HPLC chromatogram peaks that were selected for further proteomics analysis
HPLC chromatogram peaks that were selected for further proteomics analysis. stoichiometry and a high affinity of UKN2b_2.8 E2e for mAb CBH4D.(1.23 MB TIF) ppat.1000762.s003.tif (1.1M) GUID:?1CE6AB14-4ECE-4281-A8B8-008CB5E7D32F Figure S2: Alignment of HCV E2 amino acid sequences from strains H77, JFH-1 and UKN2b_2.8. Given the deamination of Asn residues by PNGase F, they are turned into Asp residues. Predicted trypsin cleavage sites (grey triangles) and N-glycosylation sites (empty diamonds) are indicated, cysteines are boxed and the respective disulfide bridges displayed (-SS-). Peptides identified after tryptic cleavage are shaded, named according to the respective isolate and numbered sequentially following the amino acid sequence of E2.(2.52 MB TIF) ppat.1000762.s004.tif (2.3M) GUID:?1D97BB29-532B-40D3-813E-15C6266C0AF0 Figure S3: Proteomics results for the determination of the disulfide bridges. HPLC chromatogram peaks that were selected for further proteomics analysis. Results of…