School of Life Science and Technology, Tokyo Institute of Technology, Midori-ku, Yokohama 226-8501, Japan.
Synchrotron Radiation Life Science Instrumentation Unit, RIKEN/SPring-8 Center, Sayo-cho, Sayo-gun, Hyogo 679-5148, Japan.
Proc Natl Acad Sci U S A. 2024 Jun 18;121(25):e2322452121. doi: 10.1073/pnas.2322452121. Epub 2024 Jun 11.
Intrinsically disordered proteins (IDPs) play a crucial role in various biological phenomena, dynamically changing their conformations in response to external environmental cues. To gain a deeper understanding of these proteins, it is essential to identify the determinants that fix their structures at the atomic level. Here, we developed a pipeline for rapid crystal structure analysis of IDP using a cell-free protein crystallization (CFPC) method. Through this approach, we successfully demonstrated the determination of the structure of an IDP to uncover the key determinants that stabilize its conformation. Specifically, we focused on the 11-residue fragment of c-Myc, which forms an α-helix through dimerization with a binding partner protein. This fragment was strategically recombined with an in-cell crystallizing protein and was expressed in a cell-free system. The resulting crystal structures of the c-Myc fragment were successfully determined at a resolution of 1.92 Å and we confirmed that they are identical to the structures of the complex with the native binding partner protein. This indicates that the environment of the scaffold crystal can fix the structure of c-Myc. Significantly, these crystals were obtained directly from a small reaction mixture (30 µL) incubated for only 72 h. Analysis of eight crystal structures derived from 22 mutants revealed two hydrophobic residues as the key determinants responsible for stabilizing the α-helical structure. These findings underscore the power of our CFPC screening method as a valuable tool for determining the structures of challenging target proteins and elucidating the essential molecular interactions that govern their stability.
无规卷曲蛋白(IDP)在各种生物现象中发挥着关键作用,它们能够动态地改变构象以响应外部环境线索。为了更深入地了解这些蛋白质,确定在原子水平上固定其结构的决定因素至关重要。在这里,我们开发了一种使用无细胞蛋白结晶(CFPC)方法快速分析 IDP 晶体结构的流水线。通过这种方法,我们成功地确定了一种 IDP 的结构,揭示了稳定其构象的关键决定因素。具体来说,我们专注于 c-Myc 的 11 个残基片段,该片段通过与结合伙伴蛋白的二聚化形成α-螺旋。这个片段被策略性地与一个在细胞内结晶的蛋白重组,并在无细胞系统中表达。该 c-Myc 片段的晶体结构以 1.92 Å 的分辨率成功确定,我们证实它们与天然结合伙伴蛋白的复合物结构相同。这表明支架晶体的环境可以固定 c-Myc 的结构。重要的是,这些晶体直接从仅孵育 72 小时的 30 µL 小反应混合物中获得。对来自 22 个突变体的 8 个晶体结构的分析揭示了两个疏水性残基作为稳定α-螺旋结构的关键决定因素。这些发现强调了我们的 CFPC 筛选方法的强大功能,它是一种确定具有挑战性的靶蛋白结构并阐明控制其稳定性的基本分子相互作用的有价值工具。