| Literature DB >> 25522818 |
Hiroyuki Yamakoshi1, Almar Palonpon2, Kosuke Dodo3, Jun Ando4, Satoshi Kawata5, Katsumasa Fujita6, Mikiko Sodeoka7.
Abstract
We previously showed that bisarylbutadiyne (BADY), which has a conjugated diyne structure, exhibits an intense peak in the cellular Raman-silent region. Here, we synthesized a mitochondria-selective Raman probe by linking bisphenylbutadiyne with triphenylphosphonium, a well-known mitochondrial targeting moiety. This probe, named MitoBADY, has a Raman peak 27 times more intense than that of 5-ethynyl-2'-deoxyuridine. Raman microscopy using submicromolar extracellular probe concentrations successfully visualized mitochondria in living cells. A full Raman spectrum is acquired at each pixel of the scanned sample, and we showed that simultaneous Raman imaging of MitoBADY and endogenous cellular biomolecules can be achieved in a single scan. MitoBADY should be useful for the study of mitochondrial dynamics.Entities:
Keywords: Imaging; Live cell; Mitochondria; Raman; Triphenylphosphonium
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Year: 2014 PMID: 25522818 DOI: 10.1016/j.bmcl.2014.11.080
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823