topic 2 - cells Flashcards

(94 cards)

1
Q

strutcutres within the neuculeus

A

neuclear envelope - double envelope
neuclear pores
neucleoplasm - granualr jelly like mateiral
chromozones - protein bound linear dna
neuclouous - small sphere inside this is the site of rna production and makes ribsomes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

fnuctin of neucles

A

site of dna replicatoin and transcription ( makinng of rna )
contains the genetic code for each cell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

edoplasmic reticulum - strutcure

A

rough and smooth er both have folded membrenes called cisternae
rough have chromozones on the cisternae

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

function of endoplasmic reticulum

A

RER - protien synthesys
SER - synthesys and store lipids and carbs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

golgi appararus - structure

A

folded membrene make cisternae
secretart cesticles pinch of from the cisternae

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

golgi apparatus and vesicles - function

A

add cars to protiens to form glycoprotiens
produce secretory enzymes
secrete carbohydrates
transport, modify and store lipids
form lysozomes
molecules are labeld with their destination

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

lysozomes structure

A

bags of digestive emzymes - can contain up to 50 enzymes.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

lyspzpmes function

A

hydrolise phagocytotic cells
completely break down dead body cells
exocytosis - release enzymes to outside of the cell to destriy materal
digest worn out organels for reuse of amterials

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

mitochondria structure

A

double membrene
inner membrene called cristae
fluid ctnre called mitochondrial matrix
loop of mitochondrial dna

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

mitochondria function

A

site of aerobic resporatoin
site of atp production
dna to code for enzumes needed in respiration

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

ribozomes streutcure

A

small made up of two sub units of protien and rna

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

robozomes fucntoin

A

site of priten synethsys

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

vacuole structure

A

filled with fluid surrounded by a single membrene - tonoplast

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

vacuole function

A

make cells tugrid and therefore provide support
temprary store of suagrs and amino acid
pigmant may colour petals attratcing polinators

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

cholroplats structure

A

surrounded by a double membrene
contrain thylakiods ( folded membrenes embreded with pigment )
fluid filled stroma contains enzyme for photosynthesys found in plants

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

key difference between prokaryotic and eukaryotic cells

A

the cells are miuch smaller ]
no membrene bound organelles
smaller ribosomes
no neuculeus
cell walled made of muerin

they may also contain
plasmids, flagela, a capsule around the cell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

define magnification

A

how many times larger the image is comared to the object

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

define resolution

A

the minimum distance between two objects in wich they can still be views as seperate
the resolution of a light microscope is determined by the wavlenength of light and the wavelenegth of the beam of electrong derermines the resolution in electron microscope

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

optical microscooe - key points

A

a beam of light is condensed to creat an image
poorer resolutioun is due to light having a longer wavelength
lower magnification
colour images
can view living samples

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

electron microscope ( key points )

A

scanning or transmission
a beam pf elecvtrons is considred to creat the image, electromagnets are used to condense the beam
higher resolving power as electrons have a short wavelength
hgiher magnification
black and white images
sample must be in a vacume therefore non living

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

how do transmission electron microscopes work?

A
  • thin specifmine is stained and placed in a vacume
    electron gun produces a beam of electrons that pass through the specimen
    some parts absorb the electrons and appear dark
    image is 2d and shoes the internla structure of cells
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

how do scanning electron microscpoes work?

A

do not need to be thin.
electronsd are beamed onto the surfsce and scattred in different ways depending on the contours
prodcing a 3d image

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

image size= ?

A

actual size x magnification
i = am

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

how to convert!!

