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Kedise mmọ mkpụrụngwa ọzọ a ma apụtara n'osisi yi?
Kedise mmọ mkpụrụngwa ọzọ a ma apụtara n'osisi yi?
Kedu ihe bụ ọrụ nke AP1 na usoro a?
Kedu ihe bụ ọrụ nke AP1 na usoro a?
Kedu ụzọ nke secreción na-apụta na cell niile?
Kedu ụzọ nke secreción na-apụta na cell niile?
Kedu ọrụ ndị receptor MP6 na membrana Golgi?
Kedu ọrụ ndị receptor MP6 na membrana Golgi?
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Kedu ebe hidrolasa na-aṅụrịrị ogologo ọrụ?
Kedu ebe hidrolasa na-aṅụrịrị ogologo ọrụ?
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Ké emi inya uriọk uyo n'ibene enye?
Ké emi inya uriọk uyo n'ibene enye?
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Ké ukara ke inyen enye n'ibed ndokpo?
Ké ukara ke inyen enye n'ibed ndokpo?
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Ké mkpọ ikong ke proteínas Rab?
Ké mkpọ ikong ke proteínas Rab?
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Ké ini nyin ke proteins SNARE?
Ké ini nyin ke proteins SNARE?
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Ké ini ami proteins Rab?
Ké ini ami proteins Rab?
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Ké ini na adia esing ke proteins Rab n'ibed?
Ké ini na adia esing ke proteins Rab n'ibed?
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Ukpọrọb lipídic membrane kè smit proteins SNARE?
Ukpọrọb lipídic membrane kè smit proteins SNARE?
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Ké mkpọ ikong proteins GEF?
Ké mkpọ ikong proteins GEF?
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Kediek nyin esie odudu ubong mbakara ikang yene?
Kediek nyin esie odudu ubong mbakara ikang yene?
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Ibom enye onyo edim-re enyi?
Ibom enye onyo edim-re enyi?
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Kediek mmo ye ajọ ikang protein na Golgi?
Kediek mmo ye ajọ ikang protein na Golgi?
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Kediek ibom mmo re protein esiere ezali na vesículas?
Kediek ibom mmo re protein esiere ezali na vesículas?
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Nyin kiet esit ikang protein na ribosomas?
Nyin kiet esit ikang protein na ribosomas?
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Kediek ibom kiet protein mikọrọ mmo?
Kediek ibom kiet protein mikọrọ mmo?
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Kediek ikang protein esie ubong ikang umọn?
Kediek ikang protein esie ubong ikang umọn?
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Kediek sīre yömechanism makpọ nset mmo?
Kediek sīre yömechanism makpọ nset mmo?
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Kpọmkọm, gịnị mere transportadores lisosoma ji eme ihe?
Kpọmkọm, gịnị mere transportadores lisosoma ji eme ihe?
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Nke a bụ eziokwu banyere ATPasa nke H+ na lisosoma?
Nke a bụ eziokwu banyere ATPasa nke H+ na lisosoma?
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Gịnị bụ isi nke isi mmalite dị iche iche nke lisosoma?
Gịnị bụ isi nke isi mmalite dị iche iche nke lisosoma?
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Nke a adịghị enye ngosipụta nke lisosoma?
Nke a adịghị enye ngosipụta nke lisosoma?
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Kedu usoro nke efu na-eme ka edebe efu?
Kedu usoro nke efu na-eme ka edebe efu?
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Kedu ihe dị na bodies residual?
Kedu ihe dị na bodies residual?
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Nke a bụ eziokwu banyere macrophages na neutrophils?
Nke a bụ eziokwu banyere macrophages na neutrophils?
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Kedu ihe bụ jiri akụkụ ahụ na-arụ ọrụ nke lisosoma?
Kedu ihe bụ jiri akụkụ ahụ na-arụ ọrụ nke lisosoma?
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Ké akpọrọ usoro nke ngwanrọ peroxisoma?
Ké akpọrọ usoro nke ngwanrọ peroxisoma?
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Ké nwa ngwanrọ nwere olileanya nwere DNA na ribosomes?
Ké nwa ngwanrọ nwere olileanya nwere DNA na ribosomes?
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Ké enzyme nke anọchiteme n'ime peroxisoma?
Ké enzyme nke anọchiteme n'ime peroxisoma?
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Ké ụdị protein na akpọrọ peroxins?
Ké ụdị protein na akpọrọ peroxins?
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Ké ebe ndị peroxisomas dị elu n'ahụ mmadụ?
Ké ebe ndị peroxisomas dị elu n'ahụ mmadụ?
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Ké ụzọ na-abanye protein n'ime peroxisoma?
Ké ụzọ na-abanye protein n'ime peroxisoma?
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Ké ọtụtụ genes nke coding protein peroxisoma anọpụtara na genom humano?
Ké ọtụtụ genes nke coding protein peroxisoma anọpụtara na genom humano?
