Naslov
Protein analysis by mass spectrometry

Autori
Galić, Nives

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni

Izvornik
7th International Symposium and Summer School on Bioanalysis / - Pečuh, 2007

Skup
7th International Symposium and Summer School on Bioanalysis

Mjesto i datum
Pečuh, Mađarska, 10.06.2007. - 15.06.2007

Vrsta sudjelovanja
Pozvano predavanje

Vrsta recenzije
Nije recenziran

Ključne riječi
mass spectrometry; protein analysis; sequence analysis

Sažetak
Soft ionization techniques, electrospray (ESI) and matrix-assisted laser desorption/ionization (MALDI) have partly supplemented, partly replaced traditional techniques for the identification and structural analysis of biological macromolecules. Mass spectrometry (MS) is used for determination of the molecular weight of peptides and protein, sequence analysis, characterization of protein-ligand interactions etc. The detection limit, resolution and mass accuracy depend on instrument used. Impurities (buffers, salts, detergents) can reduce the ion intensities or even totally suppress them, so a separation method (chromatography, 2D-gel electrophoresis) must be used for purification of the sample. Molecular weight of intact protein can be determined by ESI or MALDI MS. Multiply charged ions are produced by ESI MS, while singly charged ions are predominant in MALDI spectra. Sequence analysis of proteins by MS can be performed using peptide mass fingerprint. In this method, proteins are separated by 2-D gel electrophoresis and digested with specific protease or digested and then separated by twodimensional chromatography. The obtained peptide mixtures are analyzed by MS or MALDI-TOF technique. The masses determined by MS are compared with calculated masses from database entries. Different algorithms have been developed for protein identification. It is known that detection of peptides by MS is influenced by intrinsic properties like amino acid composition, the basicity of the C-terminal amino acid, hydrophobicity, etc. Arginine-containing peptides dominate in MS spectra of tryptic digest, so the chemical derivatization of lysine terminal residue by O-methilisourea or 2-methoxy-4, 5-1H-imidazole was suggested. The peptide mass fingerprint method can be improved further by peptide fragmentation using tandem mass spectrometry (collision-induced dissociation, CID or post-source decay, PSD). Since any of the peptide bonds can be broken in several ways, the MS/MS spectra are complex, and quite difficult to interpret. Chemical derivatization is used to obtain only or predominantly one type of fragment ions. Sulfonation of N-terminal amino group enhance PSD sequencing, producing mainly y-type fragment ions. The mass difference of two consecutive y-ions corresponds to an amino acid mass, so the peptide sequence can be obtained with minimal or no assistance from genomic data, e.g. de novo protein sequencing is possible.

Izvorni jezik
Engleski

Znanstvena područja
Kemija

POVEZANOST RADA