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. 2015 Sep 25;10(9):e0138508. doi: 10.1371/journal.pone.0138508

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© 2015 Zulliger et al

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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Fig 1 — Euler diagrams depicting results from LC-MS studies to identify RDS/ROM-1 interacting partners. Numbers in each diagram represent proteins identified. A-B. WT and rds ^-/- retinal extracts were IPed using RDS mAB 2E7 (A) or ROM1 mAB 2H5 (B), cross-linked to sepharose followed by LC-MS. C. This diagram depicts overlap between proteins identified in RDS pull-down (A) and ROM-1 pull down (B) after subtraction of negative controls (blue circles A-B). D. WT retinal extracts were IPed with anti-Syn3B-SySy or IgG coupled to protein A beads followed by LC-MS. E-F. These diagrams depict overlap between proteins in the RDS (E-left) or ROM-1 (E-right) IP and the Syn3B IP, or overlap between all three (F).