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Structural Biology - X-ray Crystallography (part 1)

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Year 2 lecture notes on the topic Protein X-Ray Crystallography, taught by Dr Konstantinos Beis at Imperial College London. Course: Bsc Biochemistry. Module: Structural Biology.

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TITLE Protein X-ray crystallography DATE




Reason for using X-ray crystallography:

Light microscope provide images of objects around
same size of wavelength of light (500nm)


but average size of a protein is -10nm and

an atom is 0.1 nm



:X-rays are used (wavelength 0.1nm(
=




X-ray microscopes are not feasible to make ... use crystallography

Crystallography process




- - -




I.
grow crystal 2.Put in front of X-ray 3. Electron density 4. build protein structure
beam - get diffraction map according map
pattern



AtOM:
nucleus + electrons
↳ v. Small:volume of atom is defined by electron cloud



molecule:
a set of bonded atoms


Crystal:
an ordered array of the same molecule in 3 dimensions


*
Only a
highly purified protein w/ all the same molecules can crystallize

to workout molecular structure, an
X-ray diffraction pattern is needed:
interaction of x-rays with electrons in crystal
https://bynikkib.com

,TITLE DATE




X-ray: a
travelling electromagnetic wave

↳ has electric and magnetic fields at

right angles to each other



Electric field: a
way of describing the electrostatic
force felt by a charged particle due to the
presence/motion of other charged particles


only consider this as it can interact w/ electrons


tells us which will move
way a the
charge


Electrons will scatter (or diffract) X-rays

by a single electron:

side view tOD View


W
In all
directions




by 2 electrons in close proximity:

each orin the structure becomes
a source of x-ray


detector observes scattering pattern
I resultant of scattered waves

added up

diffraction pattern depends on
structure

X-ray scattering by 2 electrons is like the 2-slit experiment:
↳ diffraction of water through gives
2 slits an
unvarying pattern
of peaks and troughs
depends on slit structure (e.g. width)

https://bynikkib.com

, TITLE DATE




Real structure of a whole protein gives a v. complex
diffraction pattern
:knowing how waves add up (like in 2-slit
experiment) will help deduce structure




WAVES
the wave motion is cyclic
sin and cosine waves are horizontal and vertical projections
of a rotating line (aka radius (


the phase angle (0) Indicates the rotated position of
the line (radius)


O is measured:


where 1800: i radians


:I complete cycle 13000): phase angle of 20:25 radians




wave properties




1. Phase shift is
cyclic: crest at
every interval of 24 (2π, kπ, 64) and

trough at every odd i (π, 34, 5T (

2. Amplitude: maximum displacement from x axis



3.
Wavelength: distance between 2 peaks




https://bynikkib.com

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Uploaded on
February 3, 2023
Number of pages
16
Written in
2022/2023
Type
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Professor(s)
Konstantinos beis
Contains
Structural biology - protein x-ray crystallography

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