Department of Medicinal Chemistry, University of Washington, Seattle, WA 98195-7610, United States of America.
Department of Chemistry and Biochemistry, Florida International University, Miami, FL 33199, United States of America.
J Inorg Biochem. 2023 Jul;244:112211. doi: 10.1016/j.jinorgbio.2023.112211. Epub 2023 Apr 5.
Cytochrome P450 3A4 (CYP3A4) metabolizes a wide range of drugs and toxins. Interactions of CYP3A4 with ligands are difficult to predict due to promiscuity and conformational flexibility. To better understand CYP3A4 conformational responses to ligands we use hydrogen deuterium exchange mass spectrometry (HDX-MS) to investigate the effect of ligands on nanodisc-embedded CYP3A4. For a subset of CYP3A4-ligand complexes, differences in the low-frequency modes derived by principal component analyses of molecular dynamics trajectories mirrored the HDX-MS results. The effects of ligands are distributed to flexible elements of CYP3A4 between stretches of secondary structure. The largest effects occur in the F- and G-helices, where most ligands increase the flexibility of the F-helix and connecting loops and decrease the flexibility of the C-term of the G-helix. Most ligands affect the E-F-G, CD and HI regions of the protein. Ligand-dependent differences are observed in the A"-A' loop, BC region, E-helix, K-β1 region, proximal loop, and C-term loop. Correlated HDX responses were observed in the CD region and the C-term of the G-helix that were most pronounced for Type II ligands. Collectively, the HDX and molecular dynamics results suggest that CYP3A4 accommodates diverse binding partners by propagating local backbone fluctuations from the binding site onto the flexible regions of the enzyme via long-range interactions that are differentially modulated by ligands. In contrast to the paradigm wherein ligands decrease protein dynamics at their binding site, a wide range of ligands modestly increase CYP3A4 dynamics throughout the protein including effects remote from the active site.
细胞色素 P450 3A4(CYP3A4)代谢广泛的药物和毒素。由于混杂性和构象灵活性,CYP3A4 与配体的相互作用难以预测。为了更好地了解 CYP3A4 对配体的构象响应,我们使用氢氘交换质谱(HDX-MS)来研究配体对纳米盘嵌入 CYP3A4 的影响。对于 CYP3A4-配体复合物的一部分,主成分分析分子动力学轨迹得出的低频模式的差异反映了 HDX-MS 的结果。配体的作用分布在二级结构之间的 CYP3A4 的柔性元件上。最大的影响发生在 F 和 G 螺旋中,大多数配体增加 F 螺旋和连接环的灵活性,降低 G 螺旋 C 端的灵活性。大多数配体影响蛋白质的 EF-G、CD 和 HI 区域。在 A"-A' 环、BC 区域、E 螺旋、K-β1 区域、近端环和 C 端环中观察到配体依赖性差异。在 CD 区域和 G 螺旋的 C 端观察到相关的 HDX 响应,对于 II 型配体最为明显。总的来说,HDX 和分子动力学结果表明,CYP3A4 通过从结合位点传播局部骨架波动通过远程相互作用将配体对酶的柔性区域进行传播,从而适应不同的结合伙伴。与配体在其结合位点降低蛋白质动力学的范例相反,广泛的配体适度增加 CYP3A4 的动力学,包括远离活性位点的影响。