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Electrokinetic properties of isolated cerebral-cortex synaptic vesicles
The Biochemical Journal
|December 1, 1973
Summary
Synaptic vesicle surface charge is primarily due to weak acidic groups, not sialic acid. Enzyme treatments reveal specific proteins influence vesicle mobility, indicating their role in synaptic function.
Area of Science:
- Neuroscience
- Biochemistry
- Physical Chemistry
Background:
- Synaptic vesicles are crucial for neurotransmission.
- Understanding their surface properties is key to synaptic function.
- Electrokinetic properties provide insights into surface charge and composition.
Purpose of the Study:
- To characterize the electrokinetic properties of guinea-pig cerebral cortex synaptic vesicles.
- To identify the molecular components contributing to the synaptic vesicle surface charge.
- To compare synaptic vesicle surface properties with synaptosomal membranes.
Main Methods:
- Electrophoretic mobility measurements in varying pH and ionic strength.
- Enzymatic treatments (neuraminidase, trypsin, RNase, DNase, chondroitinase ABC, hyaluronidase).
- Cation binding studies (Mn2+, Ca2+, Mg2+, Sr2+, Ba2+).
Main Results:
- Synaptic vesicles exhibited a negative electrophoretic mobility (-3.55 µm.s⁻¹.V⁻¹.cm) at pH 7.2.
- Mobility was pH and ionic strength dependent, suggesting weak acidic groups (pKa 3.0-3.8).
- Trypsin and concanavalin A treatments increased mobility; sialic acid did not significantly contribute. Divalent cations (Mn2+, Ca2+) reduced mobility more than others.
Conclusions:
- The synaptic vesicle surface is negatively charged due to weak acidic functional groups.
- Specific proteins, not sialic acid, significantly influence synaptic vesicle electrokinetic properties.
- These findings provide insights into synaptic vesicle surface composition and interactions relevant to neurotransmission.