Intrinsic Lipid Curvature and Bilayer Elasticity as Regulators of Channel Function: A Comparative Single-Molecule Study
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作者:
Ashrafuzzaman, Mohammad
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Weill Cornell Med, Dept Physiol & Biophys, New York, NY 10065 USA
King Saud Univ, Coll Sci, Dept Biochem, Riyadh 11451, Saudi ArabiaWeill Cornell Med, Dept Physiol & Biophys, New York, NY 10065 USA
Ashrafuzzaman, Mohammad
[1
,3
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Koeppe, Roger E.
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Univ Arkansas, Dept Chem & Biochem, Fayetteville, AR 72701 USAWeill Cornell Med, Dept Physiol & Biophys, New York, NY 10065 USA
Koeppe, Roger E.
[2
]
Andersen, Olaf S.
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Weill Cornell Med, Dept Physiol & Biophys, New York, NY 10065 USAWeill Cornell Med, Dept Physiol & Biophys, New York, NY 10065 USA
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
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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Univ Chinese Acad Sci, Wenzhou Inst, Wenzhou 325001, Peoples R China
Wenzhou Kean Univ, Wenzhou 325060, Peoples R ChinaUniv Chinese Acad Sci, Wenzhou Inst, Wenzhou 325001, Peoples R China
Zhang, Yiming
Ji, Zongzhou
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Univ Chinese Acad Sci, Wenzhou Inst, Wenzhou 325001, Peoples R China
Northeastern Univ, Shenyang 110819, Peoples R ChinaUniv Chinese Acad Sci, Wenzhou Inst, Wenzhou 325001, Peoples R China
Ji, Zongzhou
Wang, Xin
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Univ Chinese Acad Sci, Wenzhou Inst, Wenzhou 325001, Peoples R ChinaUniv Chinese Acad Sci, Wenzhou Inst, Wenzhou 325001, Peoples R China
Wang, Xin
Cao, Yi
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Univ Chinese Acad Sci, Wenzhou Inst, Wenzhou 325001, Peoples R China
Jinan Microecol Biomed Shandong Lab, Shounuo City Light West Block,Qingdao Rd 3716, Jinan 250117, Peoples R China
Nanjing Univ, Dept Phys, Natl Lab Solid State Microstruct, Nanjing 210093, Peoples R ChinaUniv Chinese Acad Sci, Wenzhou Inst, Wenzhou 325001, Peoples R China
Cao, Yi
Pan, Hai
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Univ Chinese Acad Sci, Wenzhou Inst, Wenzhou 325001, Peoples R ChinaUniv Chinese Acad Sci, Wenzhou Inst, Wenzhou 325001, Peoples R China
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Tokyo Inst Technol, Dept Phys, Tokyo 1528551, JapanTokyo Inst Technol, Dept Phys, Tokyo 1528551, Japan
Uchiyama, Daisuke
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Oikawa, Hiroyuki
Otomo, Kohei
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Tokyo Inst Technol, Dept Phys, Tokyo 1528551, JapanTokyo Inst Technol, Dept Phys, Tokyo 1528551, Japan
Otomo, Kohei
Nango, Mamoru
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Osaka City Univ, OCU Adv Res Inst Nat Sci & Technol, Osaka 5588585, Japan
Nagoya Inst Technol, Grad Sch Engn, Dept Frontier Mat, Nagoya, Aichi 4668555, JapanTokyo Inst Technol, Dept Phys, Tokyo 1528551, Japan
Nango, Mamoru
Dewa, Takehisa
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Nagoya Inst Technol, Grad Sch Engn, Dept Frontier Mat, Nagoya, Aichi 4668555, JapanTokyo Inst Technol, Dept Phys, Tokyo 1528551, Japan
Dewa, Takehisa
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Fujiyoshi, Satoru
Matsushita, Michio
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Tokyo Inst Technol, Dept Phys, Tokyo 1528551, JapanTokyo Inst Technol, Dept Phys, Tokyo 1528551, Japan