TY - JOUR
T1 - Membrane proteins of human fetal primitive nucleated red blood cells
AU - Ponnusamy, Sukumar
AU - Zhang, Huoming
AU - Kadam, Priya
AU - Lin, Qingsong
AU - Lim, Teck Kwang
AU - Sandhu, Jaspal Singh
AU - Kothandaraman, Narasimhan
AU - Mahyuddin, Aniza Puteri
AU - Biswas, Arijit
AU - Venkat, Annapoorna
AU - Hew, Choy Leong
AU - Joshi, Shashikant B.
AU - Chung, Maxey Ching Ming
AU - Choolani, Mahesh
PY - 2012/10/22
Y1 - 2012/10/22
N2 - In humans, primitive fetal nucleated red blood cells (FNRBCs) are thought to be as vital for embryonic life as their counterpart, adult red blood cells (adult RBCs) are in later-gestation fetuses and adults. Unlike adult RBCs, the identity and functions of FNRBC proteins are poorly understood owing to a scarcity of FNRBCs for proteomic investigations. The study aimed to investigate membrane proteins of this unique cell type. We present here, the first report on the membrane proteome of human primitive FNRBCs investigated by two-dimensional liquid chromatography coupled with mass-spectrometry (2D-LCMS/MS) and bioinformatics analysis. A total of 273 proteins were identified, of which 133 (48.7%) were membrane proteins. We compared our data with membrane proteins of adult RBCs to identify common, and unique, surface membrane proteins. Twelve plasma membrane proteins with transmembrane domains and eight proteins with transmembrane domains but without known sub-cellular location were identified as unique-to-FNRBCs. Except for the transferrin receptor, all other 19 unique-to-FNRBC membrane proteins have never been described in RBCs. Reverse-transcriptase PCR (RT-PCR) and immunocytochemistry validated the 2D-LCMS/MS data. Our findings provide potential surface antigens for separation of primitive FNRBCs from maternal blood for noninvasive prenatal diagnosis, and to understand the biology of these rare cells.
AB - In humans, primitive fetal nucleated red blood cells (FNRBCs) are thought to be as vital for embryonic life as their counterpart, adult red blood cells (adult RBCs) are in later-gestation fetuses and adults. Unlike adult RBCs, the identity and functions of FNRBC proteins are poorly understood owing to a scarcity of FNRBCs for proteomic investigations. The study aimed to investigate membrane proteins of this unique cell type. We present here, the first report on the membrane proteome of human primitive FNRBCs investigated by two-dimensional liquid chromatography coupled with mass-spectrometry (2D-LCMS/MS) and bioinformatics analysis. A total of 273 proteins were identified, of which 133 (48.7%) were membrane proteins. We compared our data with membrane proteins of adult RBCs to identify common, and unique, surface membrane proteins. Twelve plasma membrane proteins with transmembrane domains and eight proteins with transmembrane domains but without known sub-cellular location were identified as unique-to-FNRBCs. Except for the transferrin receptor, all other 19 unique-to-FNRBC membrane proteins have never been described in RBCs. Reverse-transcriptase PCR (RT-PCR) and immunocytochemistry validated the 2D-LCMS/MS data. Our findings provide potential surface antigens for separation of primitive FNRBCs from maternal blood for noninvasive prenatal diagnosis, and to understand the biology of these rare cells.
KW - 2D-LC-MALDITOF/TOF-MS
KW - Erythrocytes
KW - Human fetal nucleated red blood cells
KW - Membrane protein profiling
KW - Noninvasive prenatal diagnosis
KW - RBC
UR - http://www.scopus.com/inward/record.url?scp=84866164341&partnerID=8YFLogxK
U2 - 10.1016/j.jprot.2012.07.020
DO - 10.1016/j.jprot.2012.07.020
M3 - Article
C2 - 22842289
AN - SCOPUS:84866164341
SN - 1874-3919
VL - 75
SP - 5762
EP - 5773
JO - Journal of Proteomics
JF - Journal of Proteomics
IS - 18
ER -