Robert F. Smith School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, New York; Department of Chemistry and Chemical Biology, Cornell University, Ithaca, New York.
Department of Microbiology and Immunology, Cornell University, Ithaca, New York.
Biophys J. 2023 Feb 21;122(4):646-660. doi: 10.1016/j.bpj.2023.01.016. Epub 2023 Jan 16.
We address the challenge of understanding how hydrophobic interactions are encoded by fusion peptide (FP) sequences within coronavirus (CoV) spike proteins. Within the FPs of severe acute respiratory syndrome CoV 2 and Middle East respiratory syndrome CoV (MERS-CoV), a largely conserved peptide sequence called FP1 (SFIEDLLFNK and SAIEDLLFDK in SARS-2 and MERS, respectively) has been proposed to play a key role in encoding hydrophobic interactions that drive viral-host cell membrane fusion. Although a non-polar triad (Leu-Leu-Phe (LLF)) is common to both FP1 sequences, and thought to dominate the encoding of hydrophobic interactions, FP1 from SARS-2 and MERS differ in two residues (Phe 2 versus Ala 2 and Asn 9 versus Asp 9, respectively). Here we explore whether single-molecule force measurements can quantify hydrophobic interactions encoded by FP1 sequences, and then ask whether sequence variations between FP1 from SARS-2 and MERS lead to significant differences in hydrophobic interactions. We find that both SARS-2 and MERS wild-type FP1 generate measurable hydrophobic interactions at the single-molecule level, but that SARS-2 FP1 encodes a substantially stronger hydrophobic interaction than its MERS counterpart (1.91 ± 0.03 nN versus 0.68 ± 0.03 nN, respectively). By performing force measurements with FP1 sequences with single amino acid substitutions, we determine that a single-residue mutation (Phe 2 versus Ala 2) causes the almost threefold difference in the hydrophobic interaction strength generated by the FP1 of SARS-2 versus MERS, despite the presence of LLF in both sequences. Infrared spectroscopy and circular dichroism measurements support the proposal that the outsized influence of Phe 2 versus Ala 2 on the hydrophobic interaction arises from variation in the secondary structure adopted by FP1. Overall, these insights reveal how single-residue diversity in viral FPs, including FP1 of SARS-CoV-2 and MERS-CoV, can lead to substantial changes in intermolecular interactions proposed to play a key role in viral fusion, and hint at strategies for regulating hydrophobic interactions of peptides in a range of contexts.
我们研究了冠状病毒 (CoV) 刺突蛋白融合肽 (FP) 序列如何编码疏水性相互作用的问题。在严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2) 和中东呼吸综合征冠状病毒 (MERS-CoV) 的 FP 中,提出了一个广泛保守的肽序列,称为 FP1 (SFIEDLLFNK 和 SAIEDLLFDK 分别在 SARS-2 和 MERS 中),它在编码驱动病毒-宿主细胞膜融合的疏水性相互作用方面发挥着关键作用。尽管 FP1 序列都含有一个非极性三联体 (Leu-Leu-Phe (LLF)),并且被认为主导着疏水性相互作用的编码,但 SARS-2 和 MERS 的 FP1 在两个残基上存在差异 (Phe 2 与 Ala 2 和 Asn 9 与 Asp 9 分别)。在这里,我们探索了单分子力测量是否可以量化 FP1 序列编码的疏水性相互作用,然后询问 SARS-2 和 MERS 的 FP1 之间的序列差异是否导致疏水性相互作用的显著差异。我们发现,SARS-2 和 MERS 野生型 FP1 都在单分子水平上产生可测量的疏水性相互作用,但 SARS-2 FP1 编码的疏水性相互作用比其 MERS 对应物强得多 (分别为 1.91 ± 0.03 nN 和 0.68 ± 0.03 nN)。通过对 FP1 序列进行单氨基酸取代的力测量,我们确定一个单残基突变 (Phe 2 与 Ala 2) 导致 SARS-2 与 MERS 的 FP1 产生的疏水性相互作用强度几乎相差三倍,尽管这两种序列都存在 LLF。红外光谱和圆二色性测量支持这样的假设,即 Phe 2 与 Ala 2 对疏水性相互作用的巨大影响源于 FP1 采用的二级结构的变化。总的来说,这些研究结果揭示了病毒 FPs 中的单残基多样性,包括 SARS-CoV-2 和 MERS-CoV 的 FP1,如何导致在拟议的病毒融合中发挥关键作用的分子间相互作用的显著变化,并暗示了在多种情况下调节肽的疏水性相互作用的策略。