Acknowledgements: We thank the LSMBO and the Structural Biology and Genomics Dept. members. This work was supported by funds from SPINE EEC QLG2-CT-2002-00988, FNS through the Genopole program, CNRS, INSERM, ULP and local authorities (Region of Alsace, Department of Bas-Rhin and city of Strasbourg).

Native and Denaturing Mass Spectrometry (MS) in the context of Structural Genomics

H. Nierengarten1,2, M. Ruff1, A. Poterszman1, I. Billas1, N. Rochel1, N. Potier3, M. Argentini2, S. Sanglier3, J.C. Thierry1, D. Moras1, A. Van Dorsselaer3

1 Structural Biology and Genomics Dept., IGBMC, Illkirch, France 2. MALDI-TOF Facility IGBMC, Illkirch Strasbourg, France3. Dept. of Bio-Organic Mass Spectrometry (LSMBO), Strasbourg, FRANCE

The two main mass spectrometers dedicated to the study of proteins of the IGBMC proteomic open platform:

2) The MALDI-TOF mass spectrometer (Reflex IV, Bruker) to identify proteins by peptide mass finger printing.

1)The ESI-TOF mass spectrometer (Micromass, Waters) for native (physiologic conditions) and denaturing (acidic conditions) MS studies.

1) Denaturing Mass Spectrometry (molecular MS)

2) Native Mass Spectrometry (supramolecular MS)

Abstract: The use of molecular MS, for the characterization of biomacromolecules is now well established: MALDI-MS and ESI-MS under denaturing conditions provide information on the molecular masses, on the purity and on primery sequences of proteins. More recently, thanks to the gentle nature of the ESI process, specific non-denaturing ESI (native or supramolecular MS) protocols have been developed to detect and investigate non-covalent interactions (i.e. secondary, tertiary, and quaternary structures of protein complexes). In the field of Structural Genomics at IGBMC, MS is now routinely used to assist structure determinations through each stage of the process of protein crystallography or NMR. Here, we summarize the multiple possibilities of Denaturing and Native MS in a Structural Genomics context.

5 pmol/L( H2O:CH3CN, 1% HCOOH)

active conformation is lost

only covalent interactions

are detected

20 pmol/L( NH4OAc 20-50 mM, physiological pH)

Native conformation is kept (active form)

non-covalent complexes

are detected

-Characterize (in terms of sequence integrity) and evaluate the purity (or homogeneity) of protein (or oligonucleotide) preparations to verify that the desired protein construct has been correctly expressed. If the molecular weight is not in agreement with the theoretical one, the protein is analyzed by MALDI-MS to identify the unexpected modification and/or deletion using peptide mass finger printing.

-Direct identification of macromolecular crystal content not easely detectable by other classical techniques to verify if the protein has crystallized with all its expected partners [1].

-Verify the successful incorporation of seleno-methionine (see exemple 1) or stable isotopes (N15C13)

-Characterization and study of specific protein/protein, protein/ ligand, protein/peptide, protein/DNA, protein/metal non-covalent complexes……..

-Screening libraries of ligands.

-Determination of the stoichiometry of interaction.

-Detection of fortuitous ligands captured during expression and/or purification (see exemple 2). [2]

b) Ex 1: denaturing ESI-MS to test the incorporation of 4 seleno-methionine ( 50% CH3CN, 1% HCOOH)

b) Ex 2: detection of an unexpected ligand in a NR using denaturing and native ESI-MS

!Sample preparation: The sample preparation is one of the key step for a good MS result. Prior to any mass analysis, the sample has to be desalted (generally on centricon micro-concentrtors) against ammonium acetate. Ammonium acetate enables native structures of proteins to be preserved and is compatible with ESI-MS analyses. Typically between 3 and 6 dilution/concentration steps are performed. After desalting, the protein is diluted to 5 pmol/L in a 1:1 water-acetonitrile mixture acidified with 1% formic acid for a denaturing MS experiment . For native experiments, samples are diluted to 20 pmol/L in ammonium acetate (20-50 mM, pH = 6.8).

a) Possibilities of denaturing MS in a structural genomics context ?

a) Possibilities of native MS in a structural genomics context ?

0

1 0 0

%

1 6 +

1 8 +

1 9 +

2 0 +

1 5 +

1 4 +

1 3 +

1 2 +1 1 +

9 +1 0 +

1 7 +

5 0 0 2 1 0 0m / z0

1 0 0

%

1 6 +

1 8 +

1 9 +

2 0 +

1 5 +

1 4 +

1 3 +

1 2 +1 1 +

9 +1 0 +

1 7 +

5 0 0 2 1 0 0m / z

0

1 0 0

%

5 0 0 2 1 0 0m / z

1 6 +

1 8 +

1 9 +

2 0 +

1 5 +

1 4 +

1 3 +

1 2 +1 1 +

9 +1 0 +

1 7 +

0

1 0 0

%

5 0 0 2 1 0 0m / z0

1 0 0

%

5 0 0 2 1 0 0m / z

1 6 +

1 8 +

1 9 +

2 0 +

1 5 +

1 4 +

1 3 +

1 2 +1 1 +

9 +1 0 +

1 7 +

A: 17263.2 ± 0.6 Da

B: 17451.6 ± 0.7 Da

Spectrum of theh Native (Met) protein

Spectrum of the protein that has incorated seleno-methionines

MW (Met) = 131.2 DaMW (Se-Met) = 178.1 Da

46.9 Da

= + 188.4 Da ( = 4 x 46.9 Da )

The mass difference indicates a total

incorporation of the Se-Met

[1]. Characterization of crystal content by ESI-MS and MALDI-MS, Acta Crystallogr D Biol Crystallogr, 2000 12:1583-90.[2]. Using nondenaturing MS to detect fortuitous ligands in orphan nuclear receptors, Protein Sci., 2003 12(4):725-33.

A : 34419 ± 1 Da

1000 1500 2000 2500 3000 3500m /z0

100

%

A12+

A20+

1000 1500 2000 2500 3000 3500m /z0

100

%

A12+

A20+

2000 2200 2400 2600 2800 3000 3200 3400m /z0

100

%

B13+

B12+

A14+

A13+

A12+

2000 2200 2400 2600 2800 3000 3200 3400m /z0

100

%

B13+

B12+

A14+

A13+

A12+

Denaturing conditions(50% CH3CN, 1% HCOOH): only one compound is detected

Non-denaturing conditions (25 mM AcONH4, pH 6.8):two species are detected

A: 34419 ± 2 DaB : 34706 ± 4 Da

M ~ 287 ± 8 Da A: 34419 ± 2 DaB : 34706 ± 4 Da

M ~ 287 ± 8 Da

~50% of the NR has non covalently fixed an unexpectedmolecule ( ) of ~ 287 Da !

~50% of the NR has non covalently fixed an unexpectedmolecule ( ) of ~ 287 Da !

By comparing the spectra obtained under denaturing conditions (protein is unfolded and non-covalent interactions between molecules are lost) and under native conditions (protein is folded and weak interactions are maintained) It is possible to conclude that the extra mass of 287 Da is due to a non-covalent attachment of a fortuitous small ligand.