A

metre
millimitre
micrometre
nanometre

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
cell fractionation solution - 3 conditions and why?
cold - reduce enzume activity, when the cell brekas open enzymes are realeased wich could damage the organelles isotonic - same water potential to prevent osmosis causing the cells to shrivel or burst buffred - the sulution has a pH buffeer to prevent damage to organelles
26
two steps to the process of fractionation
homogenisation ultracentrifugation
27
outline step one of cell fractionation
homogenisation cell must be broken open using a blender cells are blended in a cold isotonic buffered solution solution is fulred to remove large cell debri
28
outline the steps of differential ceitrifugation
centrifuge spins and the centrifugal forces scause pellets of the most dense organels to fomr at the bottom centrufuge is first spunat low speends and this process is repeated at increasingly faster speeds each time the supernatant is removed leacing behing a pelet of organells
29
heaviest - lightest - differential centrifugation
nucleui chloroplats mitochondria lysozomes endoplasmic reticulum ribosomes
30
what arr the three phases of the cell cycle?
interphase neuclear division cytokenesis - division of the cytoplmasn to creat new cells
31
mitosis four key stages
prophase metaphase anaphase telophase
32
reuslts of mitosis
one round of division genetically ideittcal cells are made diploid cells are made growth and repair e.g clonail expansion of b cells
33
outline prophase
chromozones condense and become visible
34
outline metaphase
chromonseones align along the equator of the cell, spindle fubred released from the poles now attatch to the centromere and chromtid
35
outline anaphase
the spindle fibred start to retraxct and pull the centromere and chromotids rhey are bounf towats the oposite ples centromere divided in teo snd indivial chromatids and pulled to each oposite pole this stage rewuiured energy in the form of atp
36
outline telophase
chromonses are now at each pole and become konger and thinner again the spindle fubres desintegrate and the neucleus starts to reform
37
mitotic index is?
( the number of cells in mitossi / the total number of cells ) x 100
38
binary fission in prokaryotic cells
repliaton of circular dna and plasmids division of the cytoplasm to produce two daughter cells each with a snigle copy of the circular dna and a variable number of plasmids
39
why do viruses not under go cell division?
they are non living they inject their neucleic acid into the host and the host cell replicates the virus particles
40
what is the cell membrene called?
phospholipid bylayer
41
hydro...
hydropohpbic tail hydrophilic head
42
what is colestrols purpose in the membrene
restirct larteral movement of other molecules in the membrene. this is useful as it makes the me,brene less flid at hight empretruews and prevents water and disolved ions leaking out of the cell
43
different types of protiens in the membrene
peripheral protiens provide medhanical support so they are conected to protiens or lipids to make glychoproptiens and glycholipids. the function of these is cell recognition as receptors intergrap protiens are protien carriers or chal proriens involved in the transport of molecule across the membrene protien chalens form rubes filled with water to enable water soluble ions to diffuse carrier protiens will bind to other alrger moelcules such as glucose or amino acids and change shape to transport them to the other saide of the membrene
44
molecules that passs through the plasam membrene
lipid soluble subsutances and very small molecules
44
molecules that can not pass through the membrene
water soluble subcustances and alrge molecules ( sodium ions ) ( glucos )
45
simple difusion
the net movement of moleucles from an area of higher conetrantaion to an area of lower contentratoin until equilibrrium is reached., this process does not require atp
46
facilitated diffusion
passive process but different from simple diffusion as pprotiens are used to transport molecules the movement of ions and polar molecules wich can not simply difuse can be transport across by fd using protien chanels and carirer protiens
47
how to protien channels work?
fomr tubes filled with water and enabled wayter solubule ions to pass through the membrene this is still electivre and the chanel is only open in the presence of certsin ions
48
how do carrier pritens work?
will bind with a molecule e.g glucos this will change the sdhape of the priotien the shape change enables the molecule to be released to the other side of the membrene
49
what is osmosis
movement of water from an are of higher water potentials to an area of lower water potental acorss a partially permebable membnrene
50
what is water pottential
the pressure created by water molecules and is measured in kpa pure water has a warer potental of 0
51
what is an isotonic solution?
the water potential is the same in the solution and the cell within the solution
52
what is a hypotonic solutoin?
the water potential of a solution is more positive ( closwe to zero ) than the cell
53
hypertonic solution?
the water potential pf the solution of mroe negative than the cell
54
what is active trnapsort?
