Guo Mingxia, Jones Marie J, Goh Racheal, Verma Vivek, Guinn Emily, Heng Jerry Y Y
Department of Chemical Engineering, Imperial College London, South Kensington Campus, LondonSW7 2AZ, U.K.
Synthetic Molecule Design and Development, Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana46221, United States.
Cryst Growth Des. 2023 Jan 24;23(3):1668-1675. doi: 10.1021/acs.cgd.2c01229. eCollection 2023 Mar 1.
To explore the effect of chain length and conformation on the nucleation of peptides, the primary nucleation induction time of glycine homopeptides in pure water at different supersaturation levels under various temperatures has been determined. Nucleation data suggest that longer chains will prolong the induction time, especially for chains longer than three, where nucleation will occur over several days. In contrast, the nucleation rate increased with an increase in the supersaturation for all homopeptides. Induction time and nucleation difficulty increase at lower temperatures. However, for triglycine, the dihydrate form was produced with an unfolded peptide conformation (pPII) at low temperature. The interfacial energy and activation Gibbs energy of this dihydrate form are both lower than those at high temperature, while the induction time is longer, indicating the classical nucleation theory is not suitable to explain the nucleation phenomenon of triglycine dihydrate. Moreover, gelation and liquid-liquid separation of longer chain glycine homopeptides were observed, which was normally classified to nonclassical nucleation theory. This work provides insight into how the nucleation process evolves with increasing chain length and variable conformation, thereby offering a fundamental understanding of the critical peptide chain length for the classical nucleation theory and complex nucleation process for peptides.
为了探究链长和构象对肽成核的影响,已测定了甘氨酸同肽在不同温度下、不同过饱和度水平的纯水中的初级成核诱导时间。成核数据表明,较长的链会延长诱导时间,尤其是对于长度超过三个的链,成核会在数天内发生。相比之下,所有同肽的成核速率都随着过饱和度的增加而增加。在较低温度下,诱导时间和成核难度会增加。然而,对于三甘氨酸,在低温下会产生具有未折叠肽构象(pPII)的二水合物形式。这种二水合物形式的界面能和活化吉布斯自由能均低于高温时的,而诱导时间更长,这表明经典成核理论不适用于解释三甘氨酸二水合物的成核现象。此外,还观察到了较长链甘氨酸同肽的凝胶化和液-液分离现象,这通常归类于非经典成核理论。这项工作深入了解了成核过程如何随着链长增加和构象变化而演变,从而为经典成核理论的关键肽链长度和肽的复杂成核过程提供了基本认识。