Hydrophobic mismatch modulates stability and plasticity of human mitochondrial VDAC2

April 8, 2019

Title

Hydrophobic mismatch modulates stability and plasticity of human mitochondrial VDAC2

Author

Shashank Ranjan Srivastava, Punit Zadafiya, Radhakrishan Mahalakshmi

Year

2018

Journal

Biophysical Journal

Abstract

The human mitochondrial outer membrane protein VDAC2 (voltage-dependent anion channel) is a β-barrel metabolite flux channel that is indispensable for cell survival. It is well established that physical forces imposed on a transmembrane protein by its surrounding lipid environment decides protein structure and stability. Yet, how the mitochondrial membrane and protein-lipid interplay together regulate hVDAC2 stability is unknown. Here, we combine experimental biophysical investigations of protein stability with all-atom molecular dynamics simulations to study the effect of the most abundant mitochondrial phosphocholine (PC) lipids on hVDAC2. We demonstrate experimentally that increasing the PC lipid acyl chain length from diC14:0–diC18:0-PC has a non-linear effect on the β-barrel. We show that protein stability is highest in diC16:0-PC that exhibits a negative mismatch with the hVDAC2 barrel. Our simulations also reveal that structural rigidity of hVDAC2 is highest under optimal negative mismatch provided by diC16:0-PC bilayers. Further, we validate our observations by altering the physical properties of PC membranes indirectly using cholesterol. We propose that VDAC plasticity and stability in the mitochondrial outer membrane are modulated by physical properties of the bilayer.

Instrument

J-815

Keywords

Circular dichroism, Secondary structure, Thermal stability, Protein folding, Kinetics, Aggregation, Thermodynamics, Membrane interactions, Biochemistry