High-throughput screening of optimal solution conditions for structural biological studies by fluorescence correlation spectroscopy

被引:13
作者
Sugiki, Toshihiko [2 ,3 ]
Yoshiura, Chie [1 ]
Kofuku, Yutaka [1 ]
Ueda, Takumi [1 ]
Shimada, Ichio [1 ,3 ]
Takahashi, Hideo [3 ]
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Bunkyo Ku, Tokyo 1130033, Japan
[2] JBiC, Koto Ku, Tokyo 1358073, Japan
[3] Natl Inst Adv Ind Sci & Technol, Biomed Informat Res Ctr BIRC, Koto Ku, Tokyo 1350064, Japan
关键词
protein aggregation; fluorescent correlation spectroscopy; NMR; MIP-1; alpha; PROTEIN SOLUBILITY; NMR; CRYSTALLIZATION; AGGREGATION; MIP-1-ALPHA; SYSTEM; CELLS;
D O I
10.1002/pro.92
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein aggregation is an essential molecular event in a wide variety of biological situations, and is a causal factor in several degenerative diseases. The aggregation of proteins also frequently hampers structural biological analyses, such as solution NMR studies. Therefore, precise detection and characterization of protein aggregation are of crucial importance for various research fields. In this study, we demonstrate that fluorescence correlation spectroscopy (FCS) using a single-molecule fluorescence detection system enables the detection of otherwise invisible aggregation of proteins at higher protein concentrations, which are suitable for structural biological experiments, and consumes relatively small amounts of protein over a short measurement time. Furthermore, utilizing FCS, we established a method for high-throughput screening of protein aggregation and optimal solution conditions for structural biological experiments.
引用
收藏
页码:1115 / 1120
页数:6
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