Doctoral Program of Engineering Physics, Faculty of Industrial Technology, Institut Teknologi Bandung, Ganesha 10, Bandung 40132, Indonesia.
Advanced Functional Material Laboratory, Faculty of Industrial Technology, Institut Teknologi Bandung, Jl. Ganesha No. 10, Bandung 41032, Indonesia.
ACS Biomater Sci Eng. 2024 Apr 8;10(4):2041-2061. doi: 10.1021/acsbiomaterials.3c01965. Epub 2024 Mar 25.
In tropical and developing countries, mosquito-borne diseases by flaviviruses pose a serious threat to public health. Early detection is critical for preventing their spread, but conventional methods are time-consuming and require skilled technicians. Biosensors have been developed to address this issue, but cross-reactivity with other flaviviruses remains a challenge. Peptides are essentially biomaterials used in diagnostics that allow virological and serological techniques to identify flavivirus selectively. This biomaterial originated as a small protein consisting of two to 50 amino acid chains. They offer flexibility in chemical modification and can be easily synthesized and applied to living cells in the engineering process. Peptides could potentially be developed as robust, low-cost, sensitive, and selective receptors for detecting flaviviruses. However, modification and selection of the receptor agents are crucial to determine the effectiveness of binding between the targets and the receptors. This paper addresses two potential peptide nucleic acids (PNAs) and affinity peptides that can detect flavivirus from another target-based biosensor as well as the potential peptide behaviors of flaviviruses. The PNAs detect flaviviruses based on the nucleotide base sequence of the target's virological profile via Watson-Crick base pairing, while the affinity peptides sense the epitope or immunological profile of the targets. Recent developments in the functionalization of peptides for flavivirus biosensors are explored in this Review by division into electrochemical, optical, and other detection methods.
在热带和发展中国家,黄病毒引起的蚊媒传染病对公共卫生构成严重威胁。早期检测对于防止其传播至关重要,但传统方法既耗时又需要熟练的技术人员。已经开发出生物传感器来解决这个问题,但与其他黄病毒的交叉反应仍然是一个挑战。肽本质上是用于诊断的生物材料,允许病毒学和血清学技术选择性地识别黄病毒。这种生物材料最初是由两条到 50 条氨基酸链组成的小蛋白质。它们在化学修饰方面具有灵活性,可以在工程过程中轻松合成并应用于活细胞。肽有可能成为检测黄病毒的强大、低成本、敏感和选择性受体。然而,受体试剂的修饰和选择对于确定目标与受体之间的结合有效性至关重要。本文讨论了两种潜在的肽核酸 (PNA) 和亲和肽,它们可以从另一种基于靶标的生物传感器中检测黄病毒,以及黄病毒的潜在肽行为。PNA 通过沃森-克里克碱基配对基于目标病毒学特征的核苷酸碱基序列检测黄病毒,而亲和肽则感知目标的表位或免疫学特征。本文通过分为电化学、光学和其他检测方法,探讨了肽在黄病毒生物传感器中的功能化的最新进展。