The small membrane protein YohP induces membrane depolarization and ppGpp accumulation in Escherichia coli.

Small membrane proteins represent an abundant and ubiquitous class of proteins that are often up-regulated when cells encounter unfavorable conditions, yet details about their exact function are largely missing. In bacteria, these proteins consist of typically less than 50 amino acids and contain a single transmembrane domain, but lack any detectable catalytic activity. Thus, the benefit of producing these proteins during stress conditions is unknown. In the current study we used a multidisciplinary approach to determine the function of the 27 amino acid long protein YohP in E. coli. Our proteomics approach revealed that YohP production leads to an up-regulation of proteins involved in membrane protection and to a down-regulation of many enzymes involved in key metabolic processes, such as nucleotide biosynthesis. Further biochemical characterizations revealed increased cardiolipin content in the membrane, a partial dissipation of the membrane potential and reduced membrane fluidity in YohP-containing membranes. Finally, our data show that YohP production induces the stringent response and leads to elevated levels of (p)ppGpp. Overall, our data indicate that the YohP-induced proteome and membrane changes initiate a state of metabolic silencing that protects E. coli against stress and helps to conserve cellular resources.