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From Proteopedia

Revision as of 04:28, 31 March 2011

Introduction

NMR Versus X-Ray Crystallography

The two predominant methods of protein tertiary structure determination are X-Ray Crystallographyand Nuclear Magnetic Resonance(NMR) Spectroscopy.

X-Ray Diffration pattern of a crystallized SARS protease at 2.1 Angstrom resolution.

X-Ray Crystallography entails protein purification, crystallization of the protein, collection of X-Ray diffraction data, calculation of the protein’s electron density relative to the determined data, and finally fitting the protein’s determined residue sequence into the electron density. Crystallization of the protein often lends itself to being the most challenging aspect of this method. While any size protein can be studied via X-Ray Crystallography and the method is well-established, it is often difficult to perform for membrane proteins and the data received reveals no information about the protein’s hydrogen atoms. Also, an assumption made for X-Ray Crystallographic studies is that the crystallized protein is in a conformation similar to that seen in solution. For more information regarding X-Ray Crystallography please click here.

Bimolecular NMR Spectroscopy involves protein purification, dissolving the protein in a suitable solvent, collecting the NMR data, assigning NMR signals, and finally calculating the protein’s tertiary structure. With NMR, the most difficult step is often correctly assigning NMR signals. Although there is no need to crystallize the protein of interest and most hydrogen atoms are evident, NMR is difficult for proteins that don’t dissolve well in common solvents and works best for small proteins. 1-dimensional, 2-dimensional, and 3-dimensional NMR spectroscopy is readily available; however, 2-dimensional and 3-dimensional NMR is most often used for protein tertiary structure determination. 2D NMR reveals chemical shift correlations between spinnable nuclei such as 1H, 13C, 15N, and 13P, as well as atomic coupling, or proximity correlations via bonding. 3D NMR utilizes this methodology in addition to detection of another nuclear spin phenomenon known as the Nuclear Overhauser Effect(NOE), in which proximity correlations are can be observed in 3D space.

2D COSY NMR spectrum of progesterone.

Due to the complexity of assigning NMR signals to specific protons, the data gathered is usually put into a computer that uses complex computer algorithms to render a protein’s tertiary structure. Even though NMR often requires more prior knowledge of the studied protein’s structural information, the end result is often more telling than that of X-Ray Crystallography. With NMR, one can gain a better insight as to what exactly a folded protein might look like in solution including the protein’s conformational flexibility. An example is the many-conformational structure of bovine pancreatic Ribonuclease seen when the page originally loads. For more information regarding NMR Spectroscopy, click here.

History of NMR Ribonuclease Studies

In 1957, the first work was published examining the structure of bovine pancreatic Ribonuclease using 1-Dimensional 1H NMR by Martin Saunder et al.

In 1988, Udgaonkar et al. used 2-dimensional 1H NMR to study bovine pancreatic Ribonuclease and examined protein folding dynamics, which supported the framework model protein folding mechanism.

NMR Study of Ribonuclease Folding Dynamics

Experimental Prcedure

Using 2-dimensional 1H NMR, Udgaonkar et al. studied the folding pathway of bovine pancreatic Ribonuclease using an exchange reaction between with solvent protons. 2- dimensional 1H NMR allowed for monitoring of proton exchange in the amide backbone for ten second time intervals, and this proton labeling could be terminated via a rapid drop in pH reaction conditions. This research focused on initial protein folding steps.

Starting with denatured wt Ribonuclease, it was suggested that as the peptide began to fold, the backbone amide proteins would become less energetically favorable to exchange protons with the solvent as the backbone amide protons became involved in folding-related intermolecular interactions (such as ).

Data and Results

became evident as those involved in folding-related intermolecular interactions during initial protein folding steps: Those associated with , , , , and . All five of these protons are involved in hydrogen bonding within the of Ribonuclease; therefore, it was believed that this secondary structure was the starting point for the folding mechanism of Ribonuclease. Furthermore, this suggests the formation of a stable secondary structure before the formation of the , which is consistent with the framework model of protein folding mechanisms (in comparison with the jigsaw puzzle model).

References

External Resources

Daniel Kroupa 05:03, 30 March 2011 (IST)