{"title":"Conformational Dynamics of Post-Translational-Modified α-Synuclein\u0000(pY39 and pS87) and its Interaction with Lipid Membrane","authors":"D. Das, V. S. Mattaparthi","doi":"10.2174/0122115501310995240522064640","DOIUrl":"https://doi.org/10.2174/0122115501310995240522064640","url":null,"abstract":"\u0000\u0000The biological function of α-Synuclein (α-Syn), which includes controlling\u0000synaptic vesicles, is regulated by phosphorylation at the Tyrosine 39 (pY39) residue. This\u0000function can be important for both normal and aberrant functions, and it relies on the interaction\u0000of α-Syn with the lipid membrane. pY39 α-Syn is found to form morphologically distinct fibrils\u0000relative to wild-type (WT) α-Syn and shows less affinity to negatively charged vesicles. Also, the\u0000phosphorylation at position Serine 87 (pS87) is increased in synucleinopathies, which inhibits α-\u0000Syn oligomerization and affects the interaction between α-Syn and the membrane.\u0000\u0000\u0000\u0000This work aimed to study the effects of post-translation modifications of α-Syn (pY39\u0000and pS87) using all-atom Molecular Dynamics (MD) simulation\u0000\u0000\u0000\u0000In this computational study, we used all-atom MD simulations to investigate the effects\u0000of phosphorylation (pY39 and pS87) on protein-membrane interaction. The MD trajectories obtained\u0000were analyzed, and secondary structural content was calculated using YASARA software\u0000to perform a salt-bridge interaction study. Also, Principal component analysis was performed to\u0000analyze the secondary minima and global minima of the phosphorylated proteins.\u0000\u0000\u0000\u0000From the MD study, we observed that phosphorylation at the Tyr 39 position in α-Syn\u0000has a marked effect on its interaction with the lipid membrane. The conformational snapshots of\u0000α-Syn obtained showed a high degree of fluctuations in the N-terminal region that disrupts the helix-\u00002 binding region. The secondary structures of pS87 α-Syn were found to be retained and influence\u0000the NAC region to immerse into the membrane while inhibiting the potential to interact with\u0000other neighbouring molecules. Moreover, it was observed that in the case of pY39 α-Syn as opposed\u0000to pS87 α-Syn, there were larger energy disparities between the local and global minima of\u0000the overall structure.\u0000\u0000\u0000\u0000Therefore, disruption of the helix-2 binding region may affect the binding to the lipid\u0000membrane and take over interaction with other proteins or vesicles. In the case of pS87 α-Syn, the\u0000structure showed higher stability, but the NAC domain was found to emerge out of the membrane.\u0000","PeriodicalId":516136,"journal":{"name":"Current Biotechnology","volume":"252 6‐8","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141386654","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}