By Rambo and Tainer

Post on 19-Jan-2016

33 Views

Category:

Documents

1 Downloads

Preview:

Click to see full reader

DESCRIPTION

Bridging the solution divide: comprehensive structural analyses of dynamic RNA, DNA, and protein assemblies by small-angle X-ray scattering. By Rambo and Tainer. Introduction. Importance of development of techniques that probe nucleic acid or protein-nucleic acid complex - PowerPoint PPT Presentation

Transcript

Bridging the solution divide: comprehensive structural analysesof dynamic RNA, DNA, and protein

assemblies bysmall-angle X-ray scattering

By Rambo and Tainer

Introduction

• Importance of development of techniques that probe nucleic acid or protein-nucleic acid complex

• Three Predominant Techniques Used in Structural Biology– Macromolecular X-ray Crystallography (MX)– Nuclear Magnetic Resonance (NMR)– Electron Microscopy (EM)

• These techniques have limitations for macromolecules with functional flexibility and intrinsic disorder

2

Instrumentation

3

Sample Preparation

• Stresses high purity, high homogeneity similar to crystallography

• Amount needed is 15 μL with protein concentration ranging from 0.1- 10 mg/ml.

• Typically 2-5 mg/ml is best higher concentration yields better signal but can lead to aggregation

4

SAXS Theory

• Three things to examine – SAXS profile in

reciprocal and real space

– Gunier Plot (not shown)

– Kratky Plot

5

SAXS Profile

• Transformation of the scattering data I(q) yield P(r) a histogram of interatomic vectors

• Calculate a structure based on a atomic resolution macromolecular structure

6

Idealized Data

• Measurements at different range of concentration

• X-ray sensitivity can be detected by changes in scattering by repeat exposures

7

Real Data

• Raw shattering curves for all samples. 1st exposure.

• See that with increasing concentration, sample is increased. Better signal at high concentration.

804/21/23

Guinier Plot

• Non linear dependence of log(I(q)) indicates presence of aggregation

• Presence of aggregation means no data

9

Gunier Real Data

04/21/2310

Radius of Gyration

• Radius of gyration is calculated by taking I(0) at q= 0.

• Needs to be compared against a set of standards

11

Interparticle Interference

• Increasing concentration can reveal concentration dependence

• Visible in decrease in intensity at small q.

12

P(r) Distribution in Real Space

• From this distribution you can tell two things– Dmax– Some general

information about shape

13

Real Data

14

Dmax = 110Dmax = 115

Kratky Plot

• Kratky plot also is an indication of protein folding/ unfolding

• Globular proteins macromolecules follow Porod’s law and are bell shaped

15

Kratky Plot Real Data

04/21/2316

No Atomic Structure

• Without previously known structure can still make shape prediction

• Programs such as GASBOR and DAMMIF allow for low resolution structure

17

Atomic Structure Solved

• Calculate curve from known data and compare to experimental data

• Disagreement– Investigate alternate

states– Investigate mixture

of states– Investigate flexibility

18

Gasbor Ub-PCNA

Conformation Assembly

• Use of a variety of software to find best fit

• X2 vs Rg gives good idea about entire ensemble

20

SAM-I: Comparison of Crystal Against SAXS

• Crystal structure was determined in presence of ligand and poorly fit SAXS data

• SAXS guided hypothesis about conformational switching as mechanism

21

Abscisic Acid Hormone Receptor PYR1

• Crystalized with open-lid and closed-lid conformations.

• Crystal contacts show three possible dimers α-α, β-β, α-β

• SAXS profile distinguishes between three conformations.

22

VS Ribozyme Solution Structure

• Ab initio modeling which lead to identificaiton of helical regions based on helical secondary structure

• Resulting model was converted to residue specific model

23

Erp72 Solution Structure

• Parts previously solved by NMR and MX but solution structure unknown

• Ab initio modeling allowed for putting together of parts into correct orientation in solution

24

p53-Taz2-DNA complex

• Parts had been solved previously – Core and

tetramerization solved by MX

– Taz2 by NMR

• Used in rigid body analysis and protein with and without DNA to model

25

Future of SAXS

• Data analysis are contuining to be developed computational tools

• Synchotron-based facilities can extend SAXS into high throughput region

• Can answer fundamental questions in DNA repair, modeling of large multidomain macromolecular machines and suggests flexibility are criticical for biological funcitions.

26

Questions?

Froliche Weinachten!

(Merry Christmas in German)

27

top related