Probing Asymmetric Charge Partitioning of Protein Oligomers during Tandem Mass Spectrometry.

ABSTRACT: Dissociation of gaseous protein complexes produced by native electrospray often induces an asymmetric partitioning of charge between ejected subunits. We present a simple asymmetric charge partitioning factor (ACPF) to quantify the magnitude of asymmetry in this effect. When applied to monomer ejection from the cytochrome c dimer and β-amylase tetramer, we found that the ~60-70% of precursor charge ending up in the ejected monomers corresponds to ACPFs of 1.38 and 2.51, respectively. Further, we used site-specific fragmentation from electron transfer dissociation (ETD) to identify differences in fragmentation and characterize domains of secondary-structure present in the dimer, ejected monomers, and monomers obtained directly from electrospray ionization (ESI). We found evidence of structu

SUBMITTER: Compton PD 

PROVIDER: S-EPMC4673687 | biostudies-literature | 2015 Nov

REPOSITORIES: biostudies-literature