Intra-ramanome correlation analysis unveils metabolite conversion network from an isogenic population of cells

Abstract

To reveal the dynamic features of cellular systems, such as the correlation among phenotypes, a time or condition series set of samples is typically required. Here, we propose intra-ramanome correlation analysis (IRCA) to achieve this goal from just one snapshot of an isogenic population, via pairwise correlation among the cells of the thousands of Raman peaks in single-cell Raman spectra (SCRS), i.e., by taking advantage of the intrinsic metabolic heterogeneity among individual cells. For example, IRCA of Chlamydomonas reinhardtii under nitrogen depletion revealed metabolite conversions at each time point plus their temporal dynamics, such as protein-to-starch conversion fol-lowed by starch-to-triacylglycerol (TAG) conversion, and conversion of membrane lipids to TAG. Such among-cell correlations in SCRS vanished when the starch-biosyn-thesis pathway was knocked out yet were fully restored by genetic complementa-tion. Extension of IRCA to 64 microalgal, fungal, and bacterial ramanomes suggests the IRCA-derived metabolite conversion network as an intrinsic metabolic signature of isogenic cellular population that is reliable, species-resolved, and state-sensitive. The high-throughput, low cost, excellent scalability, and general extendibility of IRCA suggest its broad applications. IMPORTANCE Each isogenic population of cells is characterized by many phenotypes, which change with time and condition. Correlations among such phenotypes are fundamental to system function, yet revelation of such links typically requires multiple samples. Here, we showed that, by exploiting the intrinsic metabolic heterogeneity among individual cells, such interphenotype correlations can be unveiled via just one snapshot of an isogenic cellular population. Specifically, a network of potential metabolite conversions can be reconstructed using intra-ramanome correlation analysis (IRCA), by pairwise correlation of the thousands of Raman peaks or combination of peaks among single-cell Raman spectra sampled from just one instance of the cellular population. The ability to rapidly and noninvasively reveal intermetabolite conversions from just one snapshot of one sample should usher in many new opportu-nities in functional profiling of cellular systems.