Continuous organelle separation in an insulator‐based dielectrophoretic device. Issue 12 (14th June 2022)

• Record Type: Journal Article
• Authors: Ortiz, Ricardo; Koh, Domin; Kim, Dai Hyun; Rabbani, Mohammad Towshif; Anguaya Velasquez, Cesar; Sonker, Mukul; Arriaga, Edgar A.; Ros, Alexandra
• Other Names: Hayes Mark guestEditor.; Flanagan Lisa guestEditor.; Martinez‐Duarte Rodrigo guestEditor.
• Is Part Of: Electrophoresis. Volume 43:Issue 12(2022)
• Page Start: 1283
• Page End: 1296
• Publication Date: 2022-06-14
• Subjects: continuous separation -- insulator‐based dielectrophoresis -- mitochondria -- ratchet -- size‐based separation; Electrophoresis -- Periodicals; Electrophoresis -- Periodicals; 541.372
• DOI: 10.1002/elps.202100326
• Languages: English
• ISSNs: 0173-0835

Abstract

Abstract: Heterogeneity in organelle size has been associated with devastating human maladies such as neurodegenerative diseases or cancer. Therefore, assessing the size‐based subpopulation of organelles is imperative to understand the biomolecular foundations of these diseases. Here, we demonstrated a ratchet migration mechanism using insulator‐based dielectrophoresis in conjunction with a continuous flow component that allows the size‐based separation of submicrometer particles. The ratchet mechanism was realized in a microfluidic device exhibiting an array of insulating posts, tailoring electrokinetic and dielectrophoretic transport. A numerical model was developed to elucidate the particle migration and the size‐based separation in various conditions. Experimentally, the size‐based separation of a mixture of polystyrene beads (0.28 and 0.87 μ $\umu $ m) was accomplished demonstrating good agreement with the numerical model. Furthermore, the size‐based separation of mitochondria was investigated using a mitochondria mixture isolated from HepG2 cells and HepG2 cells carrying the gene Mfn‐1 knocked out, indicating distinct size‐related migration behavior. With the presented continuous flow separation device, larger amounts of fractionated organelles can be collected in the future allowing access to the biomolecular signature of mitochondria subpopulations differing in size.