Molecular Biophysics, Imperial College London, South Kensington Campus, London SW7 2AZ, UK.
Protein Crystallography Facility, Centre for Structural Biology, Flowers Building, Department of Life Sciences, Imperial College London, London SW7 2AZ, UK.
Int J Mol Sci. 2017 Sep 7;18(9):1918. doi: 10.3390/ijms18091918.
The photochromic fluorescent protein Skylan-NS (Nonlinear Structured illumination variant mEos3.1H62L) is a reversibly photoswitchable fluorescent protein which has an unilluminated/ground state with an anionic and cis chromophore conformation and high fluorescence quantum yield. Photo-conversion with illumination at 515 nm generates a meta-stable intermediate with neutral trans-chromophore structure that has a 4 h lifetime. We present X-ray crystal structures of the cis (on) state at 1.9 Angstrom resolution and the trans (off) state at a limiting resolution of 1.55 Angstrom from serial femtosecond crystallography experiments conducted at SPring-8 Angstrom Compact Free Electron Laser (SACLA) at 7.0 keV and 10.5 keV, and at Linac Coherent Light Source (LCLS) at 9.5 keV. We present a comparison of the data reduction and structure determination statistics for the two facilities which differ in flux, beam characteristics and detector technologies. Furthermore, a comparison of droplet on demand, grease injection and Gas Dynamic Virtual Nozzle (GDVN) injection shows no significant differences in limiting resolution. The photoconversion of the on- to the off-state includes both internal and surface exposed protein structural changes, occurring in regions that lack crystal contacts in the orthorhombic crystal form.
光致变色荧光蛋白 Skylan-NS(非线性结构照明变体 mEos3.1H62L)是一种可反向光开关的荧光蛋白,它具有未被照亮/基态的阴离子和顺式发色团构象和高荧光量子产率。用 515nm 的光进行光转化会生成一个具有中性反式发色团结构的亚稳态中间产物,其寿命为 4 小时。我们通过在 SPring-8 埃科马自由电子激光(SACLA)上进行的连续飞秒晶体学实验,以 7.0keV 和 10.5keV 的能量,以及在 Linac Coherent Light Source(LCLS)上以 9.5keV 的能量,得到了顺式(开)态在 1.9Å分辨率和反式(关)态在 1.55Å极限分辨率的 X 射线晶体结构。我们对通量、光束特性和探测器技术不同的两个设施的数据还原和结构确定统计数据进行了比较。此外,液滴按需、油脂注射和气体动力学虚拟喷嘴(GDVN)注射的比较表明,在极限分辨率方面没有显著差异。从开态到关态的光致变色包括内部和表面暴露的蛋白质结构变化,这些变化发生在正交晶型中没有晶体接触的区域。