Abstract

Sub-cellular localisation of proteins is an essential post-translational regulatory mechanism that can be assayed using high-throughput mass spectrometry (MS). These MS-based spatial proteomics experiments enable us to pinpoint the sub-cellular distribution of thousands of proteins in a specific system under controlled conditions. Recent advances in high-throughput MS methods have yielded a plethora of experimental spatial proteomics data for the cell biology community. Yet, there are many third-party data sources, such as immunofluorescence microscopy or protein annotations and sequences, which represent a rich and vast source of complementary information. We present a unique transfer learning classification framework that utilises a nearest-neighbour or support vector machine system, to integrate heterogeneous data sources to considerably improve on the quantity and quality of sub-cellular protein assignment. We demonstrate the utility of our algorithms through evaluation of five experimental datasets, from four different species in conjunction with four different auxiliary data sources to classify proteins to tens of sub-cellular compartments with high generalisation accuracy. We further apply the method to an experiment on pluripotent mouse embryonic stem cells to classify a set of previously unknown proteins, and validate our findings against a recent high resolution map of the mouse stem cell proteome. The methodology is distributed as part of the open-source Bioconductor pRoloc suite for spatial proteomics data analysis.

Highlights

  • Cell biology is currently undergoing a data-driven paradigm shift [1]

  • Sub-cellular localisation of proteins is critical to their function in all cellular processes; proteins localising to their intended micro-environment, e.g organelles, vesicles or macromolecular complexes, will meet the interaction partners and biochemical conditions

  • We have adapted a classic application of inductive transfer learning (TL) [6] using experimental quantitative proteomics data as the primary source and Gene Ontology Cellular Compartment (GO cellular component (CC)) terms as the auxiliary source

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Summary

Introduction

Cell biology is currently undergoing a data-driven paradigm shift [1]. Molecular biology tools, imaging, biochemical analyses and omics technologies, enable cell biologists to track the complexity of many fundamental processes such as signal transduction, gene regulation, protein interactions and sub-cellular localisation [2]. This remarkable success, has resulted in dramatic growth in data over the last decade, both in terms of size and heterogeneity. Coupled with this influx of experimental data, databases such as UniProt [3] and the Gene Ontology [4] have become more information rich, providing valuable resources for the community. One of the biggest challenges in computational biology is how to meaningfully integrate heterogeneous data; transfer learning, a paradigm in machine learning, is ideally suited to this task

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