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Austria;;
DOI:10.1021/acs.analchem.2c03168.png)
摘要
En 中文
Microfluidic diffusional sizing (MDS) is a recent and powerful method for determining the hydrodynamic sizes and interactions of biomolecules and nanoparticles. A major benefit of MDS is that it can report the size of a fluorescently labeled target even in mixtures with complex, unpurified samples. However, a limitation of MDS is that the target itself has to be purified and covalently labeled with a fluorescent dye. Such covalent labeling is not suitable for crude extracts such as native nanodiscs directly obtained from cellular membranes. In this study, we introduce fluorescent universal lipid labeling for MDS (FULL-MDS) as a sparse, noncovalent labeling method for determining particle size. We first demonstrate that the inexpensive and well-characterized fluorophore, Nile blue, spontaneously partitions into lipid nanoparticles without disrupting their structure. We then highlight the key advantage of FULL-MDS by showing that it yields robust size information on lipid nanoparticles in crude cell extracts that are not amenable to other sizing methods. Furthermore, even for synthetic nanodiscs, FULL-MDS is faster, cheaper, and simpler than existing labeling schemes.
Keyword:
NILE RED
BLUE
BODIPY
SIZES
DYE
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期刊
IF:
6.7
论文数:
4.7W
被引数:
15.9W
机构
引用论文
A bioinspired glycopolymer for capturing membrane proteins in native-like lipid-bilayer nanodiscs
NANOSCALE
IF5.1
Self-Assembly of Protein-Containing Lipid-Bilayer Nanodiscs from Small-Molecule Amphiphiles小分子两亲分子自组装含蛋白质的脂质双层纳米盘
SMALL
IF12.1
Microfluidic Diffusion Analysis of the Sizes and Interactions of Proteins under Native Solution Conditions
ACS NANO
IF16
Microfluidic Diffusion Platform for Characterizing the Sizes of Lipid Vesicles and the Thermodynamics of Protein-Lipid Interactions
ANALYTICAL CHEMISTRY
IF6.7

