Intrinsic Lipid Curvature and Bilayer Elasticity as Regulators of Channel Function: A Comparative Single-Molecule Study

被引:1
|
作者
Ashrafuzzaman, Mohammad [1 ,3 ]
Koeppe, Roger E. [2 ]
Andersen, Olaf S. [1 ]
机构
[1] Weill Cornell Med, Dept Physiol & Biophys, New York, NY 10065 USA
[2] Univ Arkansas, Dept Chem & Biochem, Fayetteville, AR 72701 USA
[3] King Saud Univ, Coll Sci, Dept Biochem, Riyadh 11451, Saudi Arabia
基金
美国国家卫生研究院;
关键词
lipid intrinsic curvature; elasticity; amphiphiles; bilayer-mediated regulation; gramicidin channel; alamethicin channel; MEMBRANE-PROTEIN FUNCTION; GRAMICIDIN-A; CONDUCTANCE HETEROGENEITY; ANTIMICROBIAL PEPTIDES; ALAMETHICIN CHANNELS; FREE-ENERGY; STATE; MODULATION; MECHANISM; PORE;
D O I
10.3390/ijms25052758
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Perturbations in bilayer material properties (thickness, lipid intrinsic curvature and elastic moduli) modulate the free energy difference between different membrane protein conformations, thereby leading to changes in the conformational preferences of bilayer-spanning proteins. To further explore the relative importance of curvature and elasticity in determining the changes in bilayer properties that underlie the modulation of channel function, we investigated how the micelle-forming amphiphiles Triton X-100, reduced Triton X-100 and the HII lipid phase promoter capsaicin modulate the function of alamethicin and gramicidin channels. Whether the amphiphile-induced changes in intrinsic curvature were negative or positive, amphiphile addition increased gramicidin channel appearance rates and lifetimes and stabilized the higher conductance states in alamethicin channels. When the intrinsic curvature was modulated by altering phospholipid head group interactions, however, maneuvers that promote a negative-going curvature stabilized the higher conductance states in alamethicin channels but destabilized gramicidin channels. Using gramicidin channels of different lengths to probe for changes in bilayer elasticity, we found that amphiphile adsorption increases bilayer elasticity, whereas altering head group interactions does not. We draw the following conclusions: first, confirming previous studies, both alamethicin and gramicidin channels are modulated by changes in lipid bilayer material properties, the changes occurring in parallel yet differing dependent on the property that is being changed; second, isolated, negative-going changes in curvature stabilize the higher current levels in alamethicin channels and destabilize gramicidin channels; third, increases in bilayer elasticity stabilize the higher current levels in alamethicin channels and stabilize gramicidin channels; and fourth, the energetic consequences of changes in elasticity tend to dominate over changes in curvature.
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页数:24
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