Protein Structure

Lecture 7 Video 6

๐Ÿงฌ Lecture 7 โ€” Video 6 Summary

(Protein crystallography: symmetry, diffraction geometry & data statistics)


๐Ÿ”ท 1. Recap: Unit Cell โ€” The โ€œBuilding Blockโ€ of Crystals

A unit cell is the smallest repeating box that builds the entire crystal.

It is defined by 6 parameters:

  • 3 unit cell lengths:
    • ( a, b, c )
  • 3 interaxial angles:
    • ( alpha, eta, gamma )

Crystal Systems (7 total)

They range from least constrained โ†’ most constrained:

SystemConstraints
TriclinicNo constraints
MonoclinicOne angle fixed
OrthorhombicAll angles = 90ยฐ
TetragonalAngles 90ยฐ, a=b
Trigonal / HexagonalSpecial rotational symmetry
CubicAll angles 90ยฐ, a=b=c

๐Ÿ”ท 2. Bravais Lattices (14 total)

Beyond just corners, lattices can have additional centering:

  • Primitive (P) โ†’ lattice points only at corners
  • Body-centered (I) โ†’ extra point in the middle
  • Face-centered (F) โ†’ points on each face
  • Base-centered (C) โ†’ points on one pair of faces

These combinations give 14 Bravais lattices.


๐Ÿ”ท 3. Symmetry Operations in Protein Crystals

Three major symmetry operations:

๐ŸŸข Translation

Move the molecule without rotating.

๐Ÿ”ต Rotation

Rotate around an axis:

  • 2-fold
  • 3-fold
  • 4-fold
  • 6-fold

๐ŸŸฃ Screw Axis

Rotation + translation along axis

Example:

  • 4โ‚ screw โ†’ rotate 90ยฐ and translate ยผ unit cell.

๐Ÿ”ท 4. Space Groups โ€” Why Only 65 for Biomolecules?

Mathematically:

  • 230 total space groups

But proteins only use 65.

Reason: Chirality

  • Proteins contain L-amino acids
  • Mirror symmetry or inversion would create D-amino acids
  • This cannot happen in real protein crystals

Therefore: ๐Ÿ‘‰ Only non-inverting symmetry space groups are allowed.


๐Ÿ”ท 5. What Do You Need to Describe a Crystal Structure?

Three key things:

  1. Atomic structure of the asymmetric unit (e.g., one protein molecule)
  2. Unit cell dimensions
  3. Space group symmetry

By applying symmetry operations to the asymmetric unit โ†’ You reconstruct the entire crystal lattice.


๐Ÿ“ก 6. Diffraction Geometry โ€” Braggโ€™s Law

When X-rays hit parallel crystal planes:

Constructive interference occurs when:

2dsin heta = lambda

Where:

  • d โ†’ distance between crystal planes
  • ฮธ โ†’ Bragg angle
  • ฮป โ†’ X-ray wavelength

This condition produces visible diffraction spots.


๐Ÿ”ท Miller Indices (hkl)

They define which plane diffracts.

Example in lecture:

  • Plane intersects:
    • a-axis once โ†’ h = 1
    • b-axis twice โ†’ k = 2
    • c-axis twice โ†’ l = 2

So plane = (1 2 2).


๐ŸŒ 7. The Ewald Sphere โ€” When Diffraction Happens

Important conceptual tool:

  • Virtual sphere with radius ( 1/lambda )
  • Crystal sits at center
  • Reciprocal lattice rotates as crystal rotates

Diffraction condition:

๐Ÿ‘‰ A diffraction spot appears when a reciprocal lattice point touches the Ewald sphere.

As the crystal rotates โ†’ different reciprocal lattice layers (โ€œlunesโ€) intersect โ†’ new reflections recorded.


๐Ÿ“Š 8. Understanding โ€œTable 1โ€ in Crystallography Papers

This table shows data quality statistics.


๐Ÿงฉ Space Group & Unit Cell

Example:

  • P2โ‚2โ‚2โ‚ โ†’ primitive lattice + three 2-fold screw axes
  • Orthorhombic โ†’ angles = 90ยฐ (often not listed)

Unit cell lengths shown in ร…ngstrรถm.


๐ŸŽฏ Resolution

  • Example datasets:
    • 3.4 ร… (lower resolution)
    • 1.9 ร… (higher resolution โ†’ better detail)

โ€œLast shellโ€ = highest resolution range used in statistics.


๐Ÿ“‰ R-merge

Measures consistency between repeated measurements.

  • Lower = better
  • Typically increases in last shell (~0.5)

High resolution dataset โ†’ usually lower R-merge overall.


๐Ÿ”Š Signal-to-Noise (I/ฯƒI)

Rule of thumb:

  • Cut data when I/ฯƒI โ‰ˆ 2

Example:

  • Overall: 8.5
  • Last shell: 1.6 โ†’ borderline

Better dataset:

  • Overall: 26
  • Last shell: 2.9 โ†’ strong data.

โœ… Completeness

How many possible reflections were measured.

  • Ideal: ~100%
  • Even ~80% can still give good electron density maps

But always aim for highest completeness.


๐Ÿ” Redundancy (Multiplicity)

How many times each reflection was measured.

  • Good target: >3
  • Example: ~6 โ†’ very good statistics.

โญ Key Big-Picture Takeaways

  • Protein crystals are defined by unit cell + symmetry + asymmetric unit
  • Only 65 space groups are possible due to chirality
  • Diffraction happens when Braggโ€™s law is satisfied
  • The Ewald sphere explains diffraction geometrically
  • Always check Table 1 in papers to judge structure quality:
    • Resolution
    • R-merge
    • I/ฯƒI
    • Completeness
    • Redundancy

Quiz

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