Understanding proteins folding mechanism : precursors and fingerprints.

This thesis aims to understand the mechanism of protein folding from the statistical viewpoint by using the measure of Pearson's correlation coefficient(PCC). Protein folding is one of the most actively researched field, yet its mechanism is still a mystery to scientists. Understanding the mech...

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Main Author: Chua, Khi Pin.
Other Authors: Cheong Siew Ann
Format: Final Year Project
Language:English
Published: 2013
Subjects:
Online Access:http://hdl.handle.net/10356/52866
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-528662023-02-28T23:15:06Z Understanding proteins folding mechanism : precursors and fingerprints. Chua, Khi Pin. Cheong Siew Ann School of Physical and Mathematical Sciences DRNTU::Science::Biological sciences::Biophysics This thesis aims to understand the mechanism of protein folding from the statistical viewpoint by using the measure of Pearson's correlation coefficient(PCC). Protein folding is one of the most actively researched field, yet its mechanism is still a mystery to scientists. Understanding the mechanism is vital to the medical field as protein misfolding is known to be the cause of various diseases like Parkinson and Alzheimer disease. Besides, being able to pinpoint the protein folding pathway will provide a significant breakthrough in the field of medical drug design. The correlations between angles of residues (which is defined later) are calculated to study the dynamics between the residues. Three simulated polyalanine peptides that folded into fi-helices are studied, namely Q, K and D that only differ among themselves in two substituted residues in each amino acid sequence. D has the lowest fi- helical content among the three peptides and is considered to be only partially folded. We look for precursors preceding the folding process and fingerprints in the correlation time series. It is found that there are a number of common precursors between the three pep- tides. One important precursor involving the substituted residue is present in both protein Q and K, but notably absent in D. The precursor could be the key to the partial folding attempt in D. PCC method also captures the fingerprints characterizing the folded states of the peptides. Cross checking the time where the fingerprints start appearing with the pictures of molecules drawn in VMD(Visual Molecular Dynamics) confirms our finding. We can also see interesting patterns in the trajectory and fluctuation of the cosine of angles between residues involved in the important precursor mentioned above. The patterns imply phase transitions surrounding the period of the precursors. Bachelor of Science in Physics 2013-05-28T08:45:00Z 2013-05-28T08:45:00Z 2013 2013 Final Year Project (FYP) http://hdl.handle.net/10356/52866 en 58 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Science::Biological sciences::Biophysics
spellingShingle DRNTU::Science::Biological sciences::Biophysics
Chua, Khi Pin.
Understanding proteins folding mechanism : precursors and fingerprints.
description This thesis aims to understand the mechanism of protein folding from the statistical viewpoint by using the measure of Pearson's correlation coefficient(PCC). Protein folding is one of the most actively researched field, yet its mechanism is still a mystery to scientists. Understanding the mechanism is vital to the medical field as protein misfolding is known to be the cause of various diseases like Parkinson and Alzheimer disease. Besides, being able to pinpoint the protein folding pathway will provide a significant breakthrough in the field of medical drug design. The correlations between angles of residues (which is defined later) are calculated to study the dynamics between the residues. Three simulated polyalanine peptides that folded into fi-helices are studied, namely Q, K and D that only differ among themselves in two substituted residues in each amino acid sequence. D has the lowest fi- helical content among the three peptides and is considered to be only partially folded. We look for precursors preceding the folding process and fingerprints in the correlation time series. It is found that there are a number of common precursors between the three pep- tides. One important precursor involving the substituted residue is present in both protein Q and K, but notably absent in D. The precursor could be the key to the partial folding attempt in D. PCC method also captures the fingerprints characterizing the folded states of the peptides. Cross checking the time where the fingerprints start appearing with the pictures of molecules drawn in VMD(Visual Molecular Dynamics) confirms our finding. We can also see interesting patterns in the trajectory and fluctuation of the cosine of angles between residues involved in the important precursor mentioned above. The patterns imply phase transitions surrounding the period of the precursors.
author2 Cheong Siew Ann
author_facet Cheong Siew Ann
Chua, Khi Pin.
format Final Year Project
author Chua, Khi Pin.
author_sort Chua, Khi Pin.
title Understanding proteins folding mechanism : precursors and fingerprints.
title_short Understanding proteins folding mechanism : precursors and fingerprints.
title_full Understanding proteins folding mechanism : precursors and fingerprints.
title_fullStr Understanding proteins folding mechanism : precursors and fingerprints.
title_full_unstemmed Understanding proteins folding mechanism : precursors and fingerprints.
title_sort understanding proteins folding mechanism : precursors and fingerprints.
publishDate 2013
url http://hdl.handle.net/10356/52866
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