Proteomics

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SAPrIm 2.0: A semi-automated protocol for mid-throughput soluble HLA immunopeptidomics


ABSTRACT: Human leukocyte antigen (HLA) molecules are pivotal in guiding human adaptive immune responses through their presentation of peptide ligands, collectively known as the immunopeptidome. This process is central to the development of cancer immunotherapies, such as vaccines and T-cell therapies. Profiling the immunopeptidome from plasma and other biofluids has gained increasing traction, as it offers a minimally invasive approach for monitoring disease states and immune responses toward cancer therapy. Here we present the second iteration of SAPrIm, a refined immunopeptidomics tool optimized for soluble HLA analysis. It can process up to 12 samples per batch within a day. This workflow is positioned to advance the field of immunopeptidomics by enabling efficient plasma-based comparative analyses and mid-size cohort studies.

INSTRUMENT(S):

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Blood Plasma

SUBMITTER: ERWIN TANUWIDJAYA  

LAB HEAD: Pouya Faridi

PROVIDER: PXD058880 | Pride | 2025-05-26

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
BLANK001.raw Raw
BLANK001.raw.mgf Mgf
BLANK_DIA.raw Raw
DDA_5000_Fx1.raw Raw
DDA_5000_Fx1.raw.mgf Mgf
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Publications

SAPrIm 2.0: a semi-automated protocol for mid-throughput soluble HLA immunopeptidomics.

Tanuwidjaya Erwin E   Lim Kam Sian Terry C C TCC   Steele Joel R JR   Goncalves Gabriel G   Woodhouse Isaac B IB   Chang Janet J   Ooi Joshua D JD   Schittenhelm Ralf B RB   Faridi Pouya P  

Frontiers in immunology 20250424


Human leukocyte antigen (HLA) molecules are pivotal in guiding human adaptive immune responses through their presentation of peptide ligands, collectively known as the immunopeptidome. This process is central to the development of cancer immunotherapies, such as vaccines and T-cell therapies. Profiling the immunopeptidome from plasma and other biofluids has gained increasing traction, as it offers a minimally invasive approach for monitoring disease states and immune responses toward cancer ther  ...[more]

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