| Literature DB >> 27316458 |
Daisuke Matsumoto1, Ayana Yamagishi2, Megumi Saito1, Ramachandra Rao Sathuluri2, Yaron R Silberberg2, Futoshi Iwata3, Takeshi Kobayashi4, Chikashi Nakamura5.
Abstract
Efficient and rapid delivery of macromolecule probes, such as quenchbodies and other large biomarkers that cannot readily pass through the plasma membrane, is necessary for live-cell imaging and other intracellular analyses. We present here an alternative, simple method for delivery of macromolecules into live cells. In this method, which we term here mechanoporation, a nanoneedle array is used for making transient pores in the plasma membrane to allow access of desired macromolecules into thousands of live cells, simultaneously. This rapid, 3-step method facilitates an efficient delivery by adding macromolecules into the medium, inserting nanoneedles into the cells and oscillating the nanoneedle array, a process that takes no more than 5 min in total. In addition, we demonstrate here how this method can repeatedly and reproducibly deliver molecules into specifically-selected locations on a given cell culture dish. The results presented here show how this unique mechanoporation method enables rapid and high-throughput bio-macromolecule delivery and live-cell imaging. Copyright ÂKeywords: Continuous and rapid delivery; Mammalian cells; Mechanoporation; Nanoneedle array; Position-specific delivery
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Year: 2016 PMID: 27316458 DOI: 10.1016/j.jbiosc.2016.05.006
Source DB: PubMed Journal: J Biosci Bioeng ISSN: 1347-4421 Impact factor: 2.894