Effect of Polymer Conjugation Site on Stability and Self-Assembly of Coiled Coils

被引:12
作者
Hamed E. [1 ]
Ma D. [1 ]
Keten S. [1 ]
机构
[1] Department of Civil and Environmental Engineering and Mechanical Engineering, Northwestern University, Evanston, 60208, IL
关键词
Coarse-grained simulation; Coiled coils; Polymer conjugation; Self-assembly; Stability;
D O I
10.1007/s12668-015-0172-y
中图分类号
学科分类号
摘要
Conjugation of proteins with polymers has emerged as a new design technique to produce hybrid block copolymers with tailored hierarchical structures and desirable functionalities as well as greater stability. However, due to the sequence and chemistry dependence of the conjugation effects, it remains challenging to understand the overall effect of the location of polymer conjugation on supramolecular organization. As a step toward addressing this issue, here, we report coarse-grained molecular dynamics simulations of the supramolecular organization of coiled coil assemblies with terminal and side-chain conjugated alpha-helices. Our simulations indicate that helicity and thermal stability are preserved for both side and end polymer conjugation, but the steric hindrance by polymer chains influences the aggregation patterns of coiled coils in different ways, depending on the conjugation location. The aggregation number of assembled clusters decreases upon polymer conjugation, and this effect is more pronounced for side conjugation compared to end conjugation. Our results explain recent experimental findings on peptide-polymer conjugates and lay the groundwork for the design of protein assemblies with enhanced thermomechanical stability and controlled aggregation behavior in different environmental conditions. © 2015, Springer Science+Business Media New York.
引用
收藏
页码:140 / 149
页数:9
相关论文
共 45 条
[1]  
Eckert D.M., Kim P.S., Mechanisms of viral membrane fusion and its inhibition, Annual Review of Biochemistry, 70, pp. 777-810, (2001)
[2]  
Hurst H.C., Transcription factors 1: bZIP proteins, Protein Profile, 2, 2, pp. 101-168, (1995)
[3]  
Herrmann H., Et al., The intermediate filament protein consensus motif of helix 2B: its atomic structure and contribution to assembly, Journal of Molecular Biology, 298, pp. 817-832, (2000)
[4]  
Siegert R., Et al., Structure of the molecular chaperone prefoldin: unique interaction of multiple coiled coil tentacles with unfolded proteins, Cell, 103, 4, pp. 621-632, (2000)
[5]  
Mosesson M.W., Siebenlist K.R., Meh D.A., The structure and biological features of fibrinogen and fibrin, Annals of the New York Academy of Sciences, 936, pp. 11-30, (2001)
[6]  
Wang Y., Gao R., Lynn D.G., Ratcheting up vir gene expression in Agrobacterium tumefaciens: coiled coils in histidine kinase signal transduction, ChemBioChem, 3, pp. 311-317, (2002)
[7]  
Berwick M.R., Et al., De novo design of Ln(III) coiled coils for imaging applications, Journal of the American Chemical Society, 136, pp. 1166-1169, (2014)
[8]  
Chao H.M., Et al., Use of a heterodimeric coiled-coil system for biosensor application and affinity purification, Journal of Chromatography B, 715, 1, pp. 307-329, (1998)
[9]  
Jing P., Et al., Self-assembling peptide-polymer hydrogels designed from the coiled coil region of fibrin, Biomacromolecules, 9, pp. 2438-2446, (2008)
[10]  
Petka W.A., Et al., Reversible hydrogels from self-assembling artificial proteins, Science, 281, 5375, pp. 389-392, (1998)