New PhytologistMolecular BiologyPeer-reviewed journal article
Proteomic analysis of the pyrenoid-traversing membranes of Chlamydomonas reinhardtii reveals novel components
Eric FrankliniD, Lianyong WangiD, Edward R. CruziD, Keenan DuggaliD, Sabrina L. ErguniD, Aastha GardeiD, Alice LunardoniD, Weronika PatenaiD, Cole PaciniiD, Martin C. JonikasiD
Abstract
O_LIPyrenoids are algal CO2-fixing organelles that mediate approximately one-third of global carbon fixation. Most pyrenoids are traversed by membranes that are thought to supply them with concentrated CO2. Despite the critical nature of these membranes for pyrenoid function, they are poorly understood, with few protein components known in any species. C_LIO_LIHere, we identify protein components of the pyrenoid-traversing membranes from the leading model alga, Chlamydomonas reinhardtii, by affinity purification and mass spectrometry of membrane fragments. Our proteome includes previously-known proteins as well as novel candidates. C_LIO_LIWe further characterize two of the novel pyrenoid-traversing membrane-resident proteins: Cre10.g452250, which we name Pyrenoid Membrane Enriched 1 (PME1), and Cre02.g143550, also known as Low-CO2-Induced 16 (LCI16). We confirm the pyrenoid-traversing membrane localization of LCI16 and observe that PME1 and LCI16 physically interact. We find that neither protein is required for normal membrane morphology or growth under CO2-limiting conditions, but that both mutants show a similar proteomic profile to those of established pyrenoid mutants. C_LIO_LITaken together, our study identifies the proteome of the pyrenoid-traversing membranes and initiates the characterization of a novel pyrenoid-traversing membrane complex, building toward a mechanistic understanding of the pyrenoid. C_LI
- organism: C. elegans
- assay: proteomics
- research focus: protein structure prediction
- approach: experimental assay
- Citations
- 10
- FWCI
- 3.01
- Field percentile
- top 7%
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