Publications by authors named "Mara Leite"

Establishing the first human presence on Mars will be the most technically challenging undertaking yet in the exploration beyond our planet. The remoteness of Mars from Earth, the inhospitable surface conditions including low atmospheric pressure and cold temperatures, and the need for basic resources including water, pose a formidable challenge to this endeavour. The intersection of multiple disciplines will be required to provide solutions for temporary and eventually permanent Martian habitation.

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Article Synopsis
  • The study focuses on strain FS406-22, a heat-loving methanogen that can fix nitrogen using a minimal set of genes, including just four main structural genes and a homolog found elsewhere in its genome.
  • The absence of a key gene necessary for forming the nitrogenase cofactor in related organisms, coupled with the discovery of novel proteins, raises questions about how nitrogen fixation evolved in FS406-22.
  • Researchers developed genetic tools to manipulate FS406-22, demonstrating that the deletion of one gene affected growth and suggesting a cooperative role with another gene in nitrogen fixation processes.
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The outer membranes of Gram-negative bacteria and mitochondria contain proteins with a distinct β-barrel tertiary structure that could function as a molecular pattern recognized by the innate immune system. Here, we report that purified outer membrane proteins (OMPs) from different bacterial and mitochondrial sources triggered the induction of autophagy-related endosomal acidification, LC3B lipidation, and p62 degradation. Furthermore, OMPs reduced the phosphorylation and therefore activation of the multiprotein complex mTORC2 and its substrate Akt in macrophages and epithelial cells.

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Mutations in genes encoding autophagy proteins have been associated with human autoimmune diseases, suggesting that diversity in autophagy responses could be associated with disease susceptibility or severity. A cellular genome-wide association study (GWAS) screen was performed to explore normal human diversity in responses to rapamycin, a microbial product that induces autophagy. Cells from several human populations demonstrated variability in expression of a cell surface receptor, CD244 (SlamF4, 2B4), that correlated with changes in rapamycin-induced autophagy.

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