TY - JOUR
T1 - Surfaceome mapping of primary human heart cells with CellSurfer uncovers cardiomyocyte surface protein LSMEM2 and proteome dynamics in failing hearts
AU - Berg Luecke, Linda
AU - Waas, Matthew
AU - Littrell, Jack
AU - Wojtkiewicz, Melinda
AU - Castro, Chase
AU - Burkovetskaya, Maria
AU - Schuette, Erin N.
AU - Buchberger, Amanda Rae
AU - Churko, Jared M.
AU - Chalise, Upendra
AU - Waknitz, Michelle
AU - Konfrst, Shelby
AU - Teuben, Roald
AU - Morrissette-McAlmon, Justin
AU - Mahr, Claudius
AU - Anderson, Daniel R.
AU - Boheler, Kenneth R.
AU - Gundry, Rebekah L.
N1 - Publisher Copyright:
© 2023, The Author(s).
PY - 2023/1
Y1 - 2023/1
N2 - Cardiac cell surface proteins are drug targets and useful biomarkers for discriminating among cellular phenotypes and disease states. Here we developed an analytical platform, CellSurfer, that enables quantitative cell surface proteome (surfaceome) profiling of cells present in limited quantities, and we apply it to isolated primary human heart cells. We report experimental evidence of surface localization and extracellular domains for 1,144 N-glycoproteins, including cell-type-restricted and region-restricted glycoproteins. We identified a surface protein specific for healthy cardiomyocytes, LSMEM2, and validated an anti-LSMEM2 monoclonal antibody for flow cytometry and imaging. Surfaceome comparisons among pluripotent stem cell derivatives and their primary counterparts highlighted important differences with direct implications for drug screening and disease modeling. Finally, 20% of cell surface proteins, including LSMEM2, were differentially abundant between failing and non-failing cardiomyocytes. These results represent a rich resource to advance development of cell type and organ-specific targets for drug delivery, disease modeling, immunophenotyping and in vivo imaging.
AB - Cardiac cell surface proteins are drug targets and useful biomarkers for discriminating among cellular phenotypes and disease states. Here we developed an analytical platform, CellSurfer, that enables quantitative cell surface proteome (surfaceome) profiling of cells present in limited quantities, and we apply it to isolated primary human heart cells. We report experimental evidence of surface localization and extracellular domains for 1,144 N-glycoproteins, including cell-type-restricted and region-restricted glycoproteins. We identified a surface protein specific for healthy cardiomyocytes, LSMEM2, and validated an anti-LSMEM2 monoclonal antibody for flow cytometry and imaging. Surfaceome comparisons among pluripotent stem cell derivatives and their primary counterparts highlighted important differences with direct implications for drug screening and disease modeling. Finally, 20% of cell surface proteins, including LSMEM2, were differentially abundant between failing and non-failing cardiomyocytes. These results represent a rich resource to advance development of cell type and organ-specific targets for drug delivery, disease modeling, immunophenotyping and in vivo imaging.
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U2 - 10.1038/s44161-022-00200-y
DO - 10.1038/s44161-022-00200-y
M3 - Article
C2 - 36950336
AN - SCOPUS:85162110173
SN - 2731-0590
VL - 2
SP - 76
EP - 95
JO - Nature Cardiovascular Research
JF - Nature Cardiovascular Research
IS - 1
ER -