Interfacial hydration determines orientational and functional dimorphism of sterol-derived Raman in lipid-coated nanoparticles

被引:12
作者
An, Xingda [1 ,2 ]
Majumder, Ayan [1 ]
McNeely, James [1 ]
Yang, Jialing [1 ,2 ]
Puri, Taranee [1 ]
He, Zhiliang [1 ]
Liang, Taimeng [1 ]
Snyder, John K. [1 ]
Straub, John E. [1 ]
Reinhard, Bjorn M. [1 ,2 ]
机构
[1] Boston Univ, Dept Chem, 590 Commonwealth Ave, Boston, MA 02215 USA
[2] Boston Univ, Photon Ctr, Boston, MA 02215 USA
关键词
lipid-coated nanoparticles; hydrogen bonding; epidermal growth factor; cholesterol; surface enhanced  Raman spectroscopy; CHOLESTEROL HYDROXYL GROUP; SILVER NANOPARTICLES; GOLD NANOPARTICLES; FORCE-FIELD; FLIP-FLOP; SCATTERING; BILAYER; COLOCALIZATION; SPECTROSCOPY; RECEPTORS;
D O I
10.1073/pnas.2105913118
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Lipid-coated noble metal nanoparticles (L-NPs) combine the biomimetic surface properties of a self-assembled lipid membrane with the plasmonic properties of a nanoparticle (NP) core. In this work, we investigate derivatives of cholesterol, which can be found in high concentrations in biological membranes, and other terpenoids, as tunable, synthetic platforms to functionalize L-NPs. Side chains of different length and polarity, with a terminal alkyne group as Raman label, are introduced into cholesterol and betulin frameworks. The synthesized tags are shown to coexist in two conformations in the lipid layer of the L-NPs, identified as "head-out" and "head-in" orientations, whose relative ratio is determined by their interactions with the lipid- water hydrogen-bonding network. The orientational dimorphism of the tags introduces orthogonal functionalities into the NP surface for selective targeting and plasmon-enhanced Raman sensing, which is utilized for the identification and Raman imaging of epidermal growth factor receptor-overexpressing cancer cells.
引用
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页数:11
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