Predicting Collagen Triple Helix Stability through Additive Effects of Terminal Residues and Caps

被引:11
|
作者
Fiala, Tomas [1 ]
Barros, Emilia P. [2 ]
Heeb, Rahel [1 ]
Riniker, Sereina [2 ]
Wennemers, Helma [1 ]
机构
[1] Swiss Fed Inst Technol, Lab Organ Chem, Vladimir Prelog Weg 3, CH-8093 Zurich, Switzerland
[2] Swiss Fed Inst Technol, Lab Phys Chem, Vladimir Prelog Weg 2, CH-8093 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
Collagen; n?pi* Interaction; Peptides; Terminal Capping Group; Thermal Stability; CONFORMATIONAL STABILITY; CRYSTAL-STRUCTURE; MODEL PEPTIDES; CYSTINE KNOTS; TRIMERS; PROLINE;
D O I
10.1002/anie.202214728
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Collagen model peptides (CMPs) consisting of proline-(2S,4R)-hydroxyproline-glycine (POG) repeats have provided a breadth of knowledge of the triple helical structure of collagen, the most abundant protein in mammals. Predictive tools for triple helix stability have, however, lagged behind since the effect of CMPs with different frames ([POG](n), [OGP](n), or [GPO](n)) and capped or uncapped termini have so far been underestimated. Here, we elucidated the impact of the frame, terminal functional group and its charge on the stability of collagen triple helices. Combined experimental and theoretical studies with frame-shifted, capped and uncapped CMPs revealed that electrostatic interactions, strand preorganization, interstrand H-bonding, and steric repulsion at the termini contribute to triple helix stability. We show that these individual contributions are additive and allow for the prediction of the melting temperatures of CMP trimers.
引用
收藏
页数:10
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