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Ké ụzọ peroxisomas na-ekekọta protein?
Ké ụzọ peroxisomas na-ekekọta protein?
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Kéde ndien esie keme isong isong ke membrana mitocondrial?
Kéde ndien esie keme isong isong ke membrana mitocondrial?
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Kéde ikó isong ke mmen ena yene mitocondrial?
Kéde ikó isong ke mmen ena yene mitocondrial?
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Kéde asana efen isong ke citosol?
Kéde asana efen isong ke citosol?
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Kéde ndien esie asana asana efen mmen ena yene ribosomas?
Kéde ndien esie asana asana efen mmen ena yene ribosomas?
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Kéde ndien isong ke porinas?
Kéde ndien isong ke porinas?
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Kéde ikó asana etok isong ke mmen mitocondrial?
Kéde ikó asana etok isong ke mmen mitocondrial?
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Kéde asana iké mmen allmɛn ke mitochondria?
Kéde asana iké mmen allmɛn ke mitochondria?
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Kéde asana asana iké citosol ke autophagosomos?
Kéde asana asana iké citosol ke autophagosomos?
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Study Notes
2º Partial Cellular Biology
- This is a study document for a second partial exam on cellular biology.
- The document was created by Paula Ferrández López.
- The course is 1st year of Medicine at the UCAM University with Sonia Sánchez as Professor.
Topic 11: Endoplasmic Reticulum
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The Endoplasmic Reticulum (ER) is a crucial crossroads for protein traffic in eukaryotic cells.
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The ER is involved in protein processing and distribution.
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Proteins synthesized by ribosomes bound to the ER membrane are generally destined for secretion, the ER, Golgi, lysosomes, or the plasma membrane.
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Proteins destined for the cytosol, nucleus, mitochondria, chloroplasts, or peroxisomes are synthesized by free ribosomes and released into the cytosol.
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The ER is a continuous membrane network extending from the nuclear membrane throughout the cytoplasm, forming a network of tubules and sacs/cisternas. It's the largest organelle in most eukaryotic cells.
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There are two main types of ER: Rough ER (RER) and Smooth ER (SER).
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RER has ribosomes on its surface and plays a role in protein processing.
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SER lacks ribosomes and is involved in lipid metabolism.
Topic 2: RER
- RER membrane is thinner than the plasma membrane (70% proteins and 30% lipids).
- It has two sides: a side facing the cytosol (with ribosomes) and a lumenal/light side (without ribosomes).
- RER stores proteins made by ribosomes, preparing them for glycolysation and packaging before being sent to other organelles or outside the cell.
Topic 3: RER protein synthesis pathways
- Co-translational: Proteins are translocated into the ER while they are still being synthesized by ribosomes. This is the most common pathway in mammals.
- Post-translational: Proteins are translocated into the ER after their complete synthesis, this pathway can be used in yeast.
- Signal peptides: These peptides direct proteins to the ER membrane. They are typically hydrophobic amino acids followed by a few basic amino acids; located at the N-terminal.
Topic 4: Protein translocation into the ER lumen
- Signal Recognition Particle (SRP): Binds to the signal peptide and the ribosome.
- SRP receptor: on the ER membrane, binds to the SRP and slows down translation temporarily.
- Translocation channel/Translocon: Protein-conducting channel in the ER membrane that guides the growing polypeptide chain into the ER lumen.
- Signal peptidase: cleaves the signal peptide once it's inside the ER.
Topic 5: Synthesis pathway
- RER → Golgi → Secretory vesicles → outside the cell pathway.
- RER → Golgi → plasma membrane, lysosome, and other destinations. Other times proteins stop at the RER or Golgi for further action.
- Proteins destined for other destinations than RER, Golgi, lysosomes, or plasma membrane are made on freestanding ribosomes. These proteins remain in the cytosol once translation is completed.
- Integral membrane proteins use a signal-anchor sequence that directs them into the ER membrane. Multi-pass transmembrane proteins need multiple start and stop signals.
Topic 6: Protein synthesis in the RER:
- Ribosomes synthesize proteins destined for secretion (e.g., plasma membrane) attach to the ER. This procedure enables the production of soluble proteins and integral membrane proteins.
- These proteins enter the ER, either during or subsequent to translation.
- Signal peptides on newly synthesized proteins direct them to the ER.
- SRP recognizes and transports the ribosome-RNA complex towards the ER membrane.
Topic 7: Synthesis of transmembrane proteins
- Proteins destined for the ER, Golgi, lysosomes, or plasma membrane are initially directed to the ER.
- Proteins that will remain in the cytosol or go to the nucleus, mitochondria, or other organelles will be synthesized on free ribosomes.
- Proteins will enter the ER during translation
- Proteins with signal peptide get targeted into the ER
- Proteins that will enter the ER need a signal peptide
Topic 8: SER Characteristics
- The SER is devoid of ribosomes
- It plays role in lipid metabolism: synthesis of lipids used for membrane development and hormone synthesis
Topic 9: Golgi Structure/Composition
- The Golgi is composed of flattened, stacked, and membrane-enclosed sacs called cisternae.
