2.1 Cell structure Flashcards
What is the equation for magnification
Magnification = image size/ actual size
What is cell fractionation and what are the 2 main steps
- The process where cells are broken up and their organelles are separated so they can be studied in detail.
- The 2 main steps are homogenisation and ultracentrifugation.
Describe the process of homogenisation
- The cells are broken up by a homogeniser to release organelles from the cell.
- This forms the resultant fluid called the homogenate. This contains the organelles, cell membrane and cells which were not broken up.
- The homogenate is then filtered to remove complete cells which were not broken, as well as large cell debris.
Describe the process of ultracentrifugation
- The filtered homogenate is spun in the ultracentrifuge to seperate out the fragments at a very high speed.
- This forms a sediment pellet at the bottom containing the heaviest organelles, e.g. nuclei, and a fluid called a supernatant.
- The supernatant is then transferred to another tube and spun faster to create a new pellet.
what are the conditions necessary for cell fractionation
A cold, buffered solution with the same water potential as the cells.
Why must the solution be cold
- Causes the enzymes present in the cell to work slower.
- This prevents them from breaking down organelles.
Why must the solution be buffered
- To keep a constant pH so that enzymes and other proteins in the cell don’t denature.
- pH interferes with bonds in proteins tertiary structure.
Why must the solution have the same water potential as the cells
- Same water potential (isotonic) means no osmosis will occur.
- This will prevent the organelles from shrivelling or bursting under osmotic pressure.
What is the order of fractination in cell fractination (order of organelles in pellets)
- Nucleus
- Chloroplasts
- Mitochondria
- Lysosomes
- Endoplasmic reticulum
- Ribosomes
What is contrast
The difference between the lightest and darkest parts of an image. It can be increases by staining.
What is magnification
The number of times an object has been enlarged.
What is resolution
The minimum distance apart that 2 objects can be in order for them to appear as separate items.
How do light/optical microscopes work
They work by passing light through a specimen and focusing the light on an eyepiece or camera which magnifies the image.
What are some advantages of light microscopes
- The specimen can be living.
- Simple preparation of specimen, so unlikely to distort cell structure.
What are some disadvantages of light microscopes
- Lower magnification (than electron)
- Visible light has a longer wavelength than electrons, creating a lower resolution.
How do Transmission Electron Microscopes (TEM’s) work
- A beam of electrons passes through a thin section of a specimen.
- Areas that absorb the electrons (denser areas) appear darker on the electron micrograph that is produced (as the electrons don’t pass through)
- The electron beam is focused by electromagnets inside a vacuum environment.
How do Scanning Electron Microscopes (SEM’s) work
- A beam of electrons passes across the surface and scatter.
- The pattern of scattering builds up a 3D image depending on the contours of the specimen.
What are some advantages of electron microscopes
- Higher magnification and resolution than light microscopes (electrons have a shorter wavelength).
- Can therefore see smaller structures like ribosomes.
- SEM produces a 3D image.
What are some disadvantages of electron microscopes
- Whole system must be in a vacuum so living specimen cannot be observed.
- A complex staining process is required which could introduce artefacts into the image.
- Specimen must be very thin, especially for TEM, so that electrons can pass through.
What are 5 key features of eukaryotic cells
- DNA contained in a membrane-bound nucleus (surrounded by a membrane).
- DNA tightly wrapped around proteins called histones. The DNA and histone proteins form chromosomes.
- DNA is a linear molecule ( ends of chromosomes not joined in a loop).
- Contain membrane-bound organelles, e.g. mitochondria
- Contain 80s ribosomes.
Describe the structure of the nucleus
- Surrounded by the nuclear envelope - a double membrane which controls the entry/ exit of materials and contains reactions within the nucleus.
- The nuclear envelope has nuclear pores - allows the passage of large molecules.
- Bulk of the nucleus is made of nucleoplasm - a granular, jelly-like material.
- Nucleolus in the centre - manufactures ribosomal RNA (rRNA) and assembles ribosomes.
What are the functions of the nucleus
- Controlling the cell’s activities - the DNA contains instructions to produce proteins.
- Synthesis of ribosomes - the nucleolus makes ribosomal RNA.
- Exchange between nucleus and cytoplasm - Substances can enter or leave the nucleus via the nuclear pores.
Describe the structure of the cell-surface membrane
- Phospholipid bilayer.
- Mainly made up of lipids and proteins.
What are the functions of the cell-surface membrane
- Controlls movement of substances into and out of the cell - the membrane is partially permeable.
- Cell signalling - receptors can detect signals from other cells.