研究目的
Investigating the interaction of folic acid functionalized gold nanoparticles and gold-shelled Fe3O4 nanoparticles with microtubule and microtubule associated protein tau to introduce intracellular targets and provide a holistic view about the mechanism of action of gold nanoparticles used in photothermal therapy.
研究成果
Gold nanoparticles interact with tubulin and tau proteins via hydrophobic forces, leading to conformational changes and stabilization of microtubules, which may explain the apoptosis observed in photothermal therapy. This suggests microtubule network as a key target for enhancing cancer treatment efficacy.
研究不足
The study is in vitro and may not fully represent in vivo conditions; specific cell culture or animal model validations are not included. The nanoparticles' effects on other cellular components are not explored.
1:Experimental Design and Method Selection:
The study used spectroscopic methods including fluorescence spectroscopy, circular dichroism (CD), and UV/Vis spectrophotometry to investigate interactions and effects on polymerization.
2:Sample Selection and Data Sources:
Tubulin was purified from sheep brain, and tau protein was expressed and purified from E. coli. Gold nanoparticles (FA-AuNPs and AuFeNPs, 20nm diameter) were purchased.
3:List of Experimental Equipment and Materials:
Equipment includes fluorescence spectrometer, CD spectrometer, UV/Vis spectrophotometer (Carry-100 with thermal controller), and materials include gold nanoparticles, tubulin, tau, ANS, GTP, buffers.
4:Experimental Procedures and Operational Workflow:
Fluorescence studies involved titrating nanoparticles into protein solutions and recording emission spectra. ANS experiments measured hydrophobicity changes. CD spectroscopy recorded structural changes. Tubulin polymerization was monitored kinetically at 350 nm and 37°C.
5:Data Analysis Methods:
Data were analyzed using Stern-Volmer plots, modified Stern-Volmer equations, FRET analysis, and CDNN software for secondary structure deconvolution.
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