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Combining ligand design and photo-ligation to provide optimal quantum dot-bioconjugates for sensing and imaging

机译:结合配体设计和光连接,为传感和成像提供最佳量子点-生物共轭物

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We describe the design and synthesis of two metal-coordinating zwitterion ligands to promote the transfer of hydrophobic QDs to buffer media over broad range of conditions. The ligands are prepared by appending either one or two lipoic acid anchoring groups onto a zwitterion, LA-TEG_(200)-ZW and bis(LA)-ZW. Combining these ligands with a photochemical reduction of the lipoic acid group in the presence of UV irradiation, provides an easy to implement method to transfer luminescent QDs to buffer media, while preserving their optical and spectroscopic properties intact. The resulting zwitterion-QDs have very thin capping shell, which allows their self-assembly with full size proteins via metal-to-histidine coordination. These conjugates have great potential for use in various bio-motivated applications.
机译:我们描述了两种金属配位的两性离子配体的设计和合成,以促进疏水QD在宽范围的条件下转移至缓冲介质。通过将一个或两个硫辛酸锚定基团附加到两性离子LA-TEG_(200)-ZW和bis(LA)-ZW上来制备配体。在紫外线照射下将这些配体与硫辛酸基团的光化学还原结合在一起,提供了一种易于实施的方法,可将发光QD转移到缓冲介质中,同时保持其光学和光谱特性不变。生成的两性离子QD具有非常薄的封盖壳,可通过金属与组氨酸的配位使它们与完整蛋白自组装。这些结合物在各种生物动力应用中具有巨大的潜力。

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