Jun 29, 2017
Volume 170Issue 1p1-214
Open Archive
On the cover: Proteins, pathogens, and other cargos enter the cell by a process called
endocytosis. The last step of this process, scission, involves cutting the membrane
enveloping the cargo to release it into the cell. In this issue, Simunovic and coworkers
(pp. 172–184) describe a new scission mechanism that does not rely on the canonical
scission module dynamin; instead, an elongating tubular membrane breaks due to friction.
After the cargo invaginates the membrane forming a tube, BAR domain proteins (green
crescent particles) form a scaffold around the tube. The motor protein dynenin (depicted
here as the super heroine) grabs and elongates the tube while walking on microtubules.
The friction between the tightly bound BAR protein scaffold and the lipids underneath
and the consequent extensile force increases the tension in the tube and causes it
to break, allowing the cargo to enter the trafficking pathways in the cell. Cover
illustrated by Maja Ðeke....Show more
On the cover: Proteins, pathogens, and other cargos enter the cell by a process called
endocytosis. The last step of this process, scission, involves cutting the membrane
enveloping the cargo to release it into the cell. In this issue, Simunovic and coworkers
(pp. 172–184) describe a new scission mechanism that does not rely on the canonical
scission module dynamin; instead, an elongating tubular membrane breaks due to friction.
After the cargo invaginates the membrane forming a tube, BAR domain proteins (green
crescent particles) form a scaffold around the tube. The motor protein dynenin (depicted
here as the super heroine) grabs and elongates the tube while walking on microtubules.
The friction between the tightly bound BAR protein scaffold and the lipids underneath
and the consequent extensile force increases the tension in the tube and causes it
to break, allowing the cargo to enter the trafficking pathways in the cell. Cover
illustrated by Maja Ðeke.