Exploring fast proton transfer events associated with lateral proton diffusion on the surface of membranes

被引:52
作者
Amdursky, Nadav [1 ]
Lin, Yiyang [2 ]
Aho, Noora [3 ,4 ]
Groenhof, Gerrit [3 ,4 ]
机构
[1] Technion Israel Inst Technol, Schulich Fac Chem, IL-3200003 Haifa, Israel
[2] Imperial Coll London, Dept Mat, London SW7 2AZ, England
[3] Univ Jyvaskyla, Dept Chem, FIN-40014 Jyvaskyla, Finland
[4] Univ Jyvaskyla, NanoSci Ctr, FIN-40014 Jyvaskyla, Finland
基金
芬兰科学院;
关键词
proton diffusion; excited-state proton transfer; lipid vesicles; photoacid; molecular dynamics; GEMINATE RECOMBINATION; WATER; PHOTOACIDS; ENERGY; BULK; INTERFACE; MECHANISM; DYNAMICS; EXCHANGE;
D O I
10.1073/pnas.1812351116
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Proton diffusion (PD) across biological membranes is a fundamental process in many biological systems, and much experimental and theoretical effort has been employed for deciphering it. Here, we report on a spectroscopic probe, which can be tightly tethered to the membrane, for following fast (nanosecond) proton transfer events on the surface of membranes. Our probe is composed of a photoacid that serves as our light-induced proton source for the initiation of the PD process. We use our probe to followPD, and its pH dependence, on the surface of lipid vesicles composed of a zwitterionic headgroup, a negative headgroup, a headgroup that is composed only from the negative phosphate group, or a positive headgroup without the phosphate group. We reveal that the PD kinetic parameters are highly sensitive to the nature of the lipid headgroup, ranging from a fast lateral diffusion at some membranes to the escape of protons from surface to bulk (and vice versa) at others. By referring to existing theoretical models for membrane PD, we found that while some of our results confirm the quasi-equilibrium model, other results are in line with the nonequilibrium model.
引用
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页码:2443 / 2451
页数:9
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