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Microtubule and tubulin metrics [1]. Microtubules are polymers of tubulin that form part of the cytoskeleton and provide structure and shape to eukaryotic cells. Microtubules can be as long as 50 micrometres, as wide as 23 to 27 nm [2] and have an inner diameter between 11 and 15 nm. [3]
Inside a cilium and a flagellum is a microtubule-based cytoskeleton called the axoneme. The axoneme of a primary cilium typically has a ring of nine outer microtubule doublets (called a 9+0 axoneme), and the axoneme of a motile cilium has two central microtubules in addition to the nine outer doublets (called a 9+2 axoneme).
Microtubule polymerization is nucleated at the microtubule organizing center. An aster is a cellular structure shaped like a star , consisting of a centrosome and its associated microtubules during the early stages of mitosis in an animal cell.
Micrograph showing condensed chromosomes in blue, kinetochores in pink, and microtubules in green during metaphase of mitosis. In cell biology, the spindle apparatus is the cytoskeletal structure of eukaryotic cells that forms during cell division to separate sister chromatids between daughter cells.
In cell biology, the centrosome (Latin centrum 'center' + Greek sōma 'body') (archaically cytocentre [1]) is an organelle that serves as the main microtubule organizing center (MTOC) of the animal cell, as well as a regulator of cell-cycle progression. The centrosome provides structure for the cell.
Animal cells (and some filamentous fungi are thought to rely upon the microtubule cytoskeleton and associated motor proteins. Although plants, algae and fungi transport depends on myosins , which move along the actin cytoskeleton, certain organelles can move along microtubules in plant cells.
3D rendering of centrioles showing the triplets. In cell biology a centriole is a cylindrical organelle composed mainly of a protein called tubulin. [1] Centrioles are found in most eukaryotic cells, but are not present in conifers (), flowering plants (angiosperms) and most fungi, and are only present in the male gametes of charophytes, bryophytes, seedless vascular plants, cycads, and Ginkgo.
The β-tubulin subunit is exposed on the plus end of the microtubule, while the α-tubulin subunit is exposed on the minus end. After the dimer is incorporated into the microtubule, the molecule of GTP bound to the β-tubulin subunit eventually hydrolyzes into GDP through inter-dimer contacts along the microtubule protofilament. [17]