the movement of subcustnve from a low contentration to a high conetration using metaboilic energy and a carrier protien
55
steps to a active tranpsort using a carrier protien?
1. transport is thorugh carirer protiens spanning the cell membrene 2. molecule binds to a receptor complementory in shape to the protien 3. atp binds to the carrirer prietien from the indise of the cvell and is hydrolised into adp and +pi 4. this causes the carrier pritoen to change shape and release hte molecule onto the other side 5. the phosphate ion is then released and the protien returns to its original shape
56
co transport of glucose and sodium ions ion the ileum
to absorb glucose from the lumen to the gut there must be a higher concentratoin of glucose in the lumen compared to the epithelial cell ( for facilitaed diffusion ) but there is usually more glucos in the epithelial cells thjis is why active tranpsort and co trnapsort are reuqired
57
co tranpsort of glucose and sodium ions in the ileum
sodium ions are activelty transported out of the epitheilial cells into the blood thhis reduced the sodium ion concentratoin in the epithelial cell sodium ions can then difuse from the lumen down their cocentration gradient into the epithelial cell the protien the sodium ions difucse thorugh is a co trnapsorter protien so either gluce or amino acids can also attatch and are transported into the epithelial cell against their concentraoitn gradient
58
cells may be adapted for rapid trnapsort scross their internal or external membrenes by:
an increase in surface area an increase in the number of pritein chanels and carrier molecules in their membrenes
59
how can lymphocytes distinguish betwen pathogens and self cells?
each type of cell has specific molecules on its surface that identify it. these molecules are usually protiens as their 3d teritary structuire enables lots of unique and identifiyable shapes to be made
60
if a non self cell is detected a repsonse will be triggered to destroy the cell these different surface molecules enable them to identify?
- pathogens - cells from other roganisdms of the same species - abnormal body cells - toxins
61
what are antigens?
molecules that generate an imune repsonse bt lymphocyte cells when detected in the body they are uaually protiens and are locsted on the surface of cells
62
what is antigen varibaility?
pathogenic dna can mutate frequently if a mutatoin occues in the gene wich codes for the antigen the dshape of the antigen will change. any previous immunity to this pathogen ( wither naturally occusing or atriifcially ) if no longer effective this is becuase the memory cells will have a memory of the old antigen shape e.g the influenza virus changes its antigens very quickly, therefore we need a new flu vacine each year
63
what is the difference between phagocytes and lymphocytes?
phagocytes - non specific lymphocytes - specific
64
steps to phagocytosis
phagocytes are in the blood and tissues any chemicals or debris resleasded by the pathogen or abnormal cells will attrasct the phagocytes and they will move toward the cells there are many receptor binding points on the surface of the phagocytes they will attatch to chemicals or antigens on the pathogen via these recptors the phagocyte changes shape to move around the pahtogen and engulf it once engulphed the pathogen is contained with a phagozome vesicle a lysozome within the phagocyte will fuse with the phagozome to reslease its contents the lysozome enzyme is relased into the phagozome this is a lytic enzymw wich hydrolises the pathogen
65
what do cell mediated responses involve?
t cells and body cells
66
where to t cells marture?
thymus.
67
what are antigen presenting cells?
any cell that presents a non self antigen on its surface.
68
what are types of antigen presenritng cells?
infected body cells will presenrt viral antigens on its surface a macrophage wich has engulphed and sdestroyed a pathofen will presernt the antgens on their surface cells of a transplanted organ wull have different shaped antigens on their surface conmapred to your self cell antigens cancer sells will have abnornal shaped self cell antigens
69
steps to the cell mediated reposnse
1. once a pathogen has been engulphed and destroyed by a phagocyte the antigens are positiojned on the cell surface 2. this is now called an antigen presenting cell 3. helpcer t cells have receptors on their surface wich can attatch to the antigens on the apc 4. once attatched this activates the helper t cells to divide by mitosis to replicarte and make a alrge number of clones 4. cloned helper t cells differentiare into different cells - some reaim has helpter t cells and activate b lymphocytes - some stimulate macrophages to perform mroe phagocytosis - some becuase memory cells for that shaped antgen - some became cytotoxic t cells ( killer t cells )
70
what are cytotoxic t cells?
these cells destroy abnormal or infected cells they release a protein, perforin wich embeds in the cell surface membrene that makes a pore ( a hole ) so any subcustance can enter or leave a cell
71
what do cytotoxic t cells cause?
cell death this is more common in viral infections becuase viruses infect body cells body cells are sarificed to prevent viral replicatoin this is why you gert a sore throat
72
what are lymphocytes
