The 65h JSAP Spring Meeting, 2018

Presentation information

Oral presentation

12 Organic Molecules and Bioelectronics » 12.7 Biomedical Engineering and Biochips

[18p-F306-1~17] 12.7 Biomedical Engineering and Biochips

Sun. Mar 18, 2018 1:45 PM - 6:30 PM F306 (61-306)

Koichiro Miyamoto(Tohoku Univ.), Hideaki Yamamoto(Tohoku Univ.), Shin Yokoyama(Hiroshima Univ.)

2:15 PM - 2:30 PM

[18p-F306-3] Pattern size effect in exosome array

〇(PC)Kyohei Okubo1, Hiromi Kuramochi1, Akiko Iwaya1, Shoichi Tsuchiya2, Rei Okamura1, Takanori Ichiki1,2 (1.The Univ. of Tokyo, 2.iCONM)

Keywords:Single particle analysis, Exosome, Array chip technology

Exosomes, one of extracellular vesicles in size ranging from 30–150 nm in diameter, have recently attracted much attention as promising biomarker for an early stage diagnostic test. Here, we propose an assay platform called exosome array on which exosomes are separately immobilized and analyzed in the similar manner as DNA array. Polyethyleneglycol (PEG)-lipid modified nanodot array is formed on the Si substrate by a combination of electron beam lithography, selective chemical modification, and lift-off process. PEG-lipid derivative has an oleyl group at its end, at which exosomes are attached via hydrophobic interaction. Exosomal suspension derived from leukemia HL60 cells are flown over the array. The topography of the dotarray was observed using atomic force microscope, revealing single exosome was tethered on the array. In presentation, we will discuss the effect of dotarray pattern size on attached exosomes.