Misfolded protein linked strategies toward biomarker development for neurodegenerative diseases

The progressive loss of structure and function of neurons causes various neurodegenerative diseases which need to be examined using measurable indicators, known as biomarkers. Proteins are the building blocks for the cell and are essential as they participate in many processes in the cells. When bio...

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Main Authors: Kumar, Sundramurthy, Karthikeyan, Narayanan, Mishra, Sachin, Padmanabhan, Parasuraman, Radda, George, Gulyás, Balázs
Other Authors: Lee Kong Chian School of Medicine (LKCMedicine)
Format: Journal Article
Language:English
Published: 2021
Subjects:
Online Access:https://hdl.handle.net/10356/151351
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author Kumar, Sundramurthy
Karthikeyan, Narayanan
Mishra, Sachin
Padmanabhan, Parasuraman
Radda, George
Gulyás, Balázs
author2 Lee Kong Chian School of Medicine (LKCMedicine)
author_facet Lee Kong Chian School of Medicine (LKCMedicine)
Kumar, Sundramurthy
Karthikeyan, Narayanan
Mishra, Sachin
Padmanabhan, Parasuraman
Radda, George
Gulyás, Balázs
author_sort Kumar, Sundramurthy
collection NTU
description The progressive loss of structure and function of neurons causes various neurodegenerative diseases which need to be examined using measurable indicators, known as biomarkers. Proteins are the building blocks for the cell and are essential as they participate in many processes in the cells. When biologically essential proteins are impaired, it leads to devastating consequences in humans and mammals among which the most prominent is neurodegenerative disease. Proteins conform to three-dimensional structures to enable their functions. Besides, some proteins have the tendency to form self-assembly structures. When these self-assembly proteins assume abnormal conformation, they accumulate and cause pathological conditions. The genetic and molecular origins of protein misfolding in association with their relationship with neurodegeneration and aging are being studied to better understand and develop treatments. Accumulations of these misfolded proteins form aggregates which is considered as the most prominent cause of many neurodegenerative diseases. This article reviews the misfolded proteins in various neurodegenerative diseases and analyzes the diverse aspects of protein misfolding as a potential agent of biomarkers with an approach for finding an inhibitor for misfolding.
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spelling ntu-10356/1513512021-06-22T09:41:25Z Misfolded protein linked strategies toward biomarker development for neurodegenerative diseases Kumar, Sundramurthy Karthikeyan, Narayanan Mishra, Sachin Padmanabhan, Parasuraman Radda, George Gulyás, Balázs Lee Kong Chian School of Medicine (LKCMedicine) Science::Medicine Misfolded Protein Neurodegenerative Diseases The progressive loss of structure and function of neurons causes various neurodegenerative diseases which need to be examined using measurable indicators, known as biomarkers. Proteins are the building blocks for the cell and are essential as they participate in many processes in the cells. When biologically essential proteins are impaired, it leads to devastating consequences in humans and mammals among which the most prominent is neurodegenerative disease. Proteins conform to three-dimensional structures to enable their functions. Besides, some proteins have the tendency to form self-assembly structures. When these self-assembly proteins assume abnormal conformation, they accumulate and cause pathological conditions. The genetic and molecular origins of protein misfolding in association with their relationship with neurodegeneration and aging are being studied to better understand and develop treatments. Accumulations of these misfolded proteins form aggregates which is considered as the most prominent cause of many neurodegenerative diseases. This article reviews the misfolded proteins in various neurodegenerative diseases and analyzes the diverse aspects of protein misfolding as a potential agent of biomarkers with an approach for finding an inhibitor for misfolding. Agency for Science, Technology and Research (A*STAR) Nanyang Technological University Author SK, PP, and BG like to acknowledge the support from Lee Kong Chian School of Medicine, Nanyang Technological University Start-Up Grant. KN likes to thank Institute of Bioengineering and Nanotechnology, Singapore, for funding. We would like to thank Ms. Suzanne Danley (Department of Orthopedics, West Virginia University) for editing the manuscript. 2021-06-22T09:41:25Z 2021-06-22T09:41:25Z 2019 Journal Article Kumar, S., Karthikeyan, N., Mishra, S., Padmanabhan, P., Radda, G. & Gulyás, B. (2019). Misfolded protein linked strategies toward biomarker development for neurodegenerative diseases. Molecular Neurobiology, 56(4), 2559-2578. https://dx.doi.org/10.1007/s12035-018-1232-4 0893-7648 0000-0001-5136-2296 https://hdl.handle.net/10356/151351 10.1007/s12035-018-1232-4 30043261 2-s2.0-85050638955 4 56 2559 2578 en Molecular Neurobiology © 2018 Springer Science Business Media, LLC, part of Springer Nature. All rights reserved.
spellingShingle Science::Medicine
Misfolded Protein
Neurodegenerative Diseases
Kumar, Sundramurthy
Karthikeyan, Narayanan
Mishra, Sachin
Padmanabhan, Parasuraman
Radda, George
Gulyás, Balázs
Misfolded protein linked strategies toward biomarker development for neurodegenerative diseases
title Misfolded protein linked strategies toward biomarker development for neurodegenerative diseases
title_full Misfolded protein linked strategies toward biomarker development for neurodegenerative diseases
title_fullStr Misfolded protein linked strategies toward biomarker development for neurodegenerative diseases
title_full_unstemmed Misfolded protein linked strategies toward biomarker development for neurodegenerative diseases
title_short Misfolded protein linked strategies toward biomarker development for neurodegenerative diseases
title_sort misfolded protein linked strategies toward biomarker development for neurodegenerative diseases
topic Science::Medicine
Misfolded Protein
Neurodegenerative Diseases
url https://hdl.handle.net/10356/151351
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