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Published on: February 17, 2023
The N-terminus of TDP-43 promotes its oligomerization and enhances DNA binding affinity
Chung-ke Chang1, Tzong-Huah Wu, Chu-Ya Wu
1Institute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan.
Abstract:
TDP-43 is a DNA/RNA-binding protein associated with different neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD-U). Here, the structural and physical properties of the N-terminus on TDP-43 have been carefully characterized through a combination of nuclear magnetic resonance (NMR), circular dichroism (CD) and fluorescence anisotropy studies. We demonstrate for the first time the importance of the N-terminus in promoting TDP-43 oligomerization and enhancing its DNA-binding affinity. An unidentified structural domain in the N-terminus is also disclosed. Our findings provide insights into the N-terminal domain function of TDP-43.
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