A systematic mutational framework for studying oxidative phosphorylation-related proteins
Author:
Funder
U.S. Department of Health ; Human Services | NIH | National Institute of General Medical Sciences
U.S. Department of Health ; Human Services | NIH | National Institute on Aging
Publisher
Springer Science and Business Media LLC
Link
https://www.nature.com/articles/s42255-024-01042-7.pdf
Reference4 articles.
1. Sung, A. Y., Floyd, B. J. & Pagliarini, D. J. Systems biochemistry approaches to defining mitochondrial protein function. Cell Metab. 31, 669–678 (2020). A review that covers recent advances and approaches in characterizing the functions of mitochondrial proteins.
2. Schon, K. R., Ratnaike, T., Ameele, J., van den, Horvath, R. & Chinnery, P. F. Mitochondrial diseases: a diagnostic revolution. Trends Genet. 36, 702–717 (2020). A review that discusses diagnostic and therapeutic challenges of mitochondrial diseases.
3. Formosa, L. E., Dibley, M. G., Stroud, D. A. & Ryan, M. T. Building a complex complex: assembly of mitochondrial respiratory chain complex I. Semin. Cell Dev. Biol. 76, 154–162 (2018). A review that summarizes the current understanding of CI assembly.
4. Fowler, D. M. & Fields, S. Deep mutational scanning: a new style of protein science. Nat. Methods 11, 801–807 (2014). A review that provides an overview of DMS.
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