Elsevier eBooks, Journal Year: 2024, Volume and Issue: unknown, P. 67 - 82
Published: Nov. 29, 2024
Language: Английский
Elsevier eBooks, Journal Year: 2024, Volume and Issue: unknown, P. 67 - 82
Published: Nov. 29, 2024
Language: Английский
Advances in protein chemistry and structural biology, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 1, 2025
Language: Английский
Citations
1Biosensors, Journal Year: 2024, Volume and Issue: 14(3), P. 146 - 146
Published: March 15, 2024
The global challenges posed by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic have underscored critical importance of innovative and efficient control systems for addressing future pandemics. most effective way to is rapidly suppress spread virus through early detection using a rapid, accurate, easy-to-use diagnostic platform. In biosensors that use bioprobes, binding affinity molecular recognition elements (MREs) primary factor determining dynamic range sensing Furthermore, sensitivity relies mainly on bioprobe quality with sufficient functionality. This comprehensive review investigates aptamers nanobodies recently developed as advanced MREs SARS-CoV-2 therapeutic applications. These bioprobes might be integrated into organic bioelectronic materials devices, promising enhanced specificity. offers valuable insights advancing biosensing technologies infectious disease diagnosis treatment new bioprobes.
Language: Английский
Citations
6Molecular Biotechnology, Journal Year: 2024, Volume and Issue: unknown
Published: Sept. 2, 2024
Language: Английский
Citations
6Advanced Science, Journal Year: 2025, Volume and Issue: unknown
Published: March 26, 2025
The lack of targetable antigens poses a significant challenge in developing effective cancer-targeted therapies. Cell surface translocation endoplasmic reticulum (ER) chaperones, such as glucose-regulated protein 78 (GRP78), during malignancy, drug resistance, and ER stress induced by therapies, offers promising pan-cancer target. To target GRP78, nanobody C5, identified from phage library exhibiting high affinity for human mouse is utilized to develop the Pseudomonas exotoxin (PE) immunotoxin C5-PE38. C5-PE38 stress, apoptosis immunogenic cell death targeted cells showed antitumor efficacy against colorectal cancer melanoma models without obvious toxicity. Mechanistically, transcriptome profiling that reshaped tumor immune microenvironment with enhanced innate adaptive response interferon beta. Moreover, C5-PE38-induced could trans-activate STING pathway dendritic macrophages, promoting CD8+ T infiltration. It also sensitizes both primary metastatic melanomas anti-PD1 therapy, partly through activation. Overall, this study unveils feasible GRP78 nanobody-directed therapy strategy single or combinatorial intervention. This work finds stimulates STING-dependent cytosolic DNA release promote immunity, mechanism not previously reported PE38, providing valuable insights its clinical use.
Language: Английский
Citations
0Microchemical Journal, Journal Year: 2025, Volume and Issue: unknown, P. 114083 - 114083
Published: May 1, 2025
Language: Английский
Citations
0Diagnostic and Interventional Imaging, Journal Year: 2024, Volume and Issue: 105(10), P. 400 - 406
Published: May 14, 2024
Language: Английский
Citations
3Biochimica et Biophysica Acta (BBA) - Reviews on Cancer, Journal Year: 2025, Volume and Issue: unknown, P. 189284 - 189284
Published: Feb. 1, 2025
Language: Английский
Citations
0Elsevier eBooks, Journal Year: 2024, Volume and Issue: unknown, P. 67 - 82
Published: Nov. 29, 2024
Language: Английский
Citations
0