Two-stage optical trapping and assembling of protein at air/solution interface

被引:5
|
作者
Yi, Po-Wei [1 ,2 ]
Chiu, Wei-Hsiang [1 ]
Toyouchi, Shuichi [1 ]
Bresoli-Obach, Roger [1 ,3 ,4 ]
Hofkens, Johan [3 ,5 ]
Chatani, Eri [6 ]
Hosokawa, Yoichiroh [2 ]
Sugiyama, Teruki [1 ,2 ,7 ]
Masuhara, Hiroshi [1 ,7 ]
机构
[1] Natl Yang Ming Chiao Tung Univ, Dept Appl Chem, Hsinchu, Taiwan
[2] Nara Inst Sci & Technol, Div Mat Sci, Ikoma 6300192, Japan
[3] Katholieke Univesiteit Leuven, Dept Chem, B-3001 Heverlee, Belgium
[4] Univ Ramon Llull, Inst Quim Sarria, Barcelona 08007, Spain
[5] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
[6] Kobe Univ, Dept Chem, Kobe 6578501, Japan
[7] Natl Yang Ming Chiao Tung Univ, Ctr Emergent Funct Matter Sci, Hsinchu 300093, Taiwan
基金
日本学术振兴会;
关键词
optical trapping; lysozyme; protein cluster; solution surface; multiplane microscope; polystyrene microparticle; CHEMISTRY; PHASE;
D O I
10.35848/1882-0786/acb3ab
中图分类号
O59 [应用物理学];
学科分类号
摘要
Optical trapping at interfaces has recently gained relevance due to the expansion of optical potential far away from the focus, especially for proteins where submillimeter structures have been described. Initially, lysozyme clusters are trapped as a shallow layer at the surface, becoming thicker with irradiation time. Nonetheless, overcoming a concentration threshold, lysozyme clusters inside the solution are collected and transported toward the focus, invading the lysozyme layer, which results in a border between them, although no concentration jump is detected. This two-stage optical trapping occurs due to the long-range interaction originating from the focus.
引用
收藏
页数:7
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