Pintar - Cell Structure II Flashcards
integral membrane protein
peripheral membrane protein
integral - transverse the entire width of the cell membrane. Have 3 domains - cytoplasmic, membrane-spanning, external
peripheral - attached to the cytoplasmic/extracellular side by non-covalent interactions.
why is it that when you split a membrane there on more proteins found on the cytoplasmic side of the membrane?
The proteins are stabilized by the cytoskeleton on the inside of the cell. In the RBC, the cytoskeletal proteins are called actin and spectrin.
Hereditary spherocytosis
In the absence of spectrin the RBCs will become more spherical and be more likely to become phagocytized. This is because spectrin is involved in the upkeep of the structure/stability of the cell. It becomes more sensitive to osmolarity.
Functions of membrane proteins
1) can be linker/anchor molecules that such as those that interact with cytoskeletal proteins (spectrin)
2) transporter molecules
3) receptors
4) enzymes
Brush Border
Plasma Membranes can have modifications to them. One such example is the brush border in which there are microvilli on the end of the apical surfaces of enterocytes. This increases the surface area for absorption. On t he edge of the microvilli is glycocalyx. On the lateral borders of these cells are junctional complexes that allows for the cells to adhere to each other.
glycocalyx
oligosaccharide side chains attached to things on the PM. So, we have proteoglycans, glycolipids, and glycoproteins.
microvilli
As was mentioned earlier, microvilli are on the surface of many cells PM. Microvilli are made up of bundles of actin filaments. These filaments are surrounded by the PM and have a glycocalyx coat on their tips. The bottom of the actin filaments congregate in what is called the Terminal Web. Myosin is also involved, which acts as a motor to move things up and down the actin. Actin is also involved in the cytoskeleton.
Different junctional complexes
tight/occluding junctions (zonuda occludens)
belt desmosomes (zonuda adherens)
spot desmosomes (macula adherens)
communicating (gap junctions)
microtubules
Are made up of a protein called tubulin. Is found in cilia, centrioles, and mitotic spindles.
smooth ER
Site of lipid synthesis, Ca2+ storage, detoxification, metabolism of drugs and steroid synthesis. In a cell that is heavily involved in making steroids, you will see a lot of SER. There are no ribosomes. Site of many heme-linked proteins.
Rough ER
Ribosome studded. Is essentially connected to the nucleus. Is able to translate all of the mRNA that is excreted from the cell. Once the proteins have been synthesized, they will go to the golgi where they are sorted and packaged. Cells with a lot of RER are indicative of having proteins entering the secretory pathway. The rRNA will bind positively charged dyes and create “basophilia.”
Golgi apparatus
flattened membranes where proteins enter at the cis face and leave from the trans face. Cis face is right near the RER whereas the trans fce is near the PM. There is a medial face in between. Once vesicles are ready to leave, they depart from the trans face in a place called the “trans golgi network (TGN).”
constitutive vs. regulated secretion
C - there is little if any secretory granules sitting around because they are always being secreted. This would be like in plasma cells where they constantly secrete antibodies.
R - large numbers of vesicles/granules accumulate in some secretory cells. An external stimulus will then tell the cell when to excrete it’s contents.
endocytosis
a ligand binds to an external receptor thus causing the membrane to pinch in and form a vesicle. The invagination is initiated by coat proteins, one type is called clathrins. The vesicle and coat proteins form what is called a coated pit in order to detach from the PM. It is then called a coated vesicle. The coated vesicle can then form with an early endosome. Endosomes are where things that just entered the cell are sorted.
Differences in mito depending on cell?
of cristae changes depending on the energy needs of the cell. The more cristae the more energy. Shape of mito can change as well (morphology).