬模型利用54量子位IQM處理器研究ADGRG1蛋白質自體蛋白水解
iq.fp2.dev
October 21, 2026 at 10:37 PM
Ein 54-Qubit-IQM-Prozessor, gekoppelt mit GPUs, simulierte ADGRG1-Protein-Autoproteolysis in ihrer nativen Membran, löste rechnerische Unstimmigkeiten und senkte Energiebarrieren. Dieser Durchbruch könnte eine therapeutische Ausrichtung auf GPCRs—verwickelt in aggressive Krebs...
Hybrid Quanten-klassische Simulation modelliert ADGRG1-Protein-Autoproteolysis mit 54-Qubit-IQM-Prozessor
quantumzeitgeist.com
October 21, 2026 at 10:39 PM
A 54-qubit IQM processor coupled with GPUs simulated ADGRG1 protein autoproteolysis in its native membrane, resolving computational disagreements and lowering energy barriers. This breakthrough could enable therapeutic targeting of GPCRs—implicated in aggressive cancers and br...
Hybrid Quantum-Classical Simulation Models ADGRG1 Protein Autoproteolysis with 54-Qubit IQM Processor
quantumzeitgeist.com
October 21, 2026 at 10:37 PM
מעבד IQM בן 54 קיוביטים המצומד ל-GPUs שביצע סימולציה של אוטופרוטאוליזה של חלבון ADGRG1 בממברנתו הטבעית, מה שפתר חילוקי דעות חישוביים והנמיך מחסומי אנרגיה. פריצת דרך זו יכולה לאפשר מטרה טיפולית של GPCRs—שמעורבים בסרטנים אגרסיביים ו-br...

#סימולציהקוונטית #גילויתרופות #חדשות
מודלי סימולציה היברידיים קוונטיים-קלאסיים של אוטופרוטאוליזה של חלבון ADGRG1 עם מעבד IQM בן 54 קיוביטים
quantumzeitgeist.com
October 21, 2026 at 10:40 PM
GPUs와 결합된 54-큐빗 IQM 프로세서가 ADGRG1 단백질의 자연적 막 환경에서의 자가분해를 시뮬레이션했으며, 계산상의 불일치를 해결하고 에너지 장벽을 낮췄습니다. 이 획기적인 성과는 공격성 암 및 기타 질병과 관련된 GPCRs의 치료적 표적화를 가능하게 할 수 있습니다...

#양자시뮬레이션 #신약개발 #뉴스
하이브리드 양자-고전 시뮬레이션이 54-큐빗 IQM 프로세서로 ADGRG1 단백질 자가분해를 모델링합니다
quantumzeitgeist.com
October 21, 2026 at 10:38 PM
One of these positions will focus on ion channels and another on other types of receptors with emphasis on GPCRs but we are also open to other areas. Experience in neuroscience and pharmacology is a must, and some experience in drug development is strong preferred. Positions are open rank.
October 21, 2026 at 6:23 PM
Um processador IQM de 54 qubits acoplado com GPUs simulou a autoproteólise da proteína ADGRG1 em sua membrana nativa, resolvendo desacordos computacionais e reduzindo barreiras de energia. Este avanço poderia permitir o direcionamento terapêutico de GPCRs—implicados em câncere...
Modelos de Simulação Híbrida Quântico-Clássica Modelam Autoproteólise da Proteína ADGRG1 com Processador IQM de 54 Qubits
quantumzeitgeist.com
October 21, 2026 at 10:41 PM
استخدم معالج IQM بـ 54 كيوبت مقترنًا بوحدات معالجة الرسومات (GPUs) محاكاة تحلل بروتين ADGRG1 الذاتي في غشائه الطبيعي، مما حل الاختلافات الحسابية وخفّض حواجز الطاقة. يمكن لهذا الاختراق أن يمكّن الاستهداف العلاجي للمستقبلات المقترنة بالبروتينات الناقلة (GPCRs)—المرتبطة بالسرطانا...
نماذج محاكاة هجينة كمومية-كلاسيكية لدراسة تحلل بروتين ADGRG1 الذاتي باستخدام معالج IQM بـ 54 كيوبت
iq.fp2.dev
October 21, 2026 at 10:40 PM