Biological Function Assignment Across Taxonomic Levels in Mass-Spectrometry-Based Metaproteomics via a Modified Expectation Maximization Algorithm
A major challenge in mass-spectrometry-based metaproteomics is accurately identifying and quantifying biological functions across the full taxonomic lineage of microorganisms. This issue stems from what we refer to as the "shared confidently identified peptide problem". To address this issue, most metaproteomics tools rely on the lowest common ancestor (LCA) algorithm to assign biological functions, which often leads to incomplete biological function assignments across the full taxonomic lineage of identified microorganisms. To overcome this limitation, we implemented an expectation-maximization (EM) algorithm, along with a biological function database, within MiCId workflow. Using synthetic datasets, our study demonstrates that the enhanced MiCId workflow achieves better control over false discoveries and improved accuracy in microorganism identification and biomass estimation compared to Unipept and MetaGOmics. Additionally, the updated MiCId offers improved accuracy and better control of false discoveries in biological function identification compared to Unipept, along with reliable computation of function abundances across the full taxonomic lineage of identified microorganisms. Reanalyzing human oral and gut microbiome datasets using the enhanced MiCId workflow, we show that the results are consistent with those reported in the original publications, which were analyzed using the Galaxy-P platform with MEGAN5 and the MetaPro-IQ approach with Unipept, respectively.