Highlights d NTPDase3 is a marker highly expressed in adult human pancreatic b cells d NTPDase3 expression is maintained in b cells from individuals with diabetes d Use of an NTPDase3 antibody enables isolation of live b cells from human islets d NTPDase3 antibody also allows detection of human b cells by in vivo imaging
Cytochrome
c
(cyt
c
) can undergo reversible conformational changes under biologically relevant conditions. Revealing these alternative cyt
c
conformers at the cell and tissue level is challenging. A monoclonal antibody (mAb) identifying a key conformational change in cyt
c
was previously reported, but the hybridoma was rendered nonviable. To resurrect the mAb in a recombinant form, the amino-acid sequences of the heavy and light chains were determined by peptide mapping–mass spectrometry–bioinformatic analysis and used to construct plasmids encoding the full-length chains. The recombinant mAb (R1D3) was shown to perform similarly to the original mAb in antigen-binding assays. The mAb bound to a variety of oxidatively modified cyt
c
species (e.g., nitrated at Tyr74 or oxidized at Met80), which lose the sixth heme ligation (Fe-Met80); it did not bind to several cyt
c
phospho- and acetyl-mimetics. Peptide competition assays together with molecular dynamic studies support that R1D3 binds a neoepitope within the loop 40–57. R1D3 was employed to identify alternative conformations of cyt
c
in cells under oxidant- or senescence-induced challenge as confirmed by immunocytochemistry and immunoaffinity studies. Alternative conformers translocated to the nuclei without causing apoptosis, an observation that was further confirmed after pinocytic loading of oxidatively modified cyt
c
to B16-F1 cells. Thus, alternative cyt
c
conformers, known to gain peroxidatic function, may represent redox messengers at the cell nuclei. The availability and properties of R1D3 open avenues of interrogation regarding the presence and biological functions of alternative conformations of cyt
c
in mammalian cells and tissues.
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