| Literature DB >> 33164530 |
Nathan D Williams1,2, Ane Landajuela2,3, Ravi Kiran Kasula1, Wenjiao Zhou1,2, John T Powell1,2, Zhiqun Xi1, Farren J Isaacs4,5,6, Julien Berro1,2,7, Derek Toomre1, Erdem Karatekin2,3,7,8, Chenxiang Lin1,2.
Abstract
Fluorescence microscopy has been one of the most discovery-rich methods in biology. In the digital age, the discipline is becoming increasingly quantitative. Virtually all biological laboratories have access to fluorescence microscopes, but abilities to quantify biomolecule copy numbers are limited by the complexity and sophistication associated with current quantification methods. Here, we present DNA-origami-based fluorescence brightness standards for counting 5-300 copies of proteins in bacterial and mammalian cells, tagged with fluorescent proteins or membrane-permeable organic dyes. Compared to conventional quantification techniques, our brightness standards are robust, straightforward to use, and compatible with nearly all fluorescence imaging applications, thereby providing a practical and versatile tool to quantify biomolecules via fluorescence microscopy.Entities:
Keywords: Bioconjugation; Brightness standard; DNA origami; Fluorescent protein; Live cell imaging; Quantitative microscopy
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Year: 2020 PMID: 33164530 PMCID: PMC7726105 DOI: 10.1021/acs.nanolett.0c03925
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189