The nanoscale organization of reticulon 4 shapes local endoplasmic reticulum structure in situ

Fuentes and Marin et al. show that Rtn4 forms linear-shaped oligomers containing an average of five Rtn4 proteins that localize to the sides of elliptical tubules with orientations parallel to the tubule axis. These oligomers increase local curvature in the ER membrane by increasing local Rtn4 density. The endoplasmic reticulum's (ER's) structure is directly linked to the many functions of the ER, but its formation is not fully understood. We investigate how the ER-membrane curving protein reticulon 4 (Rtn4) localizes to and organizes in the membrane and how that affects the local ER structure. We show a strong correlation between the local Rtn4 density and the local ER membrane curvature. Our data further reveal that the typical ER tubule possesses an elliptical cross-section with Rtn4 enriched at either end of the major axis. Rtn4 oligomers are linear shaped, contain about five copies of the protein, and preferentially orient parallel to the tubule axis. Our observations support a mechanism in which oligomerization leads to an increase of the local Rtn4 concentration with each molecule, increasing membrane curvature through a hairpin wedging mechanism. This quantitative analysis of Rtn4 and its effects on the ER membrane result in a new model of tubule shape as it relates to Rtn4.