This article contains short answer questions on Biomedicine Cell Module covering topics like amino acid structure, protein chain, quaternary structure, mitochondria, chloroplast, cell differentiation, extracellular matrix, neoplasms, haemocytometer grid, cell culture and temperature effects.
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Answer the questions appropriately. Your answer should be in red or highlight the appropriate answer in red. Section A Answer ALL short questions in the spaces provided. 1.Identify the alpha carbonmolecule in the amino acid structure below. Ans: carbon no. 2 (Total 2 Marks) 2.The primary sequence of a peptide is shown below: ALIPFQVWGC (a)Which amino acid is present at the carboxyl terminus of the peptide?Ans: Cystenine amino acid (2Marks) (b)Complete the sentence: The amino acids in this peptide sequence predominantly have ___Nonpolar____________ side-chains. (i)Basic
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(ii)Acidic (iii)Uncharged polar (iv)Non polar (1 Mark) (Total 3 Marks) 3.In a protein chain, around which of the following isnorotation observed? (a)C‒N peptide bondAns:C-N peptide bond (b)N(H)‒Cabond:f(phi) (c)Ca‒C(=O) bond:j(psi) (Total2 Marks) 4.For which of the following proteins is correct quaternary structure important for function? (select as many options as are relevant) (a)Coronavirus spike protein Ans:Coronavirus Spike protein (b)HaemoglobinHaemoglobin (c)Trypsin (d)Immunglobulin G (Total2 Marks) 5.Which organism does the mitochondria and chloroplast evolve from? Ans: Prokaryotes (Total 1 Mark) 6.Name the process of cell drinking. Ans: Pinocytosis (Total 1 Mark)
7.Briefly describe how non secretory proteins are targeted to their correct locations and list 3 destinations for proteins following the non- secretory pathway. (Total 4 Marks) Ans: Non- secretory pathway mainly includes targeting of proteins as follows: Cytoplasm, Mitochondria, Peroxisomes, and nucleus. There are four location inside the mitochondria to which protein is transported. They are mitochondrial matrix, inter membrane space, inner membrane and outer membrane. Mechanism of proteins targeting into matrix: precursor protein prepare on cytosolic ribosome recognised by MTS receptor then transported to import channel then after destined for the mitochondrial matrix at contact sites where N- terminal of proteins enter into the mitochondrial matrix. Final folding of protein are completed in the matrix. Targeting to inner membrane of mitochondria involves three pathway and for intermembrane space involve 2 pathway. 8.Where is ATP synthase located within the mitochondria and chloroplast? ANS: In eukaryote, the ATP synthase is located in the inner membrane of mitochondria and in the plant ATP synthase enzyme located additionally in the thylakoid membrane of chloroplast. (Total 2 Marks) 9. (a)Describe the term “cell differentiation”. ANS: cell differentiation is the process through which young, immature cells change there function and phenotypical type. (1 Mark) (b)Draw a blastocyst and label the key parts and their fates. (3 Marks) Ans:
Inner cell mass differentiates into an embryo.Blastocoel change into embryonic gut cavity and trophoblast converted into epithelial cells (Total 4 Marks) 10.Describe the difference between a totipotent and unipotent cell. Ans: totipotent cells are capable to differentiating into all types of body cells whereas unipotent cells are differentiate into only limited fixed cells. (Total 2 Marks) 11.Name a protein found in the extracellular matrix and describe its function. Ans: collagen protein is majorly found in extracellular matrix. It provide tensile strength, support chemotaxis and migration and direct tissue development and regulate cell adhesion. (Total 2 Marks) 12.List two of the major types of connective tissue found in the human body. Ans: Blood and bones (Total 2 Marks)
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13.Describe the process involved in the activation of a receptor tyrosine kinase (RTK) following ligand binding. Ans:cross-linking activates the tyrosine kinase activity in these RTK through phosphorylation specially, each RTK in the dimer phosphorylates multiple tyrosine on the other RTK. This process is called as cross- phosphorylation. The tyrosine kinase phosphorylates a G protein, activating this. At the time of ligand binding, RTK that bind to peptide hormone may form dimer. Ligand binding activates the receptor's kinase activity and cause auto phosphorylation of tyrosine residue in the cytosolic domain. (Total 5 Marks) 14.What is the collective term used to describe malignant tumours which are derived from connective tissues? Ans: Sarcomas (Total 1 Mark) 15.Both intrinsic and extrinsic apoptotic pathways converge on a single caspase. State which caspase this is. Ans: Capsae 3 (Total 1 Mark) 16.Provide a definition of the following: (a)Endocrine signalling :A cell targets a distant cell through the bloodstream. (b)Paracrine signalling :A type of cellular communication in which a cell produces a signal to induce changes in nearby cells. (c)Juxtracrine signalling :It is a type of cell-cell or cell- extracellular matrix signalling in multicellular. (Total 3 Marks) 17.
