<p>(A) M71::GFP mutations F12D;I13H;L14D;G15V;G16T (FILGG to DHDGG), Y35A, P58V;M59T;Y60N (PMY to VTN), M98E, C169A, Y176T;F177C (FY to TC), C178A and Y217A. None of these mutations gave raise to any GFP-labeled filopodia. (B) M71::GFP mutations with N-linked glycosylation modifications: 4x NQS, 4x NSS, NQS to NGT, NQS to NAT, Nt to K4 Nt. (C) Addition of leader sequences (Kirrel2, 5HT3, Calcumenin, Rhodopsin, Endothelin, LUCY and LUCY-FLAG) to M71::GFP did not relocate GFP expression into the filopodia. (A-C) Co-expression with RTP1S for all M71::GFP mutations did not increase the presence of any GFP-labeled filopodia.</p
(A) Depiction of Dfm1, which highlights L1, TM2, TM6, and its SHP box domain. The table indicates th...
<p>(A) The Apm1-deletion (Δ<i>apm1</i>), <i>chc1-1</i> mutant and <i>ypt3-i5</i> mutant expressing c...
Background: The green fluorescent protein (GFP) of Aequorea victoria is emerging as a unique tool fo...
<p>(A) M71::GFP chimeras with Nt-mβ2AR, Ct-mβ2AR, Nt-and Ct- mβ2AR. None of these chimeras led to GF...
<p>(A) M71::GFP expression in OP6 cells in trapped perinuclearly (A’) Same cell with colabelling of ...
<p>(A) Cytosolic GFP shows diffuse fluorescence in the cytoplasm of an OP6 cell and does not co-loca...
<p>(A) <i>FgRAB51</i>, <i>FgRAB7</i> and <i>FgRAB8</i> deletion mutants expressing the GFP-FgAtg9 fu...
<p>Ability of GFP-tagged stomatin mutants to target the plasma membrane, form oligomers, and/or asso...
<p><b>A)</b> L6 myoblasts transiently transfected with FLAG-GLUT1 or FLAG-GLUT1 with S490A or S490D ...
(A and B) Semisolid surface penetration by WT E. faecalis MMH594 or the Mariner transposon mutants g...
<p>Cell surface expression and fusion assay results with B cells with gH mutants in the R488, S507 a...
<p>(A) Nonphosphorylated LCRMP-1 (T628A) mutant impairs filopodia formation. CL1-0 cells were transi...
<p>HeLa cells were transiently co-transfected with the C-terminally HA-tagged Endoglin pCMV5 plasmid...
<p>(A and B) The replacement of either the Ct or the Nt of mβ2AR with the one of M71 does not block ...
<p>A) Treatment with 100 ng/ml EGF for 2 h induces pronounced formation of filopodia. Cells were sta...
(A) Depiction of Dfm1, which highlights L1, TM2, TM6, and its SHP box domain. The table indicates th...
<p>(A) The Apm1-deletion (Δ<i>apm1</i>), <i>chc1-1</i> mutant and <i>ypt3-i5</i> mutant expressing c...
Background: The green fluorescent protein (GFP) of Aequorea victoria is emerging as a unique tool fo...
<p>(A) M71::GFP chimeras with Nt-mβ2AR, Ct-mβ2AR, Nt-and Ct- mβ2AR. None of these chimeras led to GF...
<p>(A) M71::GFP expression in OP6 cells in trapped perinuclearly (A’) Same cell with colabelling of ...
<p>(A) Cytosolic GFP shows diffuse fluorescence in the cytoplasm of an OP6 cell and does not co-loca...
<p>(A) <i>FgRAB51</i>, <i>FgRAB7</i> and <i>FgRAB8</i> deletion mutants expressing the GFP-FgAtg9 fu...
<p>Ability of GFP-tagged stomatin mutants to target the plasma membrane, form oligomers, and/or asso...
<p><b>A)</b> L6 myoblasts transiently transfected with FLAG-GLUT1 or FLAG-GLUT1 with S490A or S490D ...
(A and B) Semisolid surface penetration by WT E. faecalis MMH594 or the Mariner transposon mutants g...
<p>Cell surface expression and fusion assay results with B cells with gH mutants in the R488, S507 a...
<p>(A) Nonphosphorylated LCRMP-1 (T628A) mutant impairs filopodia formation. CL1-0 cells were transi...
<p>HeLa cells were transiently co-transfected with the C-terminally HA-tagged Endoglin pCMV5 plasmid...
<p>(A and B) The replacement of either the Ct or the Nt of mβ2AR with the one of M71 does not block ...
<p>A) Treatment with 100 ng/ml EGF for 2 h induces pronounced formation of filopodia. Cells were sta...
(A) Depiction of Dfm1, which highlights L1, TM2, TM6, and its SHP box domain. The table indicates th...
<p>(A) The Apm1-deletion (Δ<i>apm1</i>), <i>chc1-1</i> mutant and <i>ypt3-i5</i> mutant expressing c...
Background: The green fluorescent protein (GFP) of Aequorea victoria is emerging as a unique tool fo...