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Reversible folding/unfolding of smallα-helix in explicit solvent investigated by ABEEMσπ/MM 被引量:3
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作者 LIU Cui YANG ZhongZhi 《Science China Chemistry》 SCIE EI CAS 2009年第11期1917-1924,共8页
We have performed molecular dynamics simulations on the reversible folding/unfolding of smallα-helix(short Ala based peptide Ala5)in explicit water solvent in terms of ABEEMσπ/MM.A dynamics analysis shows that the... We have performed molecular dynamics simulations on the reversible folding/unfolding of smallα-helix(short Ala based peptide Ala5)in explicit water solvent in terms of ABEEMσπ/MM.A dynamics analysis shows that theα-helical turn can be preserved up to a period of about 2 ns at 300 K,which supports the conclusions of Margulis et al.The time trajectory of the root mean square deviation between the heavy atoms of the backbone and the helical reference structure indicate that"helix melting and formation occurs rapidly on a time scale of 0.1 ns at 300 K"is not a felicitous conclusion.We first quantificationally concluded that the helix nucleation can maintain 2 ns,1―1.5 ns and 0.8 ns for Ala5 at 300 K,400 K and 500 K,respectively.Furthermore,increasing temperature dose not alter the pathway of folding/unfolding,but change the rate.An analysis of structures in a"transition-state ensemble"shows that helix-to-coil transitions occurs predominantly through breaking of hydrogen bonds at the helix ends(92%),particularly at the C-terminus(50%).Hydrogen bonds'breaking and formation occurs on a time scale of 0.1 ns. 展开更多
关键词 reversible folding/unfolding of protein Ala5 temperature hydrogen bond
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