Recent advances in genome-scale modeling of proteome allocation

Abstract Genome-scale models (GEMs) have been expanded to compute both the metabolic and proteomic states of a cell in different conditions. These multi-scale models called genome-scale models of metabolism and macromolecular expression (ME-models) expand the scope of GEMs and provide greater predictive abilities, and therefore are being increasingly used in systems understanding of microbial biology. In this review, we describe ME-models, their advantages, and computational advances. We then describe extensions of ME-models to model stress response, and a related human red blood cell model that integrate metabolism and macromolecular mechanisms. Finally, we discuss how ME-models were recently used to explain resource allocation tradeoffs for microbial growth in adaptively evolved strains, in synthetic communities, and under stress.