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Biochemistry 300 Introduction to Structural Biology

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Title: Biochemistry 300 Introduction to Structural Biology


1
Biochemistry 300Introduction to Structural
Biology
Jan. 10, 2007
  • Walter Chazin
  • 5140 BIOSCI/MRBIII
  • E-mail Walter.Chazin_at_vanderbilt.edu
  • http//structbio.vanderbilt.edu/chazin/classnotes/

2
Biology is Organized into Structures
Organ ? Tissue ? Cell ? Molecule ? Atoms
  • A cell is an organization of millions of
    molecules
  • Proper communication between these molecules is
    essential to the normal functioning of the cell
  • To understand communication
    Determine the arrangement of atoms

3
What is Structural Biology?
Sequence
Structural Scales
MESDAMESETMESSRSMYNAMEISWALTERYALLKINCALLMEWALLYIP
REFERDREVILMYSELFIMACENTERDIRATVANDYINTENNESSEEILI
KENMRANDDYNAMICSRPADNAPRIMASERADCALCYCLINNDRKINASE
MRPCALTRACTINKARKICIPCDPKIQDENVSDETAVSWILLWINITALL
polymerase
SSBs
Complexes
helicase
primase
Assemblies
Cell Structures
System Dynamics
4
Atomic Resolution Structural Biology
  • Determine atomic structure to analyze why
    molecules interact

5
The Reward Understanding?Control
Shape
6
Atomic Structure in Context
7
Current Strategy for Atomic Resolution Structural
Biology
  • Break down complexity so that the system can be
    understood at a fundamental level
  • Build up a picture of the whole from the
    reconstruction of the high resolution pieces
  • Understanding basic governing principles enables
    prediction, design, control
  • Pharmaceuticals, biotechnology

8
Build-up Quaternary Structure
70AB
14/32D/70C
X-ray
Zn
B
A
C
D
RPA70 RPA32 RPA14
NTD
NMR
14
CTD
70NTD
32CTD
quaternary structure?
9
Put Structure Into Context
MBP-tagged Siah-1
10
Approaches to Atomic Resolution Structural Biology
  • NMR Spectroscopy X-ray
    Crystallography
  • Computation
  • Determine experimentally or model 3D structures
    of biomolecules
  • ESR/Fluorescence to measure distances when
    traditional methods fail
  • EM/Scattering to get snapshots of whole
    molecular structures
  • (Cryo-EM starts to approach atomic resolution!)

11
Inserting High Resolution Structures Into Low
Resolution Envelopes
Mesh DAMMIN Ribbon 1QUQ
12
Why Structure in silico?
  • A good guess is better than nothing!
  • Enables the design of experiments
  • Potential for high-throughput
  • Crystallography and NMR dont always work!
  • Many important proteins do not crystallize
  • Size limitations with NMR

13
Computational ApproachesMolecular Simulations
  • Convert experimental data into structures
  • Predict effects of mutations, changes in
    environment
  • Insight into molecular motions
  • Interpret structures- characterize the chemical
    properties (e.g. surface) to infer function

14
Computational ApproachesStructure Prediction
  • Secondary structure (only sequence)
  • Homology modeling (using related structure)
  • Fold recognition
  • Ab-initio 3D prediction The Holy Grail

15
Complementarity of theAtomic Resolution Methods
  • X-ray crystallography- highest resolution
    structures faster than NMR
  • NMR- enables widely varying solution conditions
    characterization of motions and dynamic, weakly
    interacting systems
  • Computation- fundamental understanding of
    structure, dynamics and interactions (provides
    the why answers) models without experiment very
    fast

16
Representations of 3D Structures
Both accuracy and precision are important
17
THE STRUCTURE?
  • To correctly represent 3D structure (not a
    model), the uncertainty in each atomic coordinate
    must be represented
  • Polypeptides are dynamic and therefore occupy
    more than one conformation

18
Accuracy/Precision Determined Differently for
X-ray and NMR
19
Variability Uncertainty and Flexibility in
Experimental Structures
20
Representation of Structure Conformational
Ensemble
  • Neither crystal nor solution structures can be
    properly represented by a single conformation
  • Intrinsic motions
  • Imperfect data

Variability reflected in the RMSD of the ensemble
21
Challenges For Understanding The Meaning of
Structure
  • Structures determined by NMR, computation, and
    X-ray crystallography are static snapshots of
    highly dynamic molecular systems
  • Biological process (recognition, interaction,
    chemistry) require molecular motions (from
    femto-seconds to minutes)
  • New methods are needed to comprehend and
    facilitate thinking about the dynamic structure
    of molecules visualization

22
Visualization of Structures
Intestinal Ca2-binding protein!
  • Need to incorporate 3D and motion

23
Center for Structural Biology
Dedicated to furthering biomedical research and
education involving 3D structures at or near
atomic resolution http//structbio.vanderbilt.edu
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