Applications are sought for a full-time Assistant Project Scientist position in the Samelson Lab. The successful candidate will combine extensive chemoproteomics experience, protein expression, mammalian tissue culture, spectroscopy, and bioinformatics skills to understand iron and iron-chaperone distribution, function, and disease-relevance in human cell culture models of neurodegenerative diseases. The Samelson Lab is looking to understand how metals, especially those related to electron transport or iron homeostasis, affect disease-relevant phenotypes, such as protein aggregation, mitochondrial dysfunction, DNA damage, and lysosomal dysfunction. We are looking to combine mass-spectrometry-based methods for assessing iron occupancy in vivo with proteome-wide iron-chaperone interactome maps and genetic modifiers of these processes using CRISPR-screening.