white vlood cells involved in the specific imune response
73
where are lympocites made and matured
bone marrow b cells mature here to
74
steps to b cell activation.
antigens in the blood colide with their complementty antibody on a b cell the b cell takes in the antigen by endocytosis and then presents it on its cell surface membrene when this b cell colides with a helper t cell receptor this activates the b cell to go thorugh clonial expansion and differentiation b cells undergo mitosis to make large numners of cells these differentiate into plasma cells or memory b cells plasma cells make anti bodies b cells can divide rapidyl into plasma cells when re infected with the same pathogen to make large numbers of antibodies rapidly
75
memory b cells live for...
decades
76
memory b cells do not make antubodies rather they?
divide by mitosis and make plasma cells rapidley if they clode with an sntigen they have previously enountred this results in large numbers of antibodies being produced rapidly that the pathogen is destroyed before any symptoms can occur
77
what is agglutinaton ?
antibodies are flexible and can bind to multiple antigens and clump them together this makes it easier for phagocytes to locate and destroy the pathogens
78
what is passive imunity?
antibodies are introduced into the body the pathogen doesnt enter the body so plasma cells and memory cells are not made no long term immunity e.g naitbodies passed to a fetus thorugh placenta or through breast milk to a baby
79
what is active immunity?
imunity created by your own imune system following exposure to the pathogen or its antigen
80
what is antural active immunity?
following infextion and the creation of the bodys own anti bodiies or memory cells
81
what is artifical active immunity
following the introduction of a weakned version of the pathiden or antigens via a vaccine
82
how do vaccines work?
small amounts of weakned or dead pathofens are introduced into the mouth or by injection exposure to the antigens activasted the b cell to go thorugh clonail expansion and differentatoin b cells undergo mitosis to make large numbers of cells rhese differenriate into plasma cells or memory b cells plasma cells make antibodies b memory cells can divide rapidly into plasma cells when reinfected witht he same pathogen to make large numbers of antibodies rapidly
83
what is herd immunity
if enough of the population are vaccinated the pathfgeon can no spead easiuly among the popualtion this privides protection for those who are not able to get vaccinated
84
hiv strutcture ( 4 components )
core - genetic material ( rna ) and the enzyme reverse transcriptase wich is needed fo viral infectoin capsid - outer protien coat envelope envolope - extras outer layer protien attatchments - on the evterior of the envoleope to allow the virus to attatch to the hosts helper t cell
85
repliatoin of hiv in helper t cells
hiv is transported around the blood until it attstched to a. cd4 protien on the helper t cells the hiv protiem capsule then fuses wirth the helper t cell membrene enableing the rna and enzymes from the hiv to enter the hiv enzyme reverse transcriptase coppised the viral rna into a dna copy and moves to the helper t cell neuculsi, this is why it is called a retrovirus here mrna is transcribed and the helper t cell starts to creat ivral protiens to make new viral particles
86
aids is when the ...
replicsting viruses in the helper t cells interfere with their normal fucntoining of the imune system with the helper t cells being destroyed by the virus the host is a ubable to produce an adequite response to other pathogens and is left vulnerable to infectoins and calcer it is the distruction of the imune system that lead to death rather than the hiv directly
87
what are monoclonal antibodies
a single type of anti body that can be iscolated and cloned
88
moncolonal anti bodies have been created for:
medical treamtnet diagnosis pregnancy tests
89
what is indirect moncolonal antibody therapy
drugs attatched to them delivreded directly to cnacer cells and kill them reeucded the harmful side effects of chemotherapy often refered to as bullet drugs
90
monoclonal antibodies can be used to test for:
pregnancy influenza hepatitis chlamydia prostate cancer this works via the eliza test
91
eliza test - use of two antibodies!
first mobile antibodu competelemtry to the antibody being trsted foand had colourred a second antibody compeltementry in shape to the antigen is imoblised in test a third antobody is imoblised and is completemrry to the shape of the first antbody
92
steps of the eliza test
add the test sample from as patent to the base of the beaker wash to remove any unbond test sample add an antibody compeltemtry in shape to the antigen you are testing the presence of in the test sample washto remove any unbound antibody add a second antibdoy that is compeltentry to the shape of the first antibody and binds to the first the second antibody has an enzyme attratced to it. rinse the unbound antibodies off the substrate for the enzyme wich is colourless is added the substrate produces coloured products in the presence of the enzyme the presnce of the colour indicated the presence of the antigewn in the test sample and the intensity of the colour indicates the quanitity present
93