» Articles » PMID: 27216038

Protons at the Speed of Sound: Predicting Specific Biological Signaling from Physics

Overview
Journal Sci Rep
Specialty Science
Date 2016 May 25
PMID 27216038
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Local changes in pH are known to significantly alter the state and activity of proteins and enzymes. pH variations induced by pulses propagating along soft interfaces (e.g. membranes) would therefore constitute an important pillar towards a physical mechanism of biological signaling. Here we investigate the pH-induced physical perturbation of a lipid interface and the physicochemical nature of the subsequent acoustic propagation. Pulses are stimulated by local acidification and propagate - in analogy to sound - at velocities controlled by the interface's compressibility. With transient local pH changes of 0.6 directly observed at the interface and velocities up to 1.4 m/s this represents hitherto the fastest protonic communication observed. Furthermore simultaneously propagating mechanical and electrical changes in the lipid interface are detected, exposing the thermodynamic nature of these pulses. Finally, these pulses are excitable only beyond a threshold for protonation, determined by the pKa of the lipid head groups. This protonation-transition plus the existence of an enzymatic pH-optimum offer a physical basis for intra- and intercellular signaling via sound waves at interfaces, where not molecular structure and mechano-enyzmatic couplings, but interface thermodynamics and thermodynamic transitions are the origin of the observations.

Citing Articles

Contribution of the Collective Excitations to the Coupled Proton and Energy Transport along Mitochondrial Cristae Membrane in Oxidative Phosphorylation System.

Nesterov S, Yaguzhinsky L, Vasilov R, Kadantsev V, Goltsov A Entropy (Basel). 2022; 24(12).

PMID: 36554218 PMC: 9778164. DOI: 10.3390/e24121813.


Acetylcholinesterase Activity Influenced by Lipid Membrane Area and Surface Acoustic Waves.

Schnitzler L, Baumgartner K, Kolb A, Braun B, Westerhausen C Micromachines (Basel). 2022; 13(2).

PMID: 35208411 PMC: 8877910. DOI: 10.3390/mi13020287.


Lipid Membrane State Change by Catalytic Protonation and the Implications for Synaptic Transmission.

Fillafer C, Koll Y, Schneider M Membranes (Basel). 2022; 12(1).

PMID: 35054529 PMC: 8781637. DOI: 10.3390/membranes12010005.


Acoustic Waves in Axonal Membrane and Caveolins are the New Targets for Pain Treatment with High Frequency Ultrasound.

Kruglikov I J Pain Res. 2020; 13:2791-2798.

PMID: 33173328 PMC: 7646452. DOI: 10.2147/JPR.S281468.


Nonlinear pulses at the interface and its relation to state and temperature.

Kang K, Schneider M Eur Phys J E Soft Matter. 2020; 43(2):8.

PMID: 32016590 DOI: 10.1140/epje/i2020-11903-x.


References
1.
Zhang C, Knyazev D, Vereshaga Y, Ippoliti E, Nguyen T, Carloni P . Water at hydrophobic interfaces delays proton surface-to-bulk transfer and provides a pathway for lateral proton diffusion. Proc Natl Acad Sci U S A. 2012; 109(25):9744-9. PMC: 3382531. DOI: 10.1073/pnas.1121227109. View

2.
Gabriel B, Teissie J . Proton long-range migration along protein monolayers and its consequences on membrane coupling. Proc Natl Acad Sci U S A. 1996; 93(25):14521-5. PMC: 26165. DOI: 10.1073/pnas.93.25.14521. View

3.
Op den Kamp J, de Gier J, Van Deenen L . Hydrolysis of phosphatidylcholine liposomes by pancreatic phospholipase A2 at the transition temperature. Biochim Biophys Acta. 1974; 345(2):253-6. DOI: 10.1016/0005-2736(74)90263-6. View

4.
Steppich D, Griesbauer J, Frommelt T, Appelt W, Wixforth A, Schneider M . Thermomechanic-electrical coupling in phospholipid monolayers near the critical point. Phys Rev E Stat Nonlin Soft Matter Phys. 2010; 81(6 Pt 1):061123. DOI: 10.1103/PhysRevE.81.061123. View

5.
Heimburg T . Mechanical aspects of membrane thermodynamics. Estimation of the mechanical properties of lipid membranes close to the chain melting transition from calorimetry. Biochim Biophys Acta. 1998; 1415(1):147-62. DOI: 10.1016/s0005-2736(98)00189-8. View