Cell-free protein crystallization for nanocrystal structure determination

被引:13
作者
Abe, Satoshi [1 ]
Tanaka, Junko [1 ]
Kojima, Mariko [1 ]
Kanamaru, Shuji [1 ]
Hirata, Kunio [2 ]
Yamashita, Keitaro [2 ,4 ]
Kobayashi, Ayako [1 ]
Ueno, Takafumi [1 ,3 ]
机构
[1] Tokyo Inst Technol, Sch Life Sci & Technol, Midori Ku, Nagatsuta Cho 4259, Yokohama, Kanagawa 2268501, Japan
[2] RIKEN SPring 8 Ctr, SR Life Sci Instrumentat Unit, 1-1-1 Kouto, Sayo, Hyogo 6795148, Japan
[3] Tokyo Inst Technol, Int Res Frontiers Initiat IRFI, Midori Ku, Nagatsuta Cho 4259, Yokohama, Kanagawa 2268501, Japan
[4] MRC Lab Mol Biol, Francis Crick Ave, Cambridge CB2 0QH, England
基金
日本科学技术振兴机构;
关键词
REFINEMENT; CRYSTALS; SYSTEM;
D O I
10.1038/s41598-022-19681-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In-cell protein crystallization (ICPC) has been investigated as a technique to support the advancement of structural biology because it does not require protein purification and a complicated crystallization process. However, only a few protein structures have been reported because these crystals formed incidentally in living cells and are insufficient in size and quality for structure analysis. Here, we have developed a cell-free protein crystallization (CFPC) method, which involves direct protein crystallization using cell-free protein synthesis. We have succeeded in crystallization and structure determination of nano-sized polyhedra crystal (PhC) at a high resolution of 1.80 angstrom. Furthermore, nanocrystals were synthesized at a reaction scale of only 20 mu L using the dialysis method, enabling structural analysis at a resolution of 1.95 angstrom. To further demonstrate the potential of CFPC, we attempted to determine the structure of crystalline inclusion protein A (CipA), whose structure had not yet been determined. We added chemical reagents as a twinning inhibitor to the CFPC solution, which enabled us to determine the structure of CipA at 2.11 angstrom resolution. This technology greatly expands the high-throughput structure determination method of unstable, low-yield, fusion, and substrate-biding proteins that have been difficult to analyze with conventional methods.
引用
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页数:11
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