TY - JOUR
T1 - Standardized sample preparation phases for a quantitative measurement of plasma peptidome profiling by MALDI-TOF
AU - D'Imperio, Marco
AU - Della Corte, Anna
AU - Facchiano, Angelo
AU - Di Michele, Michela
AU - Ferrandina, Gabriella
AU - Donati, Maria B.
AU - Rotilio, Domenico
PY - 2010/5/7
Y1 - 2010/5/7
N2 - A growing body of literature defines MALDI-TOF MS as a technique for studying plasma and serum, thus enabling the detection of proteins, and the generation of reproducible protein profile mass spectra, potentially able to discriminate correctly different biological systems. In this work, the different steps of the pre-analytical phase that may affect the reproducibility of plasma proteome analysis have been carefully considered. The results showed that the method is highly accurate (9.1%) and precise (8.9%) and the calibration curve for the ACTH (18-39), in human plasma, gave a good correlation coefficient (r > 0.99 and r2 > 0.98). The limit of detection (LOD) and the limit of quantification (LOQ), relative intensity, were of 0.5 × 10-9 M and 1.0 × 10-9 M respectively. Thus, an assay has been developed for the detection of low-abundant and low molecular weight proteins, from human plasma, aiming at the identification of new potential biomarkers. The method was tested on plasma from patients with a first diagnosis of pelvic mass. Statistical analysis of plasma profile generated a sub-profile of 17 peptides with their relative abundance able to discriminate patients bearing malignant or benign tumors. The sensitivity and specificity were 85.7% and 80.0% respectively.
AB - A growing body of literature defines MALDI-TOF MS as a technique for studying plasma and serum, thus enabling the detection of proteins, and the generation of reproducible protein profile mass spectra, potentially able to discriminate correctly different biological systems. In this work, the different steps of the pre-analytical phase that may affect the reproducibility of plasma proteome analysis have been carefully considered. The results showed that the method is highly accurate (9.1%) and precise (8.9%) and the calibration curve for the ACTH (18-39), in human plasma, gave a good correlation coefficient (r > 0.99 and r2 > 0.98). The limit of detection (LOD) and the limit of quantification (LOQ), relative intensity, were of 0.5 × 10-9 M and 1.0 × 10-9 M respectively. Thus, an assay has been developed for the detection of low-abundant and low molecular weight proteins, from human plasma, aiming at the identification of new potential biomarkers. The method was tested on plasma from patients with a first diagnosis of pelvic mass. Statistical analysis of plasma profile generated a sub-profile of 17 peptides with their relative abundance able to discriminate patients bearing malignant or benign tumors. The sensitivity and specificity were 85.7% and 80.0% respectively.
KW - Accuracy
KW - Biomarkers
KW - LOD-LOQ
KW - MALDI-TOF MS
KW - Plasma profile
KW - Precision
UR - http://www.scopus.com/inward/record.url?scp=77950918062&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=77950918062&partnerID=8YFLogxK
U2 - 10.1016/j.jprot.2010.03.001
DO - 10.1016/j.jprot.2010.03.001
M3 - Article
C2 - 20227539
AN - SCOPUS:77950918062
SN - 1874-3919
VL - 73
SP - 1355
EP - 1367
JO - Journal of Proteomics
JF - Journal of Proteomics
IS - 7
ER -