TY - JOUR
T1 - Automated mass spectrometry-based functional assay for the routine analysis of the secretome
AU - Wetie, Armand G.Ngounou
AU - Sokolowska, Izabela
AU - Woods, Alisa G.
AU - Wormwood, Kelly L.
AU - Dao, Su
AU - Patel, Sapan
AU - Clarkson, Bayard D.
AU - Darie, Costel C.
N1 - Funding Information:
The authors disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work was supported in part by Clarkson University (start-up to C.C.D.), the Army Research Office through the Defense University Research Instrumentation Program (DURIP grant #W911NF-11-1-0304 to C.C.D.) and Keep A Breast Foundation (KEABF-375-35054).
PY - 2013/2
Y1 - 2013/2
N2 - The secretome represents the set of proteins secreted into the extracellular space of cells. These proteins have been shown to play a major role in cell-cell communication. For example, recent observations revealed the presence of diffusible factors with proliferative properties in the secretome of cancer cells. Thus, a qualitative and quantitative analysis of the secretome could lead to the identification of these factors and consequently to the development of new therapeutic strategies. Here, we provide an automated simple and effective strategy to identify novel targets in the secretome of specifically treated cells using liquid chromatography-tandem mass spectrometry (LC-MS/MS). Furthermore, we explore the supportive role of mass spectrometry (MS) in the development of functional assays of identified secreted target molecules. Simplicity is achieved by growing cells in medium free of serum, which eliminates the need to remove the most abundant serum proteins and at the same time reduces disturbing matrix effects. Upon identification of these factors, their validation and characterization will follow. Moreover, this approach can also lead to the identification of proteins abnormally secreted, shed, or oversecreted by cells as response to a stimulus. Furthermore, we also discuss the problems that one may encounter. Finally, we discuss the broad application of automated MS-based proteomics, particularly in cancer research, highlighting new horizons for the use of MS.
AB - The secretome represents the set of proteins secreted into the extracellular space of cells. These proteins have been shown to play a major role in cell-cell communication. For example, recent observations revealed the presence of diffusible factors with proliferative properties in the secretome of cancer cells. Thus, a qualitative and quantitative analysis of the secretome could lead to the identification of these factors and consequently to the development of new therapeutic strategies. Here, we provide an automated simple and effective strategy to identify novel targets in the secretome of specifically treated cells using liquid chromatography-tandem mass spectrometry (LC-MS/MS). Furthermore, we explore the supportive role of mass spectrometry (MS) in the development of functional assays of identified secreted target molecules. Simplicity is achieved by growing cells in medium free of serum, which eliminates the need to remove the most abundant serum proteins and at the same time reduces disturbing matrix effects. Upon identification of these factors, their validation and characterization will follow. Moreover, this approach can also lead to the identification of proteins abnormally secreted, shed, or oversecreted by cells as response to a stimulus. Furthermore, we also discuss the problems that one may encounter. Finally, we discuss the broad application of automated MS-based proteomics, particularly in cancer research, highlighting new horizons for the use of MS.
KW - LC-MS/MS
KW - MALDI-MS
KW - Mass spectrometry
KW - Posttranslation modifications
KW - Secretome
UR - https://www.scopus.com/pages/publications/84878326517
U2 - 10.1177/2211068212454738
DO - 10.1177/2211068212454738
M3 - Article
C2 - 22853965
AN - SCOPUS:84878326517
SN - 2211-0682
VL - 18
SP - 19
EP - 29
JO - Journal of laboratory automation
JF - Journal of laboratory automation
IS - 1
ER -