Presynaptic vesicles, exocytosis, membrane fusion and basic physical forces
1University Department of Neurology, Sestre Milosrdnice University Hospital, Zagreb, Croatia. zlatko.trkanjec@zg.tel.hr
Medical Hypotheses
|May 8, 2001
Summary
This study proposes a physical model for vesicle release and membrane fusion, utilizing electrostatic and surface tension forces. The model explains how charge dynamics during action potentials drive presynaptic vesicle fusion with the nerve terminal membrane.
Area of Science:
- Neuroscience
- Biophysics
- Cell Biology
Background:
- Vesicle release from presynaptic nerve endings and membrane fusion are critical cellular processes.
- Existing models often involve complex molecular machinery.
- A fundamental physical explanation is lacking for the rapid kinetics observed.
Purpose of the Study:
- To present a theoretical hypothesis explaining vesicle release and membrane fusion.
- To elucidate the roles of electrostatic and surface tension forces in these processes.
- To propose a unified physical mechanism applicable to various membrane fusion events.
Main Methods:
- Theoretical modeling based on fundamental physical forces.
- Analysis of transmembrane resting potential and electrostatic charge distribution in lipid bilayers.
- Consideration of membrane dynamics during endocytosis and exocytosis.
Main Results:
- The hypothesis posits differential electrostatic charges on inner and outer lipid layers of membranes and vesicles.
- Action potentials induce charge attraction, bringing vesicles and cell membranes into close contact.
- Surface tension forces then drive membrane fusion to minimize interfacial energy.
Conclusions:
- Fundamental physical forces (electrostatic and surface tension) can adequately explain rapid vesicle release and membrane fusion.
- This physical model offers a potentially universal mechanism for exocytic and membrane fusion processes.
- The proposed mechanism highlights the efficiency and speed achievable through basic physical principles.
Related Concept Videos
Exocytosis
Exocytosis is used to release material from cells. Like other bulk transport mechanisms, exocytosis requires energy.
Exocytosis
Exocytosis is a process that releases molecules outside the cell. Like other bulk transport mechanisms, exocytosis requires energy.
Exocytosis is the opposite of endocytosis, which brings molecules inside the cell. Sometimes, the released materials are signaling molecules. For example, neurons typically use exocytosis to release neurotransmitters. Cells also use exocytosis to insert proteins such as ion channels into their cell membranes, secrete proteins for use in the extracellular matrix, or...
Exocytosis is the opposite of endocytosis, which brings molecules inside the cell. Sometimes, the released materials are signaling molecules. For example, neurons typically use exocytosis to release neurotransmitters. Cells also use exocytosis to insert proteins such as ion channels into their cell membranes, secrete proteins for use in the extracellular matrix, or...
Fusion of Secretory Vesicles with the Plasma Membrane
Proteins and neurotransmitters in secretory vesicles can be released from a cell upon vesicle docking, priming, and fusion with the plasma membrane. Vesicles are docked and primed in preparation for the quick exocytosis of their contents in response to a stimulus. The fusion process is mainly carried out by a SNAP Receptor or SNARE complex, consisting of synaptobrevin, syntaxin-1, and SNAP-25.
In 1993, Jim Rothman proposed that the antiparallel pairing of vesicular and transmembrane SNAREs, or...
In 1993, Jim Rothman proposed that the antiparallel pairing of vesicular and transmembrane SNAREs, or...
SNAREs and Membrane Fusion
Once a transport vesicle has recognized its target organelle, the vesicular membrane needs to fuse with the target membrane to unload the cargo. Transmembrane proteins called SNAREs present on organelle membranes and their vesicles, mediate vesicle fusion.
SNAREs exist in pairs that symmetrically interact and catalyze the fusion of the lipid bilayers in vesicle and target organelle. v-SNARE in the vesicle membrane are single polypeptide chains that bind to a complementary t-SNARE, composed of 2...
SNAREs exist in pairs that symmetrically interact and catalyze the fusion of the lipid bilayers in vesicle and target organelle. v-SNARE in the vesicle membrane are single polypeptide chains that bind to a complementary t-SNARE, composed of 2...
Chemical Synapses
Chemical synapses are specialized sites between two neurons or between a neuron and a non-neuronal cell like a muscle, glandular or sensory cell.
Because chemical synapses depend on the release of neurotransmitter molecules from synaptic vesicles to pass on their signal, there is an approximately one millisecond delay between when the axon potential reaches the presynaptic terminal and when the neurotransmitter leads to opening of postsynaptic ion channels. Additionally, this signaling is...
Because chemical synapses depend on the release of neurotransmitter molecules from synaptic vesicles to pass on their signal, there is an approximately one millisecond delay between when the axon potential reaches the presynaptic terminal and when the neurotransmitter leads to opening of postsynaptic ion channels. Additionally, this signaling is...
Chemical Synapses
Chemical synapses are specialized sites between two neurons or between a neuron and a non-neuronal cell like a muscle, glandular or sensory cell.
Because chemical synapses depend on the release of neurotransmitter molecules from synaptic vesicles to pass on their signal, there is an approximately one millisecond delay between when the axon potential reaches the presynaptic terminal and when the neurotransmitter leads to opening of postsynaptic ion channels. Additionally, this signaling is...
Because chemical synapses depend on the release of neurotransmitter molecules from synaptic vesicles to pass on their signal, there is an approximately one millisecond delay between when the axon potential reaches the presynaptic terminal and when the neurotransmitter leads to opening of postsynaptic ion channels. Additionally, this signaling is...


