Institute of High Technologies, Taras Shevchenko National University of Kyiv, Kyiv, 01601, Ukraine.
Biophysics Laboratories, School of Biology, University of Portsmouth, Portsmouth, PO1 2DT, UK.
Eur Biophys J. 2021 Jul;50(5):787-792. doi: 10.1007/s00249-021-01520-w. Epub 2021 Apr 24.
Analysis of calorimetric and crystallographic information shows that the α-helix is maintained not only by the hydrogen bonds between its polar peptide groups, as originally supposed, but also by van der Waals interactions between tightly packed apolar groups in the interior of the helix. These apolar contacts are responsible for about 60% of the forces stabilizing the folded conformation of the α-helix and their exposure to water on unfolding results in the observed heat capacity increment, i.e. the temperature dependence of the melting enthalpy. The folding process is also favoured by an entropy increase resulting from the release of water from the peptide groups. A similar situation holds for the DNA double helix: calorimetry shows that the hydrogen bonding between conjugate base pairs provides a purely entropic contribution of about 40% to the Gibbs energy while the enthalpic van der Waals interactions between the tightly packed apolar parts of the base pairs provide the remaining 60%. Despite very different structures, the thermodynamic basis of α-helix and B-form duplex stability are strikingly similar. The general conclusion follows that the stability of protein folds is primarily dependent on internal atomic close contacts rather than the hydrogen bonds they contain.
分析量热和晶体学信息表明,α-螺旋不仅像最初假设的那样通过其极性肽基团之间的氢键来维持,而且还通过紧密堆积的疏水性基团内部的范德华相互作用来维持。这些疏水性接触负责稳定α-螺旋折叠构象的大约 60%的力,它们在展开时暴露于水中会导致观察到的热容增量,即熔化焓的温度依赖性。折叠过程也受到从肽基团释放水导致的熵增加的促进。DNA 双螺旋也存在类似的情况:量热法表明,共轭碱基对之间的氢键提供了大约 40%的纯熵贡献,而碱基对紧密堆积的疏水性部分之间的焓范德华相互作用提供了剩余的 60%。尽管结构非常不同,但α-螺旋和 B 型双链体稳定性的热力学基础惊人地相似。一般结论是,蛋白质折叠的稳定性主要取决于内部原子的紧密接触,而不是它们所包含的氢键。