TY - JOUR
T1 - Structural Insights Into TDP-43 and Effects of Post-translational Modifications
AU - François-Moutal, Liberty
AU - Perez-Miller, Samantha
AU - Scott, David D.
AU - Miranda, Victor G.
AU - Mollasalehi, Niloufar
AU - Khanna, May
N1 - Publisher Copyright:
© Copyright © 2019 François-Moutal, Perez-Miller, Scott, Miranda, Mollasalehi and Khanna.
PY - 2019/12/17
Y1 - 2019/12/17
N2 - Transactive response DNA binding protein (TDP-43) is a key player in neurodegenerative diseases. In this review, we have gathered and presented structural information on the different regions of TDP-43 with high resolution structures available. A thorough understanding of TDP-43 structure, effect of modifications, aggregation and sites of localization is necessary as we develop therapeutic strategies targeting TDP-43 for neurodegenerative diseases. We discuss how different domains as well as post-translational modification may influence TDP-43 overall structure, aggregation and droplet formation. The primary aim of the review is to utilize structural insights as we develop an understanding of the deleterious behavior of TDP-43 and highlight locations of established and proposed post-translation modifications. TDP-43 structure and effect on localization is paralleled by many RNA-binding proteins and this review serves as an example of how structure may be modulated by numerous compounding elements.
AB - Transactive response DNA binding protein (TDP-43) is a key player in neurodegenerative diseases. In this review, we have gathered and presented structural information on the different regions of TDP-43 with high resolution structures available. A thorough understanding of TDP-43 structure, effect of modifications, aggregation and sites of localization is necessary as we develop therapeutic strategies targeting TDP-43 for neurodegenerative diseases. We discuss how different domains as well as post-translational modification may influence TDP-43 overall structure, aggregation and droplet formation. The primary aim of the review is to utilize structural insights as we develop an understanding of the deleterious behavior of TDP-43 and highlight locations of established and proposed post-translation modifications. TDP-43 structure and effect on localization is paralleled by many RNA-binding proteins and this review serves as an example of how structure may be modulated by numerous compounding elements.
KW - RRM domain
KW - TDP-43 = TAR DNA–binding protein 43
KW - post-translational modification
KW - structure
KW - subdomains
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U2 - 10.3389/fnmol.2019.00301
DO - 10.3389/fnmol.2019.00301
M3 - Review article
AN - SCOPUS:85077355429
SN - 1662-5099
VL - 12
JO - Frontiers in Molecular Neuroscience
JF - Frontiers in Molecular Neuroscience
M1 - 301
ER -