Mashayekhi Ghoncheh, Vant John, Polavarapu Abhigna, Ourmazd Abbas, Singharoy Abhishek
Department of Physics, University of Wisconsin Milwaukee, 3135 N. Maryland Ave, Milwaukee, WI, 53211, USA.
School of Molecular Sciences, Center for Applied Structural Discovery, Arizona State University, Tempe, AZ, 85287, USA.
Curr Res Struct Biol. 2022;4:68-77. doi: 10.1016/j.crstbi.2022.02.001. Epub 2022 Mar 8.
Cryo-electron microscopy (cryo-EM) has produced a number of structural models of the SARS-CoV-2 spike, already prompting biomedical outcomes. However, these reported models and their associated electrostatic potential maps represent an unknown admixture of conformations stemming from the underlying energy landscape of the spike protein. As with any protein, some of the spike's conformational motions are expected to be biophysically relevant, but cannot be interpreted only by static models. Using experimental cryo-EM images, we present the energy landscape of the glycosylated spike protein, and identify the diversity of low-energy conformations in the vicinity of its open (so called 1RBD-up) state. The resulting atomic refinement reveal global and local molecular rearrangements that cannot be inferred from an average 1RBD-up cryo-EM model. Here we report varied degrees of "openness" in global conformations of the 1RBD-up state, not revealed in the single-model interpretations of the density maps, together with conformations that overlap with the reported models. We discover how the glycan shield contributes to the stability of these low-energy conformations. Five out of six binding sites we analyzed, including those for engaging ACE2, therapeutic mini-proteins, linoleic acid, two different kinds of antibodies, switch conformations between their known apo- and holo-conformations, even when the global spike conformation is 1RBD-up. This apo-to-holo switching is reminiscent of a conformational preequilibrium. We found only one binding site, namely that of AB-C135 remains in apo state within all the sampled free energy-minimizing models, suggesting an induced fit mechanism for the docking of this antibody to the spike.
冷冻电子显微镜(cryo-EM)已生成了多种严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白的结构模型,这些模型已经推动了生物医学成果的产生。然而,这些已报道的模型及其相关的静电势图代表了源自刺突蛋白潜在能量景观的未知构象混合物。与任何蛋白质一样,刺突蛋白的一些构象运动预计在生物物理上具有相关性,但不能仅通过静态模型来解释。利用实验性冷冻电子显微镜图像,我们展示了糖基化刺突蛋白的能量景观,并确定了其开放(即所谓的1RBD向上)状态附近低能量构象的多样性。由此产生的原子精修揭示了无法从平均的1RBD向上冷冻电子显微镜模型推断出的全局和局部分子重排。在这里,我们报告了1RBD向上状态全局构象中不同程度的“开放性”,这在密度图的单模型解释中未被揭示,同时还有与已报道模型重叠的构象。我们发现聚糖屏蔽如何有助于这些低能量构象的稳定性。我们分析的六个结合位点中有五个,包括那些与血管紧张素转换酶2(ACE2)、治疗性微型蛋白、亚油酸、两种不同抗体结合的位点,即使在刺突蛋白全局构象为1RBD向上时,它们在已知的无配体和有配体构象之间也会切换构象。这种无配体到有配体的切换让人联想到构象预平衡。我们发现只有一个结合位点,即AB-C135的结合位点在所有采样的自由能最小化模型中都保持无配体状态,这表明该抗体与刺突蛋白对接存在诱导契合机制。