Polydiacetylene liposomes with phenylboronic acid tags: a fluorescence turn-on sensor for sialic acid detection and cell-surface glycan imaging

• Published in: Nanoscale 2018, Vol.10 (9), p.4570-4578
• Main Authors: Wang, Dong-En, Yan, Jiahang, Jiang, Jingjing, Liu, Xiang, Tian, Chang, Xu, Juan, Yuan, Mao-Sen, Han, Xiang, Wang, Jinyi
• Format: Article
• Language: English
• Subjects: Acids; Aqueous solutions; Biological activity; Biological effects; Boronic Acids - chemistry; Cell membranes; Cells (biology); Fluorescence; Glycan; Humans; Imaging; Liposomes; Liposomes - chemistry; MCF-7 Cells; Membranes; Molecular conformation; Monomers; N-Acetylneuraminic Acid - analysis; Polyacetylene Polymer - chemistry; Polydiacetylenes; Polysaccharides - analysis; Restoration; Sensors; Signaling
• ISSN: 2040-3364; 2040-3372
• DOI: 10.1039/c7nr08557e

Sialic acid (SA) located at the terminal end of glycans on cell membranes has been shown to play an important yet distinctive role in various biological and pathological processes. Effective methods for the facile, sensitive and in situ analysis of SA on living cell surfaces are of great significance in terms of clinical diagnostics and therapeutics. Here, a new polydiacetylene (PDA) liposome-based sensor system bearing phenylboronic acid (PBA) and 1,8-naphthalimide derived fluorophore moieties was developed as a fluorescence turn-on sensor for the detection of free SA in aqueous solution and the in situ imaging of SA-terminated glycans on living cell surfaces. In the sensor system, three diacetylene monomers, PCDA-pBA, PCDA-Nap and PCDA-EA, were designed and synthesized to construct the composite PDA liposome sensor. The monomer PCDA-pBA modified with PBA molecules was employed as a receptor for SA recognition, while the monomer PCDA-Nap containing a 1,8-naphthalimide derivative fluorophore was used for fluorescence signaling. When the composite PDA liposomes were formed, the energy transfer between the fluorophore and the conjugated backbone could directly quench the fluorescence of the fluorophore. In the presence of additional SA or SA abundant cells, the strong binding of SA with PBA moieties disturbed the pendent side chain conformation, resulting in the fluorescence restoration of the fluorophore. The proposed methods realized the fluorescence turn-on detection of free SA in aqueous solution and the in situ imaging of SA on living MCF-7 cell surfaces. This work provides a new potential tool for simple and selective analysis of SA on living cell membranes.