(a)D i f f e r e n t i a t e between characteristics of benign and malignant neoplasms. Ans:Benign: invade near by tissue and can not spread to other parts of the body. Malignant: travel through blood or lymphatic system to other parts of the body and able to invade nearby tissue. (3Marks) (b)Mention the 3 factors linked to the virulence ofHelicobacter pylori. Ans: Disease induction, immune escape, and colonization (4Marks) (Total 7 Marks) 18. (a)What type of microorganism is contaminating the culture in the picture shown below? Note: Image B below shows a high-power view of the square highlighted in A below. Ans: Bacterial infection cell culture. (1Mark)
(b)What is the nature of the contamination shown below? Ans: Destructive nature (1Mark) (c)Please identify the following micro-organisms regarding colony formation and gram classification. ANS: Staphylococcus aureus, gram positive bacteria (1 Mark)
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(d)If a culture goes from 22% confluency to 88% in a 24-hour period, what is the doubling time? Show your calculations below. Ans: 12 hours (2 Marks) (Total 5 Marks)
19.Below you will find a haemocytometer grid that has been loaded with cell suspension mixed with trypan blue. You need to calculate cell viability, cell concentrations and seeding density for this particular cell suspension (show your workings). For each corner square, record the cell counts in the following table: CORNER SQUARE VIABLE CELLSDEAD CELLSTOTAL CELLS A14620 B14519 C11617 D18523 MEAN (N)14.255.519.75 (a)One hundred microlitres of cell suspension was mixed with four hundred microlitres of trypan blue. Calculate the dilution factor (D) due to adding trypan blue to the cell suspension. Ans: Dilution factor = (100+400)/ 100 = 500/100 = 5 (2Marks)
(b)Calculate the percentage viability. Ans: (total number of live cells / total number of cells)* 100= (57/79)*100= 84.4% (2Marks) (c)Now calculate the number of cells per mlof cell suspension, using the following equation and present this in standard form. Cells/ml of suspension = N x 104 x D =19.75* 10^4* 5 = 987500 (2 Marks) (d)You need to plate out your cells at a seeding density of 1.5 x 105cells per well. First calculate what volume of your cell suspension you need to use to obtain this inoculum. Ans:since for 98.75*10^4 cells are found in 1ml, Therefore, for 1.5* 10^5 cells we required = (1ml/ 98.75*10^4)* 1.5*10^4= 0.14 ml suspension (1 Mark) (e)Then calculate the volume of medium required per well to give a total volume of cell suspension plus medium of 2ml. Ans: 0.14/5=0.018 ml and for 2 ml 0.4ml volume of medium required.(1 Mark) (Total 8 Marks) 20.What are the possible effects of these temperatures on cell culture? 4°C, 42°C, 37°C
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(Total 3 Marks) Ans= at 4degree temperatures= cell growth inhibit at 37 degree temperature = normal cell growth. At 42 degree temperature = protein coagulate so inhibit cell growth