How to Build Plasmon-Driven Molecular Jackhammers that Disassemble Cell Membranes and Cytoskeletons in Cancer.
Ciceron Ayala-OrozcoGang LiBowen LiVardan VardanyanAnatoly B KolomeiskyJames M TourPublished in: Advanced materials (Deerfield Beach, Fla.) (2024)
Plasmon-driven molecular machines with ultrafast motion at the femtosecond scale are effective for the treatment of cancer and other diseases. It is recently shown that cyanine dyes act as molecular jackhammers (MJH) through vibronic (vibrational and electronic mode coupling) driven activation that causes the molecule to stretch longitudinally and axially through concerted whole molecule vibrations. However, the theoretical and experimental underpinnings of these plasmon-driven motions in molecules are difficult to assess. Here the use of near-infrared (NIR) light-activated plasmons in a broad array of MJH that mechanically disassemble membranes and cytoskeletons in human melanoma A375 cells is described. The characteristics of plasmon-driven molecular mechanical disassembly of supramolecular biological structures are observed and recorded using real-time fluorescence confocal microscopy. Molecular plasmon resonances in MJH are quantified through a new experimental plasmonicity index method. This is done through the measurement of the UV-vis-NIR spectra in various solvents, and quantification of the optical response as a function of the solvent polarity. Structure-activity relationships are used to optimize the synthesis of plasmon-driven MJH, applying them to eradicate human melanoma A375 cells at low lethal concentrations of 75 nm and 80 mW cm -2 of 730 nm NIR-light for 10 min.
Keyphrases
- energy transfer
- photodynamic therapy
- induced apoptosis
- endothelial cells
- single molecule
- high resolution
- papillary thyroid
- quantum dots
- fluorescence imaging
- drug release
- high throughput
- induced pluripotent stem cells
- single cell
- squamous cell
- squamous cell carcinoma
- molecular dynamics simulations
- oxidative stress
- bone marrow
- fluorescent probe
- cell proliferation
- endoplasmic reticulum stress
- skin cancer
- basal cell carcinoma