Although mycoplasmas have small genomes, many of them, including the HIV-associated opportunist , construct a polar attachment organelle (AO) that is used for both adherence to host cells and gliding motility. However, the irregular phylogenetic distribution of similar structures within the mycoplasmas, as well as compositional and ultrastructural differences among these AOs, suggests that AOs have arisen several times through convergent evolution. We investigated the ultrastructure and protein composition of the cytoskeleton-like material of the AO with several forms of microscopy and biochemical analysis, to determine whether the AO was constructed at the molecular level on principles similar to those of other mycoplasmas, such as and We found that the AO interior was generally dissimilar from that of other mycoplasmas, in that it exhibited considerable heterogeneity in size and shape, suggesting a gel-like nature. In contrast, several of the 12 potential protein components identified by mass spectrometry of detergent-insoluble proteins shared certain distinctive biochemical characteristics with AO proteins, although not with proteins. We conclude that convergence between and AOs extends to the molecular level, leading to the possibility that the less organized material in both and is the substance principally responsible for the organization and function of the AO. is a bacterium that infects HIV-positive patients and may contribute to the progression of AIDS. It attaches to host cells through a structure called an AO, but it is not clear how it builds this structure. Our research is significant not only because it identifies the novel protein components that make up the material within the AO that give it its structure but also because we find that the AO is organized unlike AOs from other mycoplasmas, suggesting that similar structures have evolved multiple times. From this work, we derive some basic principles by which mycoplasmas, and potentially all organisms, build structures at the subcellular level.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5446615 | PMC |
http://dx.doi.org/10.1128/JB.00069-17 | DOI Listing |
Biomolecules
November 2024
Department of Biology, Washington University, St. Louis, MO 63146, USA.
Mitochondrial holocytochrome c synthase (HCCS) is an essential protein in assembling cytochrome c (cyt c) of the electron transport system. HCCS binds heme and covalently attaches the two vinyls of heme to two cysteine thiols of the cyt c CXXCH motif. Human HCCS recognizes both cyt c and cytochrome c of complex III (cytochrome bc).
View Article and Find Full Text PDFMethods Mol Biol
December 2024
Mechanobiology Institute, National University of Singapore, Singapore, Singapore.
YAP is a central regulator of the Hippo-YAP signaling axis, an evolutionarily conserved pathway that modulates organ growth and regeneration. Dysregulation of YAP signaling leads to uncontrolled proliferation, promoting epithelial-to-mesenchymal transition and invasion in cancer metastasis. Exogenous manipulation of YAP activity at the second-to-minute timescale is an important step in studying the signaling pathway.
View Article and Find Full Text PDFMedicine (Baltimore)
December 2024
Department of Neurology, The Affiliated Hospital of Southwest Medical University, Luzhou, China.
Methods Mol Biol
December 2024
Molecular, Cellular, Developmental Biology and Genetics Program, University of Minnesota, Minneapolis, MN, USA.
Throughout the cell, motor proteins work together to drive numerous molecular processes and functions. For example, ensembles of myosin motors collectively transport vesicles and organelles, maintain membrane homeostasis, and drive muscle contraction. Studying these motors in groups has become increasingly important with work demonstrating the emergence of ensemble behavior distinct from individual motor behavior.
View Article and Find Full Text PDFInt J Mol Sci
November 2024
Department of Biomedical Sciences, Chubu University, Matsumoto 1200, Kasugai 487-8501, Aichi, Japan.
Extracellular vesicles (EVs) play important roles in intercellular communication in various biological events. In particular, EVs released from cancer cells have attracted special attention. Although it has been reported that cancer-associated glycosphingolipids play important roles in the enhancement of malignant properties of cancer cells, the presence, behavior, and roles of glycosphingolipids in EVs have not been elucidated.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!