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OCRE 剪接因子 RBM5 和 RBM10 的结构域:通过 1 H NMR 光谱和分子动力学模拟的综合应用确定的酪氨酸环翻转频率。

OCRE Domains of Splicing Factors RBM5 and RBM10: Tyrosine Ring-Flip Frequencies Determined by Integrated Use of H NMR Spectroscopy and Molecular Dynamics Simulations.

机构信息

Department of Integrative Structural and Computational Biology, The Scripps Research Institute, 10550 N. Torrey Pines Road, MB 44, La Jolla, CA 92037, USA.

Present address: Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USA.

出版信息

Chembiochem. 2021 Feb 2;22(3):565-570. doi: 10.1002/cbic.202000517. Epub 2020 Nov 4.

DOI:10.1002/cbic.202000517
PMID:32975902
Abstract

The 55-residue OCRE domains of the splicing factors RBM5 and RBM10 contain 15 tyrosines in compact, globular folds. At 25 °C, all 15 tyrosines show symmetric H NMR spectra, with averaged signals for the pairs of δ- and ϵ-ring hydrogens. At 4 °C, two tyrosines were identified as showing H NMR line-broadening due to lowered frequency of the ring-flipping. For the other 13 tyrosine rings, it was not evident, from the H NMR data alone, whether they were either all flipping at high frequencies, or whether slowed flipping went undetected due to small chemical-shift differences between pairs of exchanging ring hydrogen atoms. Here, we integrate H NMR spectroscopy and molecular dynamics (MD) simulations to determine the tyrosine ring-flip frequencies. In the RBM10-OCRE domain, we found that, for 11 of the 15 tyrosines, these frequencies are in the range 2.0×10 to 1.3×10  s , and we established an upper limit of <1.0×10  s for the remaining four residues. The experimental data and the MD simulation are mutually supportive, and their combined use extends the analysis of aromatic ring-flip events beyond the limitations of routine H NMR line-shape analysis into the nanosecond frequency range.

摘要

剪接因子 RBM5 和 RBM10 的 55 残基 OCRE 结构域包含 15 个酪氨酸,这些酪氨酸位于紧凑的球形折叠中。在 25°C 下,所有 15 个酪氨酸的 H NMR 谱均显示对称信号,δ-和 ε-环氢的平均信号。在 4°C 下,由于环翻转频率降低,有两个酪氨酸被鉴定为 H NMR 线展宽。对于其他 13 个酪氨酸环,仅从 H NMR 数据来看,无法确定它们是否都以高频翻转,或者由于交换环氢原子之间的化学位移差异较小,因此翻转速度较慢而未被检测到。在这里,我们整合 H NMR 光谱和分子动力学(MD)模拟来确定酪氨酸环翻转频率。在 RBM10-OCRE 结构域中,我们发现 15 个酪氨酸中的 11 个的这些频率在 2.0×10 到 1.3×10 s 范围内,我们还确定了其余四个残基的翻转频率上限<1.0×10 s。实验数据和 MD 模拟相互支持,它们的组合使用将芳香环翻转事件的分析扩展到常规 H NMR 线形分析的限制之外,进入纳秒频率范围。

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