F. Vivaldi , F. Torrini , F. Spiaggia , F. Di Francesco , M. Minunni
{"title":"Exploring affinity receptors in bioanalysis: from natural binders to biomimetics","authors":"F. Vivaldi , F. Torrini , F. Spiaggia , F. Di Francesco , M. Minunni","doi":"10.1016/j.snr.2025.100359","DOIUrl":null,"url":null,"abstract":"<div><div>Affinity receptors have played a pivotal role in advancing bioanalysis, primarily for diagnostic and therapeutic purposes, thanks to their high selectivity toward target molecules, which enables their use in complex biofluids. While antibodies remain the gold standard, ongoing research has explored alternative receptors with improved stability, reduced size, and enhanced performance in bioanalytical and clinical applications. This works traces the evolution of affinity receptors from classical antibodies to emerging biomimetic and synthetic alternatives, including affibodies, nanobodies, aptamers, and molecularly imprinted polymers (MIPs). We highlight their molecular features, advantages, and limitations, emphasizing their use as part of the molecular toolbox for bioanalytical assay development and biosensing. Overall, the continuous diversification of affinity binders reflects the dynamic nature of this field, where the optimal receptor remains context dependent. For this reason, the research into new binders to complement or eventually replace antibodies that, for the moment, remain the choice for high-throughput applications, is still ongoing.</div></div>","PeriodicalId":426,"journal":{"name":"Sensors and Actuators Reports","volume":"10 ","pages":"Article 100359"},"PeriodicalIF":6.5000,"publicationDate":"2025-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sensors and Actuators Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666053925000773","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Affinity receptors have played a pivotal role in advancing bioanalysis, primarily for diagnostic and therapeutic purposes, thanks to their high selectivity toward target molecules, which enables their use in complex biofluids. While antibodies remain the gold standard, ongoing research has explored alternative receptors with improved stability, reduced size, and enhanced performance in bioanalytical and clinical applications. This works traces the evolution of affinity receptors from classical antibodies to emerging biomimetic and synthetic alternatives, including affibodies, nanobodies, aptamers, and molecularly imprinted polymers (MIPs). We highlight their molecular features, advantages, and limitations, emphasizing their use as part of the molecular toolbox for bioanalytical assay development and biosensing. Overall, the continuous diversification of affinity binders reflects the dynamic nature of this field, where the optimal receptor remains context dependent. For this reason, the research into new binders to complement or eventually replace antibodies that, for the moment, remain the choice for high-throughput applications, is still ongoing.
期刊介绍:
Sensors and Actuators Reports is a peer-reviewed open access journal launched out from the Sensors and Actuators journal family. Sensors and Actuators Reports is dedicated to publishing new and original works in the field of all type of sensors and actuators, including bio-, chemical-, physical-, and nano- sensors and actuators, which demonstrates significant progress beyond the current state of the art. The journal regularly publishes original research papers, reviews, and short communications.
For research papers and short communications, the journal aims to publish the new and original work supported by experimental results and as such purely theoretical works are not accepted.