{"title":"用于亲和增强生物检测的生物启发DNA框架编程异交。","authors":"Shuai Yang, Chenghao Xi, Xiaolei Zuo, Min Li","doi":"10.1002/smtd.202500822","DOIUrl":null,"url":null,"abstract":"<p><p>Natural polyreactive antibodies achieve enhanced avidity through heterogeneous ligand binding. However, engineering synthetic heteroligation systems with precise control over recognition motif orientation and distance remains challenging. Here, a DNA framework-based strategy is presented to program heterotypic binding by spatially organizing bivalent aptamers targeting platelet-derived growth factor-BB (PDGF-BB). By systematically tuning the distance between heterotypic recognition motifs, programmable modulation of binding affinity is demonstrated. The resulting heteroligation exhibits rapid binding kinetics, high specificity, and ultrasensitive detection of PDGF-BB, with a limit of detection reaching 0.5 pM. This approach provides a versatile platform for designing multivalent interactions, with potential applications in disease diagnostics and immunotherapy for cancer, viral infections, and allergic disorders.</p>","PeriodicalId":229,"journal":{"name":"Small Methods","volume":" ","pages":"e00822"},"PeriodicalIF":9.1000,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bioinspired DNA Framework-Programmed Heteroligation for Affinity-Enhanced Biodetection.\",\"authors\":\"Shuai Yang, Chenghao Xi, Xiaolei Zuo, Min Li\",\"doi\":\"10.1002/smtd.202500822\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Natural polyreactive antibodies achieve enhanced avidity through heterogeneous ligand binding. However, engineering synthetic heteroligation systems with precise control over recognition motif orientation and distance remains challenging. Here, a DNA framework-based strategy is presented to program heterotypic binding by spatially organizing bivalent aptamers targeting platelet-derived growth factor-BB (PDGF-BB). By systematically tuning the distance between heterotypic recognition motifs, programmable modulation of binding affinity is demonstrated. The resulting heteroligation exhibits rapid binding kinetics, high specificity, and ultrasensitive detection of PDGF-BB, with a limit of detection reaching 0.5 pM. This approach provides a versatile platform for designing multivalent interactions, with potential applications in disease diagnostics and immunotherapy for cancer, viral infections, and allergic disorders.</p>\",\"PeriodicalId\":229,\"journal\":{\"name\":\"Small Methods\",\"volume\":\" \",\"pages\":\"e00822\"},\"PeriodicalIF\":9.1000,\"publicationDate\":\"2025-09-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Small Methods\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1002/smtd.202500822\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small Methods","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/smtd.202500822","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Bioinspired DNA Framework-Programmed Heteroligation for Affinity-Enhanced Biodetection.
Natural polyreactive antibodies achieve enhanced avidity through heterogeneous ligand binding. However, engineering synthetic heteroligation systems with precise control over recognition motif orientation and distance remains challenging. Here, a DNA framework-based strategy is presented to program heterotypic binding by spatially organizing bivalent aptamers targeting platelet-derived growth factor-BB (PDGF-BB). By systematically tuning the distance between heterotypic recognition motifs, programmable modulation of binding affinity is demonstrated. The resulting heteroligation exhibits rapid binding kinetics, high specificity, and ultrasensitive detection of PDGF-BB, with a limit of detection reaching 0.5 pM. This approach provides a versatile platform for designing multivalent interactions, with potential applications in disease diagnostics and immunotherapy for cancer, viral infections, and allergic disorders.
Small MethodsMaterials Science-General Materials Science
CiteScore
17.40
自引率
1.60%
发文量
347
期刊介绍:
Small Methods is a multidisciplinary journal that publishes groundbreaking research on methods relevant to nano- and microscale research. It welcomes contributions from the fields of materials science, biomedical science, chemistry, and physics, showcasing the latest advancements in experimental techniques.
With a notable 2022 Impact Factor of 12.4 (Journal Citation Reports, Clarivate Analytics, 2023), Small Methods is recognized for its significant impact on the scientific community.
The online ISSN for Small Methods is 2366-9608.