Researchers develop nanoparticles to target disease proteins

Scientists have created innovative nanoparticles designed to destroy harmful proteins linked to dementia and cancer. These particles can access difficult tissues like the brain and precisely eliminate problematic proteins without broad side effects. The technology shows early promise for precision medicine.

A team of researchers has introduced a novel approach using engineered nanoparticles to tackle 'undruggable' proteins that drive diseases such as dementia and brain cancer. Led by Chair Professor in Nanomedicine Bingyang Shi at the University of Technology Sydney, in collaboration with Professor Kam Leong of Columbia University and Professor Meng Zheng of Henan University, the work was detailed in a perspective article published in Nature Nanotechnology.

Abnormal proteins, which can mutate, misfold, or accumulate improperly, disrupt cell functions and cause conditions like cancer and autoimmune disorders. 'Proteins are essential for nearly every function in the body, but when they become mutated, misfolded, overproduced, or build up in the wrong place, they can disrupt normal cell processes and trigger disease,' said Professor Shi. Many of these proteins resist traditional drug treatments due to their shapes or behaviors.

The new technology, called nanoparticle-mediated targeting chimeras (NPTACs), allows these particles to bind to specific disease-related proteins and direct them into the body's natural recycling system for breakdown. 'We have developed an efficient and flexible method to guide disease-causing proteins, whether inside or outside the cell, into the body's natural recycling system, where they can be broken down and removed,' Professor Shi explained. This builds on an original discovery reported in Nature Nanotechnology in October 2024.

Unlike existing targeted protein degradation tools, which face challenges in tissue access and off-target effects, NPTACs offer advantages including degradation of both intra- and extracellular proteins, targeting across the blood-brain barrier, modular adaptability, scalability using FDA-approved materials, and potential for multifunctional use. Preclinical studies have shown encouraging results against proteins like EGFR, which promotes tumor growth, and PD-L1, which helps cancer evade the immune system.

The field of targeted protein degradation is booming, with companies like Arvinas raising over $1 billion and partnering with firms such as Pfizer, Bayer, and Roche. The market is projected to exceed $10 billion by 2030. 'This progress paves the way for applications in oncology, neurology and immunology. It changes how we think about nanoparticles - not only as delivery tools but also as active therapeutic agents,' said Professor Shi. The team holds multiple international patents and is seeking industry partners to advance clinical development and regulatory approval.

The full study appears in Nature Nanotechnology (2026; DOI: 10.1038/s41565-025-02081-1).

Связанные статьи

Scientific illustration depicting healthy and damaged tanycytes in the brain's third ventricle clearing tau protein in Alzheimer’s disease.
Изображение, созданное ИИ

Study links tanycyte damage to reduced tau clearance in Alzheimer’s disease

Сообщено ИИ Изображение, созданное ИИ Проверено фактами

Researchers report that tanycytes—specialized cells lining the brain’s third ventricle—can help move tau protein from cerebrospinal fluid into the bloodstream, and that signs of tanycyte disruption in Alzheimer’s patient tissue may be associated with impaired tau removal. The findings, published March 5 in Cell Press Blue, are based on animal and cell experiments and analyses of human brain samples.

A team of researchers led by Professor Yan-Jiang Wang has published a review arguing that Alzheimer's disease requires integrated treatments targeting multiple factors, not single causes. New drugs like lecanemab and donanemab offer modest benefits by slowing decline, but fall short of reversal. The paper, in Science China Life Sciences, emphasizes genetics, aging, and systemic health alongside amyloid-beta and tau proteins.

Сообщено ИИ

Researchers at UCLA Health and UC San Francisco have identified a natural defense mechanism in brain cells that helps remove toxic tau protein, potentially explaining why some neurons resist Alzheimer's damage better than others. The study, published in Cell, used CRISPR screening on lab-grown human neurons to uncover this system. Findings suggest new therapeutic avenues for neurodegenerative diseases.

Researchers in Australia have found that a mysterious FDA-approved drug, called compound X, removes toxic alpha-synuclein proteins from the brains of mice with Parkinson's-like symptoms. The treatment improved the animals' balance and mobility by enhancing the brain's glymphatic waste disposal system. The findings were presented at a symposium in the UK.

Сообщено ИИ Проверено фактами

Researchers at the University of California, Irvine report that a machine-learning system called SIGNET can infer cause-and-effect links between genes in human brain tissue, revealing extensive rewiring of gene regulation—especially in excitatory neurons—in Alzheimer’s disease.

Этот сайт использует куки

Мы используем куки для анализа, чтобы улучшить наш сайт. Прочитайте нашу политику конфиденциальности для дополнительной информации.
Отклонить