- Multiple cisternae, grouped into stacks of 4-6 form a dictyosome.
- The Golgi has a distinct cis and trans face.
- The cis face receives material from the ER, and the trans face buds off vesicles for the next destination.
- A network of tubules and cisternae are associated with cis and trans faces, as well as medial compartments.
Topic 10: Golgi Functions
- The Golgi apparatus processes, modifies, and sorts proteins/lipids from the ER.
- Material arriving from RER proceeds gradually through the cisternae.
- The Golgi modifies proteins or lipids and decides what will happen to them: membrane of plasma, being secreted, or being sent to lysosomes.
- The Golgi modifies N-linked oligosaccharides synthesized in the ER.
Topic 11: Lysosomes: Introduction
- Lysosomes are membrane-bound organelles that contain hydrolytic enzymes. The enzymes can digest various biological polymers (proteins, nucleic acids, carbohydrates, and lipids).
- Lysosomes are important for cellular waste disposal.
- Lysosomes contain acid hydrolases.
Topic 12: Acid hydrolases
- Lysosomes contain around 50 different types of acid hydrolases.
- These enzymes need an acidic environment (around pH 5) for optimal activity, and these are protected from the neutral pH of the cytosol by the lysosomal membrane
- The pH in lysosomes is maintained by an ATP-driven hydrogen pump in the membrane that imports H+ into the lysosome.
- Damage to the lysosomal membrane would lead to release of its acid hydrolases which could digest the cell.
Topic 13: Endocytosis and Lysosome Formation
- Lysosome formation involves a combination of secretory and endocytic pathways.
- Material is ingested into endocytic vesicles, then combines with early endosomes, matures into late endosomes, and finally fuses with preexisting or developing lysosomes.
- The pH in lysosomes is maintained by active proton pumps in the membrane.
- Cellular components/materials delivered via endocytosis.
Topic 14: Mitochondria: Structure and Function
- Mitochondria are double membrane-bound organelles with a characteristic inner membrane arranged into cristae. The outer membrane is relatively smooth, whereas the inner membrane has folds called cristae, increasing its surface area.
- The outer and inner membranes enclose distinct compartments: an intermembrane space and the mitochondrial matrix.
- The matrix contains ribosomes, DNA, and enzymes crucial for cellular respiration.
- The major function of the mitochondrion is ATP production using cellular respiration (oxidative phosphorylation)
Topic 15: Mitochondria: Composition of the Membranes
- The outer membrane of mitochondria possesses a high proportion of porins.
- The inner membrane of mitochondria has a high protein content.
Topic 16: Nucleus: General Characteristics and Functions
- The nucleus is a double membrane-bound organelle that contains the cell's genetic material (DNA).
- It's the control center of the cell, regulating its activities.
- It houses the genome (the complete genetic information of an organism).
Topic 17: Nuclear Organization/Composition
- The nucleus contains chromatin, consisting of DNA and proteins (histones).
- In nondiving cells, chromatin exists as a dispersed/extended material known as euchromatin.
- During cell division, chromatin condenses significantly to form chromosomes.
Topic 18: Cell Cycle
- The cell cycle is the series of events that takes place in a cell leading to its division and duplication.
- Interphase includes G1, S, and G2 phases, where the cell grows, replicates its DNA, and prepares for division.
- Mitosis is the process where the duplicated genetic material is divided into two identical daughter cells.
- There are different checkpoints in the cell cycle to regulate progression and ensure accurate duplication.
Topic 19: Mitosis - Stages
- Mitosis has distinct stages (prophase, prometaphase, metaphase, anaphase, telophase, and cytokinesis).
Topic 20: Meiosis - Introduction/Stages
- Meiosis is a specialized type of cell division that produces haploid gametes (sperm and eggs) for sexual reproduction.
- Meiosis I is a reductional division, and meiosis II is an equational division.
- Meiosis involves crossing over during Prophase I
- Meiosis involves several steps (prophase, metaphase, anaphase, and telophase) in both meiotic divisions that lead to 4 haploid cells.
Topic 21: Peroxisomes - Introduction
- Peroxisomes are single membrane-bound organelles.
- They contain enzymes that use oxygen to oxidize various substrates.
- Cellular respiration leads to ATP formation and is regulated by various checkpoints. Peroxisomes are particularly important for certain lipid metabolism processes.
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Nke a bụ ihe nkuzi gbasara atụmatụ na ọrụ nke proteins na sel. Quiz a ga-enyere gị ka ịmara nyocha mkpọrọb na membrane, ọrụ receptor, na ụzọ nyefee proteins. Nwetaghachi ihe ọmụma gị gbasara usoro mmepụta na ngwanrọ nke proteins.