4.4 Review

The multiple assemblies of VDAC: from conformational heterogeneity to β-aggregation and amyloid formation

Journal

BIOCHEMICAL SOCIETY TRANSACTIONS
Volume 44, Issue -, Pages 1531-1540

Publisher

PORTLAND PRESS LTD
DOI: 10.1042/BST20160114

Keywords

-

Ask authors/readers for more resources

From their cellular localisation, to their atomic structure and their involvement in mitochondrial- driven cell death, voltage-dependent anion channels (VDACs) have challenged the scientific community with enigmas and paradoxes for over four decades. VDACs form active monomer channels in lipid bilayers, but they can also organise in multimeric assemblies. What induces, regulates and/or controls the monomer-multimer dynamics at the cellular level is not known. However, these state transitions appear to be relevant for mitochondria in making life or death decisions and for driving developmental processes. This review starts with a general introduction on VDACs and continues by examining VDAC oligomerisation/aggregation in light of recent discussions on VDAC-beta-amyloid interactions and their involvement in Alzheimer's disease.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available