Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/371011
Title: Bioactive Macrocyclic Cysteine rich Peptides Insights on Sequence Structure and Application of Cyclotides
Researcher: Kalmankar, Neha Vijay
Guide(s): Venkatesan, Radhika
Keywords: and#946;-amyloid inhibitors
bioactive peptides
Biology and Biochemistry
Cell Biology
cyclotides
disulfide-rich peptide modelling
Life Sciences
proteomics
transcriptomics
University: Institute of Trans-disciplinary Health Science and Technology
Completed Date: 2021
Abstract: Cyclotides are a unique class of gene-encoded, ribosomally synthesized, macrocyclic peptides (26-37 residues) produced in several plant species. They form a cyclic cystine knot (CCK) motif comprising of six disulfide bonds and circular backbone, and can be divided into two main subfamilies i.e. Möbius newlineand Bracelet, with Möbius cyclotides containing a cis-proline residue in the loop 5 region. newlineThe transcriptome assembly of Clitoria ternatea was performed to facilitate gene mining of cyclotide precursors arising in four tissues (pod, stem, leaf and flower). This resulted in the identification of 71 newlineprecursor genes, of which 26 are novel cyclotide sequences. Differential expression analysis revealed that numerous cyclotide genes were differentially expressed across the tissues. Moreover, we have also newlineproposed a model of cyclotide biosynthesis, wherein we followed the presence and expression of several oxidative folding and processing enzymes. Additionally, an assortment of cyclotides was detected across five tissues using proteomics method. Notable variations in LC-MS/MS product ion newlinedistributions were observed in cyclotides belonging to the two structural subfamilies based on the number and positions of prolines. Distinct MS/MS patterns determined by Xxx-Pro bond fragmentation of prototypical cyclotides was used as a diagnostic to rapidly sequence two novel cyclotides, ctr pep 30 and ctr pep 43. newlineFurthermore, our in-house disulfide bond database - DSDBASE2.0 was updated to include the latest PDB entries (January 2021 release) and multiple tools were incorporated for structure prediction of disulfide-rich peptides (http://caps.ncbs.res.in/dsdbase2). It is now possible to also obtain three dimensional models of disulfide-rich proteins using an independent algorithm - RANMOD. Finally, we cyclotides ability as an inhibitor of and#946;-amyloid (Aand#946;) fibrils was investigated and demonstrated using an animal model of Alzheimer s disease.
Pagination: 
URI: http://hdl.handle.net/10603/371011
Appears in Departments:Centre for Functional Genomics & Bio-informatics

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