G protein-coupled receptors (GPCRs) are the most abundantly expressed proteins in the human body, regulating diverse physiological processes ranging from pain perception to hormone signaling. Owing to their central roles in health and disease, GPCRs are the targets of a majority of new drugs under development. Despite their importance, discovering drug candidates that bind to GPCRs with high affinity and specificity remains a major challenge, slowing the development of safer therapeutics.
One promising alternative to conventional drugs is the use of DNA aptamers (short, single-stranded DNAs that can fold into unique 3D structures), which are capable of recognizing specific molecular targets. While this holds promise, aptamer development techniques, such as cell-systematic evolution of ligands by exponential enrichment (SELEX), often struggle to produce candidates against complex membrane proteins like GPCRs.
Addressing this challenge, a research team led by Professor Toshihide Tabata from the Faculty of Engineering, University of Toyama, Japan, along with Dr. Mitsushi J. Ikemoto from the Department of Engineering, University of Toyama, and the Institute of Health and Sports Sciences, University of Tsukuba, Japan; Associate Professor Yuji Kamikubo from the Department of Pharmacology, Juntendo University School of Medicine, Japan; and Associate Professor Daisuke Uta from the Faculty of Pharmaceutical Sciences, University of Toyama, developed a new aptamer selection strategy termed extracellular vesicle (EV)-SELEX. The study is published in Communications Biology.
"As neuroscientists, while working on GPCR-mediated synaptic plasticity, we noticed that there are only a limited number of experimental tools to pharmacologically manipulate neuronal GPCRs. This intrigued us to create new and efficient tools for drug development," Tabata says.
Using vesicles to isolate targets
Unlike conventional Cell-SELEX methods, EV-SELEX exploits a natural cellular process in which activated GPCRs are internalized and packaged into EVs. When a ligand binds to a GPCR, the activated receptor, along with the ligand, is internalized into the cell through endocytosis. These receptors are packaged into EVs and then released into the extracellular space.
The researchers could pick up the receptor-bound ligand by collecting the culture medium around the cells. This minimizes the interference of unrelated membrane proteins and enables efficient selection of DNA aptamers that recognize biologically relevant receptor conformations.
An aptamer that activates MOR
Using this approach, the researchers identified Dapt-μR, a DNA aptamer that can bind to the μ-opioid receptor (MOR) with high specificity. Interestingly, the aptamer did not just recognize the receptor; it also activated it. When tested in cultured cells, Dapt-μR inhibited cyclic adenosine monophosphate accumulation, a hallmark of MOR activation. The effect was blocked by the MOR antagonist naloxone, which confirmed that the response was specifically mediated through MOR.
The team further evaluated the biological activity of the aptamer in neuronal and animal models. In neuronal models, Dapt-μR reduced calcium influx, which was consistent with MOR signaling. In mice, Dapt-μR produced an analgesic effect following intrathecal administration. These findings indicate that the DNA aptamers can function as drug-like molecules capable of triggering a pharmacological response comparable to that of established opioid agonists.
Faster selection with broader potential
Furthermore, the researchers compared EV-SELEX with an improved Cell-SELEX protocol and found that the EV-based method enabled the selection of high-affinity, potent aptamers in fewer selection cycles than conventional methods. This improved efficiency suggests that EV-SELEX could markedly reduce the time and effort required to develop therapeutic candidates for GPCRs.
Beyond the development of a promising opioid receptor-targeting aptamer, the study also established EV-SELEX as a versatile platform that could be applied to drug discovery for a wide range of GPCRs involved in neurological disorders, chronic pain, metabolic diseases, cardiovascular conditions and cancer. In addition to the therapeutic applications, the technology could also generate highly selective molecular tools for studying GPCRs.
"Our new technique, EV-SELEX, can complete drug development in a very short time. It may help pharmaceutical companies efficiently develop therapeutic and/or experimental drugs for the most important drug targets, GPCRs. This technological revolution will greatly promote biomedical science," Tabata concludes.
Publication details
Efficient and Specific Selection of High-Affinity DNA Aptamers Targeting µ-Opioid Receptor via Functional Extracellular Vesicles, Communications Biology (2026). DOI: 10.1038/s42003-026-10525-0
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Citation: EV-SELEX speeds GPCR drug discovery by capturing receptor-bound DNA aptamers (2026, July 7) retrieved 14 July 2026 from https://phys.org/news/2026-07-ev-selex-gpcr-drug-discovery.html
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