The Dual Role of Choline O sulfate on Chemical Denaturation of Proteins and Amyloid Aggregation A Computational Study

dc.contributor.guidePaul, Sandip
dc.coverage.spatialChemistry
dc.creator.researcherPaul, Srijita
dc.date.accessioned2022-12-12T11:39:28Z
dc.date.available2022-12-12T11:39:28Z
dc.date.awarded2021
dc.date.completed2020
dc.date.registered2015
dc.description.abstractThis thesis represents the molecule choline-O-sulfate as a protecting osmolyte in the protein folding-unfolding process as well as a potent inhibitor in the field of peptide aggregation. The thesis is divided into seven chapters.Chapter 1 of the thesis includes a review of related experimental and theoretical works that exist in the literature together with the basic techniques of MD simulations. In Chapter 2, we have studied the synergistic behavior of urea-COS mixture through classical molecular dynamics simulation. Here we have studied all possible interactions between urea and COS present in a mixture to find out the mechanism of the counteraction of urea by COS against urea-induced denaturation of the protein. Chapter 3 deals with the direct application of COS as a protecting osmolyte in the protein folding-unfolding process. This chapter has been divided into two parts, Part A and Part B. Chapter 3A describes how COS nullifies the deleterious effects of urea on a 15 residue modeled peptide named S-peptide through classical molecular dynamics simulation. Chapter 3B includes the findings on the counteracting ability of COS against urea on a small globular protein called Trp-cage by an enhanced sampling method called Replica Exchange Molecular Dynamics (REMD) simulation. In the next chapter i.e. Chapter 4, we have discussed the unfolding of the terminal helices of the and#955;-repressor protein by an unconventional denaturant dodine and its stability in presence of COS. In Chapter 5, we have reported our research work on the inhibitory effects of COS in the aggregation of human islet amyloid polypeptide, responsible for Type-II diabetes mellitus (T2Dm). In Chapter 6, we have presented COS as a potent inhibitor in the self-association of Aand#946;16and#8722;22 peptide, associated with Alzheimer s disease. In the last chapter i.e., Chapter 7, we have summarized our overall findings to bring a concrete conclusion portraying COS as an efficient osmolyte as well as an inhibitor. Successful application of COS on two different kinds of pr
dc.description.noteNot Available
dc.format.accompanyingmaterialNone
dc.format.dimensionsNot Available
dc.format.extentNot Available
dc.identifier.urihttp://hdl.handle.net/10603/424873
dc.languageEnglish
dc.publisher.institutionDEPARTMENT OF CHEMISTRY
dc.publisher.placeGuwahati
dc.publisher.universityIndian Institute of Technology Guwahati
dc.relationNot Available
dc.rightsself
dc.source.universityUniversity
dc.subject.keywordChemistry
dc.subject.keywordChemistry Applied
dc.subject.keywordPhysical Sciences
dc.titleThe Dual Role of Choline O sulfate on Chemical Denaturation of Proteins and Amyloid Aggregation A Computational Study
dc.title.alternativeNot available
dc.type.degreePh.D.

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