Docking and molecular dynamics simulations of the Fyn‐SH3 domain with free and phospholipid bilayer‐associated 18.5‐kDa myelin basic protein (MBP)—Insights into a noncanonical and fuzzy interaction. Issue 7 (10th May 2017)

• Record Type: Journal Article
• Authors: Bessonov, Kyrylo; Vassall, Kenrick A.; Harauz, George
• Is Part Of: Proteins. Volume 85:Issue 7(2017)
• Page Start: 1336
• Page End: 1350
• Publication Date: 2017-05-10
• Subjects: amphipathic α‐helix -- poly‐proline type II (PPII) -- Fyn‐SH3 -- intrinsically disordered protein (IDP) -- myelin basic protein (MBP) -- molecular dynamics (MD) simulations -- molecular recognition fragment (MoRF) -- GROMACS; Proteins -- Periodicals; Proteins -- Periodicals; 572.6
• DOI: 10.1002/prot.25295
• Languages: English
• ISSNs: 0887-3585

Abstract

ABSTRACT: The molecular details of the association between the human Fyn‐SH3 domain, and the fragment of 18.5‐kDa myelin basic protein (MBP) spanning residues S38–S107 (denoted as xα2‐peptide, murine sequence numbering), were studied in silico via docking and molecular dynamics over 50‐ns trajectories. The results show that interaction between the two proteins is energetically favorable and heavily dependent on the MBP proline‐rich region (P93‐P98) in both aqueous and membrane environments. In aqueous conditions, the xα2‐peptide/Fyn‐SH3 complex adopts a "sandwich""‐like structure. In the membrane context, the xα2‐peptide interacts with the Fyn‐SH3 domain via the proline‐rich region and the β‐sheets of Fyn‐SH3, with the latter wrapping around the proline‐rich region in a form of a clip. Moreover, the simulations corroborate prior experimental evidence of the importance of upstream segments beyond the canonical SH3‐ligand. This study thus provides a more‐detailed glimpse into the context‐dependent interaction dynamics and importance of the β‐sheets in Fyn‐SH3 and proline‐rich region of MBP. Proteins 2017; 85:1336–1350. © 2017 Wiley Periodicals, Inc.