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. 2011 Aug 15;6(8):e23350. doi: 10.1371/journal.pone.0023350

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Zong 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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A. GFP -GAP273, -TRAPPC9, -TRAPPC9(L772Δ) and -TRAPPC9(R475X) were tested for the interaction with Myc-tagged TRAPPC2. The levels of protein expression in the transfected lysates are shown in lanes 1 to 4. Lanes 5 to 8 are immunoprecipitants. Full-length TRAPPC9 was efficiently pulled down by Myc-TRAPPC2 (lane 6), but not the deletion mutants of TRAPPC9 (lane 7 and 8), or negative control GFP-GAP273 (lane 5). B. Full-length and deletional mutants of TRAPPC9 were tested for the interaction with Myc-tagged TRAPPC10. The levels of protein expression in the transfected lysates are shown in lanes 1 to 4. Lanes 5 to 8 are immunoprecipitants. Full-length TRAPPC9 was efficiently pulled down by Myc-TRAPPC10 (lane 6), but not the deletional mutants (lane 7 and 8), or negative control GFP-GAP273 (lane 5). The experiments shown are representatives of two independent experiments.