期刊
IUCRJ
卷 8, 期 -, 页码 186-194出版社
INT UNION CRYSTALLOGRAPHY
DOI: 10.1107/S2052252520016243
关键词
cryo-EM; devitrification; beam-induced movement
资金
- Max-Planck-Gesellschaft
Cryo-EM technology is facing challenges in high-resolution structure determination of biological specimens due to beam-induced movement. Controlled devitrification of frozen samples reduces movement and enhances structure quality, contributing significantly to achieving high-resolution structure determination.
As cryo-EM approaches the physical resolution limits imposed by electron optics and radiation damage, it becomes increasingly urgent to address the issues that impede high-resolution structure determination of biological specimens. One of the persistent problems has been beam-induced movement, which occurs when the specimen is irradiated with high-energy electrons. Beam-induced movement results in image blurring and loss of high-resolution information. It is particularly severe for biological samples in unsupported thin films of vitreous water. By controlled devitrification of conventionally plunge-frozen samples, the suspended film of vitrified water was converted into cubic ice, a polycrystalline, mechanically stable solid. It is shown that compared with vitrified samples, devitrification reduces beam-induced movement in the first 5 e angstrom(-2) of an exposure by a factor of similar to 4, substantially enhancing the contribution of the initial, minimally damaged frames to a structure. A 3D apoferritin map reconstructed from the first frames of 20 000 particle images of devitrified samples resolved undamaged side chains. Devitrification of frozen-hydrated specimens helps to overcome beam-induced specimen motion in single-particle cryo-EM, as a further step towards realizing the full potential of cryo-EM for high-resolution structure determination.
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