| Literature DB >> 28295928 |
Oliva Saldanha1, Rita Graceffa1,2, Clément Y J Hémonnot1, Christiane Ranke1, Gerrit Brehm1, Marianne Liebi3,4, Benedetta Marmiroli5, Britta Weinhausen6,2, Manfred Burghammer6,7, Sarah Köster1.
Abstract
Encapsulating reacting biological or chemical samples in microfluidic droplets has the great advantage over single-phase flows of providing separate reaction compartments. These compartments can be filled in a combinatoric way and prevent the sample from adsorbing to the channel walls. In recent years, small-angle X-ray scattering (SAXS) in combination with microfluidics has evolved as a nanoscale method of such systems. Here, we approach two major challenges associated with combining droplet microfluidics and SAXS. First, we present a simple, versatile, and reliable device, which is both suitable for stable droplet formation and compatible with in situ X-ray measurements. Second, we solve the problem of "diluting" the sample signal by the signal from the oil separating the emulsion droplets by multiple fast acquisitions per droplet and data thresholding. We show that using our method, even the weakly scattering protein vimentin provides high signal-to-noise ratio data.Entities:
Keywords: cytoskeletal intermediate filaments; microfluidics; small-angle X-ray scattering; vimentin; water-in-oil emulsions
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Year: 2017 PMID: 28295928 DOI: 10.1002/cphc.201700221
Source DB: PubMed Journal: Chemphyschem ISSN: 1439-4235 Impact factor: 3.102