2023年第70回応用物理学会春季学術講演会

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一般セッション(ポスター講演)

3 光・フォトニクス » 3.1 光学基礎・光学新領域(旧3.2「材料・機器光学」と統合)

[16a-PA01-1~10] 3.1 光学基礎・光学新領域(旧3.2「材料・機器光学」と統合)

2023年3月16日(木) 09:30 〜 11:30 PA01 (ポスター)

09:30 〜 11:30

[16a-PA01-6] Cooperative Optical Trapping Dynamics of Protein and Polyethylene Glycol Studied by Fluorescence Imaging and Raman Scattering Micro-spectroscopy

〇(M2)Ching-Yang Lin1、Wei-Hsiang Chiu1、Hiroshi Masuhara1 (1.National Yang Ming Chiao Tung University)

キーワード:Optical Trapping, Cooperative Protein Assembly, Fluorescence Imaging

Optical trapping is known as a non-mechanical method of manipulating microparticles (MPs) and living cells in solution, while our group has demonstrated disk-like structure formation of the diameter of a few ten micrometers of nanoparticles (NPs) and proteins1 along the solution surface. Cooperative optical trapping of two materials (polystyrene NP, Au NP, polymer, and protein) does not simply give their mixture assembly but shows their characteristic organization. In the case of lysozyme and polyethylene glycol with 20,000 degrees of polymerization (PEG-20k), the latter macromolecular crowding agent accelerates the lysozyme assembling at and around the focus.2 Here we report its spatio-temporal characteristics revealed by fluorescence imaging and Raman scattering micro-spectroscopy.
In Figure 1a, lysozyme assembly in the 375 mg/mL solution is visualized by scanning confocal fluorescence imaging of 0.03% added RhB-bonded lysozyme, which is widely expanded around the focus. The half of lysozyme is replaced by PEG-20k and the observed result is given in Figure 1b. The lysozyme distribution is narrower and shows a sharp gradient, although the lysozyme concentration is half. The results are supported by Raman spectra and their non-negative matrix factorization analysis, which is now systematically extended. A new cooperative trapping behavior will be discussed.
1. Po-Wei Yi et al., J. Phys, Chem. C, 125, 18988 (2021).
2. W.-H. Chiu et al., JSAP Spring Meeting (2022)