4.7 Article

Identification and characterization of disulfide bonds in proteins and peptides from tandem MS data by use of the MassMatrix MS/MS search engine

Journal

JOURNAL OF PROTEOME RESEARCH
Volume 7, Issue 1, Pages 138-144

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/pr070363z

Keywords

disulfide linkage; tandem mass spectrometry; database searching; proteomics; post-translational modification

Funding

  1. NATIONAL CANCER INSTITUTE [R56CA107106, R01CA107106] Funding Source: NIH RePORTER
  2. NATIONAL CENTER FOR RESEARCH RESOURCES [S10RR023647] Funding Source: NIH RePORTER
  3. NCI NIH HHS [R01 CA107106-02, R01 CA107106, R56 CA107106, CA107106, R01 CA107106-01, R01 CA107106-03, R01 CA107106-04] Funding Source: Medline
  4. NCRR NIH HHS [S10 RR023647-01, S10 RR023647] Funding Source: Medline

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A new database search algorithm has been developed to identify disulfide-linked peptides in tandem MS data sets. The algorithm is included in the newly developed tandem MS database search program, MassMatrix. The algorithm exploits the probabilistic scoring model in MassMatrix to achieve identification of disulfide bonds in proteins and peptides. Proteins and peptides with disulfide bonds can be identified with high confidence without chemical reduction or other derivatization. The approach was tested on peptide and protein standards with known disulfide bonds. All disulfide bonds in the standard set were identified by MassMatrix. The algorithm was further tested on bovine pancreatic ribonuclease A (RNaseA). The 4 native disulfide bonds in RNaseA were detected by MassMatrix with multiple validated peptide matches for each disulfide bond with high statistical scores. Fifteen nonnative disulfide bonds were also observed in the protein digest under basic conditions (pH = 8.0) due to disulfide bond interchange. After minimizing the disulfide bond interchange (pH = 6.0) during digestion, only one nonnative disulfide bond was observed. The MassMatrix algorithm offers an additional approach for the discovery of disulfide bond from tandem mass spectrometry data.

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