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