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用于材料表面功能化的碲化镉/硫化镉量子点结合肽的筛选与表征

Screening and characterisation of CdTe/CdS quantum dot-binding peptides for material surface functionalisation.

作者信息

Suwatthanarak Thanawat, Tanaka Masayoshi, Minamide Taisuke, Harvie Andrew J, Tamang Abiral, Critchley Kevin, Evans Stephen D, Okochi Mina

机构信息

Department of Chemical Science and Engineering, Tokyo Institute of Technology 2-12-1, O-okayama, Meguro-ku Tokyo 152-8552 Japan

School of Physics and Astronomy, University of Leeds Leeds LS2 9JT UK.

出版信息

RSC Adv. 2020 Feb 26;10(14):8218-8223. doi: 10.1039/d0ra00460j. eCollection 2020 Feb 24.

Abstract

Quantum dots (QDs) are promising nanomaterials due to their unique photophysical properties. For them to be useful in biological applications, the particle surface generally needs to be conjugated to biological molecules, such as antibodies. In this study, we screened CdTe/CdS QD-binding peptides from a phage display library as linkers for simple and bio-friendly QD modification. Among five QD-binding peptide candidates, a series of truncated peptides designed from two high-affinity peptides were subjected to an array-based binding assay with QDs to assess their functional core sequences and characteristics. Linking these isolated, shortened peptides (PWSLNR and SGVYK) with an antibody-binding peptide (NKFRGKYK) created dual-functional peptides that are capable of QD surface functionalisation by antibodies. Consequently, the dual-functional peptides could mediate anti-CD9 antibody functionalisation onto CdTe/CdS QD surface; CD9 protein imaging of cancer cells was also demonstrated. Our proposed peptides offer an effective vehicle for QD surface functionalisation in biological applications.

摘要

量子点(QDs)因其独特的光物理性质而成为很有前景的纳米材料。为了使其在生物应用中发挥作用,粒子表面通常需要与生物分子(如抗体)共轭。在本研究中,我们从噬菌体展示文库中筛选了CdTe/CdS量子点结合肽作为简单且生物友好的量子点修饰连接子。在五个量子点结合肽候选物中,从两个高亲和力肽设计的一系列截短肽与量子点进行了基于阵列的结合测定,以评估其功能核心序列和特性。将这些分离的、缩短的肽(PWSLNR和SGVYK)与抗体结合肽(NKFRGKYK)连接,产生了能够通过抗体对量子点表面进行功能化的双功能肽。因此,双功能肽可以介导抗CD9抗体在CdTe/CdS量子点表面的功能化;还展示了癌细胞的CD9蛋白成像。我们提出的肽为生物应用中的量子点表面功能化提供了一种有效的载体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2c7/9049935/0e3851c13079/d0ra00460j-f1.jpg

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