Simultaneous display of functional ligands on protein nanocage

The main objective of this project is to improve upon the current treatment of melasma by targeting melanocytes. This would be done by having a treatment that is both penetrative and specific. This novel approach is done by conjugating E2 protein cage together with space peptides to alpha peptide. S...

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Main Author: Nurul Syuhadah Johari
Other Authors: Lim Sierin
Format: Final Year Project
Language:English
Published: 2016
Subjects:
Online Access:http://hdl.handle.net/10356/68432
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-684322023-03-03T15:32:46Z Simultaneous display of functional ligands on protein nanocage Nurul Syuhadah Johari Lim Sierin School of Chemical and Biomedical Engineering Sathya Bashkar Moorthy DRNTU::Engineering The main objective of this project is to improve upon the current treatment of melasma by targeting melanocytes. This would be done by having a treatment that is both penetrative and specific. This novel approach is done by conjugating E2 protein cage together with space peptides to alpha peptide. Space peptides and alpha peptides are what make this treatment specific and penetrative, as it will target the melanocytes and the dermis and epidermis itself. The conjugation method that was used was the EDC-NHS Conjugation method. This particular conjugation method has varying critical parameters that need to be optimized in order for the EDC-NHS conjugation to be successful. The critical parameters include concentration of protein, pH and also molar ratio between the two proteins. After the conjugation is done, to know whether a conjugation is successful, either mass spectrometry and/or SDS-Page is done. When there is a conjugation, there will be a shift in the weight of the protein to show that it has successfully attached to the protein cage. Bachelor of Engineering (Chemical and Biomolecular Engineering) 2016-05-26T02:12:35Z 2016-05-26T02:12:35Z 2016 Final Year Project (FYP) http://hdl.handle.net/10356/68432 en Nanyang Technological University 46 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::Engineering
spellingShingle DRNTU::Engineering
Nurul Syuhadah Johari
Simultaneous display of functional ligands on protein nanocage
description The main objective of this project is to improve upon the current treatment of melasma by targeting melanocytes. This would be done by having a treatment that is both penetrative and specific. This novel approach is done by conjugating E2 protein cage together with space peptides to alpha peptide. Space peptides and alpha peptides are what make this treatment specific and penetrative, as it will target the melanocytes and the dermis and epidermis itself. The conjugation method that was used was the EDC-NHS Conjugation method. This particular conjugation method has varying critical parameters that need to be optimized in order for the EDC-NHS conjugation to be successful. The critical parameters include concentration of protein, pH and also molar ratio between the two proteins. After the conjugation is done, to know whether a conjugation is successful, either mass spectrometry and/or SDS-Page is done. When there is a conjugation, there will be a shift in the weight of the protein to show that it has successfully attached to the protein cage.
author2 Lim Sierin
author_facet Lim Sierin
Nurul Syuhadah Johari
format Final Year Project
author Nurul Syuhadah Johari
author_sort Nurul Syuhadah Johari
title Simultaneous display of functional ligands on protein nanocage
title_short Simultaneous display of functional ligands on protein nanocage
title_full Simultaneous display of functional ligands on protein nanocage
title_fullStr Simultaneous display of functional ligands on protein nanocage
title_full_unstemmed Simultaneous display of functional ligands on protein nanocage
title_sort simultaneous display of functional ligands on protein nanocage
publishDate 2016
url http://hdl.handle.net/10356/68432
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