Antibody toolkit to investigate eEF1A methylation dynamics in mRNA translation elongation
Year: 2023
Type: article
Abstract: Protein synthesis is a fundamental step in gene expression, with modulation of mRNA translation at the elongation step emerging as an important regulatory node in shaping cellular proteomes. In this context, five distinct lysine methylation events on eukaryotic elongation factor 1A (eEF1A), a fundamental nonribosomal elongation factor, are proposed to influence mRNA translation elongation dynamics. However, a lack of affinity tools has hindered progress in fully understanding how eEF1A lysine methylation impacts protein synthesis. Here we develop and characterize a suite of selective antibodies to investigate eEF1A methylation and provide evidence that methylation levels decline in aged tissue. Determination of the methyl state and stoichiometry on eEF1A in various cell lines by mass spectrometry shows modest cell-to-cell variability. We also find by Western blot analysis that knockdown of individual eEF1A-specific lysine methyltransferases leads to depletion of the cognate lysine methylation event and indicates active crosstalk between different sites. Further, we find that the antibodies are specific in immunohistochemistry applications. Finally, application of the antibody toolkit suggests that several eEF1A methylation events decrease in aged muscle tissue. Together, our study provides a roadmap for leveraging methyl state and sequence-selective antibody reagents to accelerate discovery of eEF1A methylation-related functions and suggests a role for eEF1A methylation, via protein synthesis regulation, in aging biology.
Source: Journal of Biological Chemistry
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,800
Funders: U.S. Department of Defense, U.S. Department of Veterans Affairs, Cancer Prevention and Research Institute of Texas, National Institutes of Health, National Institute on Aging, National Cancer Institute, National Institute of General Medical Sciences, Stanford Cancer Institute, DOD Peer Reviewed Cancer Research Program
Awards: G202637879, Role of the METTL13 Lysine Methyltransferase in Signaling and Cancer, G2439014945, G2558943394, Identification of oncogenic mechanisms driving lung squamous cell carcinoma development and progression, G3183773579, Cellular and Molecular Biology Training Program, G4639202757, Role of the candidate protein methyltransferase METTL18 in cancer biology, Recruitment of First-Time, Tenure-Track Faculty Members, G7480755245, Role of SETD5 in Chromatin Regulation and Tumorigenesis, G7735735615, G8085314913, G9000264810, Role of NSD3 in regulation of cancer pathogenesis, Therapeutic Targeting of NSD2 in Lung Adenocarcinoma, Training in Basic Research on Aging and Age-Related Disease
OpenAlex ID: W4366748258
