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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
来源:
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.
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页数:11
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