TY - JOUR
T1 - Rapid Acquisition of X-Ray Scattering Data from Droplet-Encapsulated Protein Systems
AU - Saldanha, Oliva
AU - Graceffa, Rita
AU - Hémonnot, Clément Y.J.
AU - Ranke, Christiane
AU - Brehm, Gerrit
AU - Liebi, Marianne
AU - Marmiroli, Benedetta
AU - Weinhausen, Britta
AU - Burghammer, Manfred
AU - Köster, Sarah
PY - 2017/5
Y1 - 2017/5
N2 - 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.
AB - 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.
KW - cytoskeletal intermediate filaments
KW - microfluidics
KW - small-angle X-ray scattering
KW - vimentin
KW - water-in-oil emulsions
UR - https://www.scopus.com/pages/publications/85017578770
U2 - 10.1002/cphc.201700221
DO - 10.1002/cphc.201700221
M3 - Article
C2 - 28295928
AN - SCOPUS:85017578770
SN - 1439-4235
VL - 18
SP - 1220
EP - 1223
JO - ChemPhysChem
JF - ChemPhysChem
IS - 10
ER -