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Spectroscopy

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Spectroscopy
Light is an electric and magnetic field and has wave like and particle like properties (quanta)
- Speed(c)=3 billion m/s
- Frequency=c/wavelength
- Speed(c)=3 billion m/s
Energy=Planks constant(6.62*10^-32Js)* Frequency
- Longer wavelength means lower energy
- WAVE NUMBER(cm-1)= 1/wavelength(m or nm)
- Infared has lower energy than ultraviolet
- Ground state to excited state= E1-->E2, this has discrete intervals (at some frequencies there is no absorption)
- There are different energy levels
- Vibrational
- There is stretching and bending
- This is in the infared part of the spectrum
- Rotational
- Single covalent bonds can rotate
- Energy increments here are smaller than vibrational so correspond to microwave part
- electron spin orientation
- Microwaves also change electron spin
- Nuclear spin orientation
- Related to radio waves
- Vibrational
- Longer wavelength means lower energy
x-rays cause electrons to jump from ground state and is then ejected
INFARED
- The C=O may stretch and bend ( stretching occurs at 1600cm-1 and bending at 800cm-1), these may cause differences in bond length and angle. There are also twisting vibrations (happens between torsion angles-phi/psi)
- The more bonds there are the lower the frequency, so a double bond has a low frequency
- An infared plot is absorbance versus frequency/ wave number
- Water gives a strong absorption so need to be removed it is replaced by deuterated water which replaces H with D which is much heavier. You can also just do it in an non aqueous solution (dry films) or a KBr disk
- As it can study non aqueous solutions insoluble membrane proteins can also be studied
- The protein should be 10mg/ml, 10 microlitre path length
- Can identify is prion protein has been mutated as the mutated form is a insoluble and has a b-sheet structure opposed to it's original a-helix
- Water gives a strong absorption so need to be removed it is replaced by deuterated water which replaces H with D which is much heavier. You can also just do it in an non aqueous solution (dry films) or a KBr disk
- Most infrared of a protein comes from its backbone producing different AMIDE BANDS which are associated with the hydrogen bonds
- Amide band 1-associated with stetching of c=o -1690 to1600cm-1
- Amide band 2- due to N-H (1575-1480cm-1) bending and C-H stretching (1575-1480cm-1)
- The peak postions depend on the 2 structure
- a-helix-1648-1657cm-1
- b-sheet:1640-1620cm-1)
- Amide A- due to N-H stretch (3300-3100cm-1)
- Amide bands measure the secondary structure , FTIR measures the different structures.
- The IR spectra has a helix accuracy of +/- 4% and b-sheet accuracy of +/-8%
- The picture shows a Michelson interferometer ot FTIR
- The crystal will transmit half the light and reflect the other half- this is the BEAM SPLITTER. This is parallel to a mirror. There is also a moving mirror where the trasmitted beam shines. The beams reflected by the mirrors combine to make a RESULTANT BEAM
- If the 2 beams are in phase it will make constructive interferance , if they're not it will be destructive
- The crystal will transmit half the light and reflect the other half- this is the BEAM SPLITTER. This is parallel to a mirror. There is also a moving mirror where the trasmitted beam shines. The beams reflected by the mirrors combine to make a RESULTANT BEAM
UV also called Electron absorption spectroscopy
- A SPECTROPHOTOMETER measures UV. A deutrium light source is needed for UV, a tungsten halogen lamp is needed for UV in the vsible range. A MONOCHROMATER scans the wavelengths from the lamp to select ONE, this is a DIFFRACTION GRATING.Transmitted light then goes to the photodetector which coverts light intensity to an elctrical signals by amplifying it
- The cuvette with the sample should be made of quarts glass if absorbing UV
- Incident light is light before it hits the sample
- Transmittance=Transmitted light/Incident light
- Absorbance=log10 1/transmittance
- If the absorbance is below 1 it is very dark. If the absorbance is between 1 and 1.5 it's a good sample
- BEER LAMBERT LAW: Extinction coefficient(M-1cm-1)* concentration(Molar) *Path length (usually 1cm)
- The extinction coefficient can usually be found as the slope on a graph of absorbance against concentration
- The exctinction coefficent at 280nm= total of them for tryptophan, Tyrosine and disulphide bonds
- The extinction coefficient can usually be found as the slope on a graph of absorbance against concentration
- Absorbance=log10 1/transmittance
- A SPECTROPHOTOMETER measures UV. A deutrium light source is needed for UV, a tungsten halogen lamp is needed for UV in the vsible range. A MONOCHROMATER scans the wavelengths from the lamp to select ONE, this is a DIFFRACTION GRATING.Transmitted light then goes to the photodetector which coverts light intensity to an elctrical signals by amplifying it
Fluorescence
- Light is absorbed and then emmitted
- Electrons go from an excited to ground state
- The emmisions have longer wavelengths than excitations and the energy gap is smaller
- PHOSPHORESCENCE=emission from a triplet excited state,
- Light is absorbed and then emmitted
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- Techniques for biological... Mindmap am Spectroscopy, erstellt von Olivia Alexander am 02/10/2018.
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