Se mAb against the myc-epitope and a rabbit pAb against tubulin

Se mAb against the myc-epitope and a rabbit pAb against tubulin (Abcam), was performed on cells co-transfected with Yif1A siRNA and myc-Yif1A harvested from 60-mm dishes as described previously [31].Materials and Methods Cell culture and transfectionsHeLa cells stably expressing a GalNacT2-green fluorescent protein (GFP) [28] were maintained in minimal essential medium (Sigma-Aldrich, St. Louis, MO) containing 10 fetal bovine serum (Atlanta Biologicals, Norcross, GA) and 100 IU/ml penicillin and streptomycin (Mediatech, MedChemExpress MC-LR Herndon, VA) at 37uC in a 5 CO2 incubator. Transient plasmid DNA transfection of HeLa cells was performed with jetPEITM (Polyplus transfection, Illkirch, France), according to the manufacturer’s specifications using 0.5 mg DNA per 1 mL media. Transient co-transfection of HeLa cells with both plasmid DNA and siRNA was performed with jetPRIMETM (Polyplus transfection) according to the manufacturer’s specifications by using 150 ng of DNA and 10 pmol siRNA per 0.5 mL media. Transient siRNA transfections of siRNAs against Yif1A were performed using jetPRIMETM (Polyplus transfection) using 20 pmol siRNA per 0.5 mL media.Fluorescence microscopyAll images were obtained using a Yokagawa spinning disk confocal scanhead (Perkin Elmer Life and Analytical Sciences, Boston MA) mounted on an Axiovert 200 microscope (Carl Zeiss, Jena, Germany) with a 100X 1.4 numerical aperture (NA) objective (Carl Zeiss) and acquired using a 12-bit Orca ER digital camera (Hamamatsu Photonics, Hamamatsu City, Japan). Maximal value projections of sections at 0.3-mm spacing (5?/cell) were acquired using ImageJ (National Institutes of Health, Bethesda, MD).Quantification of efficiency of rescueFor each of our transgene replacement experiments, at least 100 cells were counted in three individual experiments and the data was calculated as the percentage of cells expressing the transgene that display ER whorls. In order to compare the different constructs over multiple sets of experiments, this percentage was normalized to the negative control for that experiment using the following formula: Efficiency = 1 ?(fraction cells expressing transgene with ER whorls/fraction cells expressing negative control with ER whorls). An efficiency of 1 reflects full rescue and 0 is a complete non-rescue.Results Both the cytoplasmic and transmembrane domains of Yip1A are required for ER structural maintenanceWe began by testing the cytoplasmic and transmembrane (TM) domains of Yip1A independently for their ability to regulate ER whorls. Two constructs based on the siRNA-immune HA-Yip1A parent rescue construct were generated (schematized in Fig. 1C). One replaced the entire C-terminal multi-pass TM domain of Yip1A with the single pass C-terminally anchored TM domain of Sec61b [32] so as to maintain ER membrane targeting of the cytoplasmic domain (HA-Yip1AN/Sec61bTM; schematized in Fig. 1F). The other truncated the entire N-terminal cytoplasmic domain (HA-Yip1A D1?18; schematized in Fig. 1I). Each construct was transiently transfected into HeLa cells together with the Yip1A siRNA and processed 72 hrs later for immunofluorescence using antibodies against the HA epitope and the integral ER membrane marker calnexin [33]. As expected, HA-Yip1A displayed primarily an ER exit site pattern at steady state (Fig. 1A) with some detectable 16960-16-0 price overlap with the ER marker calnexin (Fig. 1B). Similar to our previous report [10], few if any cells expressing wild type HA-Yip1A displayed whorls (F.Se mAb against the myc-epitope and a rabbit pAb against tubulin (Abcam), was performed on cells co-transfected with Yif1A siRNA and myc-Yif1A harvested from 60-mm dishes as described previously [31].Materials and Methods Cell culture and transfectionsHeLa cells stably expressing a GalNacT2-green fluorescent protein (GFP) [28] were maintained in minimal essential medium (Sigma-Aldrich, St. Louis, MO) containing 10 fetal bovine serum (Atlanta Biologicals, Norcross, GA) and 100 IU/ml penicillin and streptomycin (Mediatech, Herndon, VA) at 37uC in a 5 CO2 incubator. Transient plasmid DNA transfection of HeLa cells was performed with jetPEITM (Polyplus transfection, Illkirch, France), according to the manufacturer’s specifications using 0.5 mg DNA per 1 mL media. Transient co-transfection of HeLa cells with both plasmid DNA and siRNA was performed with jetPRIMETM (Polyplus transfection) according to the manufacturer’s specifications by using 150 ng of DNA and 10 pmol siRNA per 0.5 mL media. Transient siRNA transfections of siRNAs against Yif1A were performed using jetPRIMETM (Polyplus transfection) using 20 pmol siRNA per 0.5 mL media.Fluorescence microscopyAll images were obtained using a Yokagawa spinning disk confocal scanhead (Perkin Elmer Life and Analytical Sciences, Boston MA) mounted on an Axiovert 200 microscope (Carl Zeiss, Jena, Germany) with a 100X 1.4 numerical aperture (NA) objective (Carl Zeiss) and acquired using a 12-bit Orca ER digital camera (Hamamatsu Photonics, Hamamatsu City, Japan). Maximal value projections of sections at 0.3-mm spacing (5?/cell) were acquired using ImageJ (National Institutes of Health, Bethesda, MD).Quantification of efficiency of rescueFor each of our transgene replacement experiments, at least 100 cells were counted in three individual experiments and the data was calculated as the percentage of cells expressing the transgene that display ER whorls. In order to compare the different constructs over multiple sets of experiments, this percentage was normalized to the negative control for that experiment using the following formula: Efficiency = 1 ?(fraction cells expressing transgene with ER whorls/fraction cells expressing negative control with ER whorls). An efficiency of 1 reflects full rescue and 0 is a complete non-rescue.Results Both the cytoplasmic and transmembrane domains of Yip1A are required for ER structural maintenanceWe began by testing the cytoplasmic and transmembrane (TM) domains of Yip1A independently for their ability to regulate ER whorls. Two constructs based on the siRNA-immune HA-Yip1A parent rescue construct were generated (schematized in Fig. 1C). One replaced the entire C-terminal multi-pass TM domain of Yip1A with the single pass C-terminally anchored TM domain of Sec61b [32] so as to maintain ER membrane targeting of the cytoplasmic domain (HA-Yip1AN/Sec61bTM; schematized in Fig. 1F). The other truncated the entire N-terminal cytoplasmic domain (HA-Yip1A D1?18; schematized in Fig. 1I). Each construct was transiently transfected into HeLa cells together with the Yip1A siRNA and processed 72 hrs later for immunofluorescence using antibodies against the HA epitope and the integral ER membrane marker calnexin [33]. As expected, HA-Yip1A displayed primarily an ER exit site pattern at steady state (Fig. 1A) with some detectable overlap with the ER marker calnexin (Fig. 1B). Similar to our previous report [10], few if any cells expressing wild type HA-Yip1A displayed whorls (F.