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Title: Membrane proteins of human fetal primitive nucleated red blood cells
Authors: Ponnusamy, S. 
Zhang, H.
Kadam, P.
Lin, Q. 
Lim, T.K. 
Sandhu, J.S.
Kothandaraman, N.
Mahyuddin, A.P.
Biswas, A.
Venkat, A.
Hew, C.-L. 
Joshi, S.B. 
Chung, M.C.M.
Choolani, M.
Human fetal nucleated red blood cells
Membrane protein profiling
Noninvasive prenatal diagnosis
Issue Date: 22-Oct-2012
Citation: Ponnusamy, S., Zhang, H., Kadam, P., Lin, Q., Lim, T.K., Sandhu, J.S., Kothandaraman, N., Mahyuddin, A.P., Biswas, A., Venkat, A., Hew, C.-L., Joshi, S.B., Chung, M.C.M., Choolani, M. (2012-10-22). Membrane proteins of human fetal primitive nucleated red blood cells. Journal of Proteomics 75 (18) : 5762-5773. ScholarBank@NUS Repository.
Abstract: 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. © 2012 Elsevier B.V.
Source Title: Journal of Proteomics
ISSN: 18743919
DOI: 10.1016/j.jprot.2012.07.020
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