Accelerating SNARE‐Mediated Membrane Fusion by DNA–Lipid Tethers. Issue 48 (6th October 2015)

• Record Type: Journal Article
• Authors: Xu, Weiming; Wang, Jing; Rothman, James E.; Pincet, Frédéric
• Is Part Of: Angewandte Chemie international edition. Volume 54:Issue 48(2015)
• Page Start: 14388
• Page End: 14392
• Publication Date: 2015-10-06
• Subjects: liposomes -- membrane fusion -- membrane proteins -- protein mimics -- ssDNA–lipid conjugation; Chemistry -- Periodicals; 540
• DOI: 10.1002/anie.201506844
• Languages: English
• ISSNs: 1433-7851

Abstract

Abstract: SNARE proteins are the core machinery to drive fusion of a vesicle with its target membrane. Inspired by the tethering proteins that bridge the membranes and thus prepare SNAREs for docking and fusion, we developed a lipid‐conjugated ssDNA mimic that is capable of regulating SNARE function, in situ. The DNA–lipid tethers consist of a 21 base pairs binding segment at the membrane distal end that can bridge two liposomes via specific base‐pair hybridization. A linker at the membrane proximal end is used to control the separation distance between the liposomes. In the presence of these artificial tethers, SNARE‐mediated lipid mixing is significantly accelerated, and the maximum fusion rate is obtained with the linker shorter than 40 nucleotides. As a programmable tool orthogonal to any native proteins, the DNA–lipid tethers can be further applied to regulate other biological processes where capturing and bridging of two membranes are the prerequisites for the subsequent protein function. Abstract : A non‐fusogenic DNA–lipid mimic of tethering factors was developed that significantly stimulates SNARE‐mediated lipid mixing. Using linkers with various lengths, two bridged membranes are kept within a controlled distance (see picture; SUV=small unilamellar vesicle). The DNA–lipid tethers can be applied to regulate other biological processes where capturing and bridging of two membranes are the prerequisites for protein function.