TY - JOUR
T1 - Shotgun immunoproteomics to identify disease-associated bacterial antigens
T2 - Application to human colon cancer
AU - Tjalsma, Harold
AU - Lasonder, Edwin
AU - Schöller-Guinard, Marie
AU - Swinkels, Dorine W.
PY - 2007/4/1
Y1 - 2007/4/1
N2 - Circulating antibodies reflect a mirror view of invading antigens that are related to infection and cancer. This was recently exemplified by using serum antibodies to capture Streptococcus bovis antigens followed by MS to generate antigen profiles that were diagnostic for colon cancer. These bacterial antigen profiles have a high potential to aid in the immuno-diagnosis of this disease, as the magnitude of the immune response to bacterial antigens is, in general, superior to the immune response against tumor (self) antigens. In this study, the identity of individual colon cancer-associated streptococcal antigens was revealed by enrichment of these "diagnostic" antigens by selected patient antibodies followed by high-accuracy nanoLC-MS/MS peptide identification. This showed that both the histone-like protein HIpA and the ribosomal protein Rp L7/L12 are members of the colon cancer-associated S. bovis immunome. Both antigens also seem to belong to the group of anchorless surface proteins, like 14 additional proteins that were co-identified in S. bovis cell wall extracts. Among these were the known streptococcal anchorless surface proteins GAPDH and Enolase. Taken together, these data show that shotgun immunoproteomics, combining immunocapture in-line with LC MS/MS, is a convenient approach for the rapid identification of disease-associated bacterial antigens.
AB - Circulating antibodies reflect a mirror view of invading antigens that are related to infection and cancer. This was recently exemplified by using serum antibodies to capture Streptococcus bovis antigens followed by MS to generate antigen profiles that were diagnostic for colon cancer. These bacterial antigen profiles have a high potential to aid in the immuno-diagnosis of this disease, as the magnitude of the immune response to bacterial antigens is, in general, superior to the immune response against tumor (self) antigens. In this study, the identity of individual colon cancer-associated streptococcal antigens was revealed by enrichment of these "diagnostic" antigens by selected patient antibodies followed by high-accuracy nanoLC-MS/MS peptide identification. This showed that both the histone-like protein HIpA and the ribosomal protein Rp L7/L12 are members of the colon cancer-associated S. bovis immunome. Both antigens also seem to belong to the group of anchorless surface proteins, like 14 additional proteins that were co-identified in S. bovis cell wall extracts. Among these were the known streptococcal anchorless surface proteins GAPDH and Enolase. Taken together, these data show that shotgun immunoproteomics, combining immunocapture in-line with LC MS/MS, is a convenient approach for the rapid identification of disease-associated bacterial antigens.
KW - Colon cancer
KW - Immunocapture mass spectrometry
KW - Immunoproteomics
KW - MS
KW - NanoLC-MS
KW - Streptococcus bovis
UR - http://www.scopus.com/inward/record.url?scp=38149103497&partnerID=8YFLogxK
U2 - 10.1002/prca.200601018
DO - 10.1002/prca.200601018
M3 - Article
AN - SCOPUS:38149103497
VL - 1
SP - 429
EP - 434
JO - Proteomics - Clinical Applications
JF - Proteomics - Clinical Applications
SN - 1862-8346
IS - 4
ER -