Proteomics

Dataset Information

0

MSP-MS of PC1 and PC2 pH 5.5 at 37C


ABSTRACT: MSP-MS of PC1 and PC2 pH 5.5 at 37C. Part of Neuropeptide processing study

INSTRUMENT(S): Q Exactive

ORGANISM(S): Synthetic Construct (ncbitaxon:32630)

SUBMITTER: Vivian Hook   Anthony ODonoghue  

PROVIDER: MSV000088092 | MassIVE |

SECONDARY ACCESSION(S): PXD028455

REPOSITORIES: MassIVE

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Publications

Distinct Dibasic Cleavage Specificities of Neuropeptide-Producing Cathepsin L and Cathepsin V Cysteine Proteases Compared to PC1/3 and PC2 Serine Proteases.

Yoon Michael C MC   Ames Janneca J   Mosier Charles C   Jiang Zhenze Z   Podvin Sonia S   O'Donoghue Anthony J AJ   Hook Vivian V  

ACS chemical neuroscience 20220105 2


Neuropeptides, functioning as peptide neurotransmitters and hormones, are generated from proneuropeptide precursors by proteolytic processing at dibasic residue sites (i.e., KR, RK, KK, RR). The cysteine proteases cathepsin L and cathepsin V, combined with the serine proteases proprotein convertases 1 and 2 (PC1/3 and PC2), participate in proneuropeptide processing to generate active neuropeptides. To compare the dibasic cleavage properties of these proteases, this study conducted global, unbias  ...[more]

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