Conformational stability of PCID2 upon DSS1 binding with molecular dynamics simulation

Verfasser / Beitragende:
[Qianjun Liu, Guodong Hu, Zanxia Cao, Jihua Wang, Haifeng Chen]
Ort, Verlag, Jahr:
2015
Enthalten in:
Journal of Molecular Modeling, 21/5(2015-05-01), 1-9
Format:
Artikel (online)
ID: 605513376
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024 7 0 |a 10.1007/s00894-015-2664-7  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s00894-015-2664-7 
245 0 0 |a Conformational stability of PCID2 upon DSS1 binding with molecular dynamics simulation  |h [Elektronische Daten]  |c [Qianjun Liu, Guodong Hu, Zanxia Cao, Jihua Wang, Haifeng Chen] 
520 3 |a DSS1 is a small acidic intrinsically disordered protein (IDP) that can fold upon binding with PCID2 TREX-2. The resulting complex plays a key role in mRNA export. However, the binding mechanism between DSS1 and PCID2 is unsolved. Here, three independent 500-ns molecular dynamics (MD) simulations were performed to study the DSS1-PCID2 binding mechanism by comparing apo-PCID2 and bound PCID2. The results show that the conformational variation of bound PCID2 is smaller than that of apo-PCID2, especially in the binding domain of two helices (helix IV and VIII). The probability of coil formation between helix III and helix IV of bound PCID2 increases, and a short anti-parallel β-sheet forms upon DSS1 binding. The decomposition of binding free energy into protein and residue pairs suggests that electrostatic and hydrophobic interactions play key roles in the recognition between DSS1 and PCID2. There is a hydrophobic core of seven residues in DSS1 favorable to the binding of PCID2. These analytical methods can be used to reveal the recognition mechanisms of other IDPs and their partners. Figure Differences of second structure of PCID2 in bound and unbound states. The interaction surface between the helix VIII of PCID2 and helix of DSS1 
540 |a Springer-Verlag Berlin Heidelberg, 2015 
690 7 |a PCID2 protein  |2 nationallicence 
690 7 |a Molecular dynamics simulation  |2 nationallicence 
690 7 |a Conformational changes  |2 nationallicence 
690 7 |a Binding free energy  |2 nationallicence 
700 1 |a Liu  |D Qianjun  |u Shandong Provincial Key Laboratory of Functional Macromolecular Biophysics, College of Physics and Electronic Information, Dezhou University, 253023, Dezhou, China  |4 aut 
700 1 |a Hu  |D Guodong  |u Shandong Provincial Key Laboratory of Functional Macromolecular Biophysics, College of Physics and Electronic Information, Dezhou University, 253023, Dezhou, China  |4 aut 
700 1 |a Cao  |D Zanxia  |u Shandong Provincial Key Laboratory of Functional Macromolecular Biophysics, College of Physics and Electronic Information, Dezhou University, 253023, Dezhou, China  |4 aut 
700 1 |a Wang  |D Jihua  |u Shandong Provincial Key Laboratory of Functional Macromolecular Biophysics, College of Physics and Electronic Information, Dezhou University, 253023, Dezhou, China  |4 aut 
700 1 |a Chen  |D Haifeng  |u State Key Laboratory of Microbial Metabolism, Department of Bioinformatics and Biostatistics, College of Life Sciences and Biotechnology, Shanghai Jiaotong University, 200240, Shanghai, China  |4 aut 
773 0 |t Journal of Molecular Modeling  |d Springer Berlin Heidelberg  |g 21/5(2015-05-01), 1-9  |x 1610-2940  |q 21:5<1  |1 2015  |2 21  |o 894 
856 4 0 |u https://doi.org/10.1007/s00894-015-2664-7  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s00894-015-2664-7  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Liu  |D Qianjun  |u Shandong Provincial Key Laboratory of Functional Macromolecular Biophysics, College of Physics and Electronic Information, Dezhou University, 253023, Dezhou, China  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Hu  |D Guodong  |u Shandong Provincial Key Laboratory of Functional Macromolecular Biophysics, College of Physics and Electronic Information, Dezhou University, 253023, Dezhou, China  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Cao  |D Zanxia  |u Shandong Provincial Key Laboratory of Functional Macromolecular Biophysics, College of Physics and Electronic Information, Dezhou University, 253023, Dezhou, China  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Wang  |D Jihua  |u Shandong Provincial Key Laboratory of Functional Macromolecular Biophysics, College of Physics and Electronic Information, Dezhou University, 253023, Dezhou, China  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Chen  |D Haifeng  |u State Key Laboratory of Microbial Metabolism, Department of Bioinformatics and Biostatistics, College of Life Sciences and Biotechnology, Shanghai Jiaotong University, 200240, Shanghai, China  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Journal of Molecular Modeling  |d Springer Berlin Heidelberg  |g 21/5(2015-05-01), 1-9  |x 1610-2940  |q 21:5<1  |1 2015  |2 21  |o 894