4.7 Article

Simple Method To Characterize the Ciliary Proteome of Multiciliated Cells

Journal

JOURNAL OF PROTEOME RESEARCH
Volume 19, Issue 1, Pages 391-400

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jproteome.9b00589

Keywords

cilia; multiciliated cells; Xenopus laevis; DTBP

Funding

  1. National Research Foundation of Korea - Ministry of Science, ICT and Future Planning [NRF-2016R1C1B2009302, 2015R1D1A1A02061763, 2018R1A2B2007545]
  2. Ministry of Education [2018R1A6A1A03025810]
  3. Institute for Basic Science [IBS-R022-D1]
  4. UNIST research fund [1.180063, 1.180040]
  5. Science Research Center program of the National Research Foundation (NRF) - Ministry of Science, ICT and Future Planning [2015R1A5A1009024]
  6. National Xenopus Resource Center [RRID:SCR_013731]
  7. Xenbase [RRID:SCR_ 003280]
  8. National Research Foundation of Korea [2018R1A2B2007545, 2015R1D1A1A02061763] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Motile cilia of multiciliated epithelial cells have important roles in animal development and cell homeostasis. Although several studies have identified and reported proteins localized in this complex organelle and the related immotile primary cilia from various cell types, it is still challenging to isolate high quantities of ciliary proteins for proteomic analysis. In this study, African clawed frog (Xenopus laevis) embryos, which have many multiciliated cells in the epidermis, were treated with a simple ionic buffer to identify 1009 proteins conserved across vertebrates; these proteins were putatively localized in motile cilia. Using two ciliary proteome databases, we confirmed that previously validated cilia-associated proteins are highly enriched in our ciliary proteome. Proteins localized at the transition zone and Ellis-van Creveld zone, which are distinct regions at the base of cilia, near the junction with the apical cell surface, were isolated using our method. Among the newly identified ciliary proteins, we report that KRT17 may have an unrecognized function in motile cilia. Hence, the method developed in this study would be useful for understanding the ciliary proteome.

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