Microflow-mediated optical assembly of nanoparticles with femtogram protein via shrinkage of light-induced bubbles
Mayu Ueda,
Yushi Nishimura,
Mamoru Tamura,
Syoji Ito,
Shiho Tokonami,
Takuya Iida
Affiliations
Mayu Ueda
Department of Physical Science, Graduate School of Science, Osaka Prefecture University, Sakai, Osaka 599-8570, Japan
Yushi Nishimura
Division of Molecular Materials Science, Graduate School of Science, Osaka City University, Sumiyoshi-ku, Osaka 558-8585, Japan
Mamoru Tamura
Department of Physical Science, Graduate School of Science, Osaka Prefecture University, Sakai, Osaka 599-8570, Japan
Syoji Ito
Division of Frontier Materials Science, Graduate School of Engineering Science, Osaka University, 1-3, Machikaneyama-cho, Toyonaka, Osaka 560-8531, Japan
Shiho Tokonami
Department of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, Sakai 599-8570, Japan
Takuya Iida
Department of Physical Science, Graduate School of Science, Osaka Prefecture University, Sakai, Osaka 599-8570, Japan
Bottom-up processing of nanobiomaterials enables the creation of a variety of macroscopic structures in natural systems. Here, we use optical means to produce macroscopic-assembled structures of nanoparticles (NPs) from protein molecules by using light-induced bubble (LIB) generation under asymmetric pressure-driven flow in a microchannel. The broadband optical response of assembled NPs facilitates the application of photon pressure and photothermal convection when irradiated by using an infrared laser. The presence of a large amount of protein allows the generation of a vast number of stable LIBs from optically assembled metallic NP-fixed beads (MNFBs). In the case of more diluted albumin solutions, the shrinking of a single LIB can cause the aggregation of MNFBs via fg-level albumin (3.4 fg in the observation region), like a microscale bubblegum. The size of the resulting aggregate can be controlled by changing the concentration of protein. These findings can be used to devise production methods not only for broadband optical nanocomposites but also for label-free methods to detect an extremely small amount of protein.