Valinomycin: Difference between revisions

Revision as of 12:00, 9 February 2025

A naturally occurring dodecadepsipeptide antibiotic

Structure of valinomycin

Valinomycin is a naturally occurring dodecadepsipeptide antibiotic and ionophore, produced by several species of Streptomyces. It is notable for its ability to selectively transport potassium ions across lipid membranes.

Structure

Valinomycin is a cyclic peptide composed of twelve alternating amino acids and ester groups. The structure includes three repeating units of L-valine, D-alpha-hydroxyisovaleric acid, D-valine, and L-lactic acid. This unique arrangement allows valinomycin to form a complex with potassium ions, facilitating their transport across cell membranes.

Function

Valinomycin functions as an ionophore, specifically facilitating the transport of potassium ions (K_) across lipid bilayers. It achieves this by forming a stable complex with the potassium ion, effectively shielding it from the hydrophobic environment of the lipid membrane. This property makes valinomycin a useful tool in studies of membrane potential and ion transport.

Biological Activity

Valinomycin exhibits antibiotic properties due to its ability to disrupt ion gradients across bacterial cell membranes, leading to cell death. It is particularly effective against Gram-positive bacteria. However, its use as an antibiotic is limited due to its toxicity to eukaryotic cells.

Applications

In addition to its role in biological research, valinomycin is used in biochemistry and biophysics to study ion transport and membrane dynamics. It is also employed in analytical chemistry for the selective detection of potassium ions in various samples.

Safety and Toxicity

Valinomycin is highly toxic to eukaryotic cells, including human cells, due to its ability to disrupt cellular ion homeostasis. It is classified as a hazardous substance and must be handled with care in laboratory settings.

Related pages

References

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-'''Valinomycin''' is a [[dodecadepsipeptide]] that is used by certain [[bacteria]] to facilitate the transport of [[potassium]] ions across the [[cell membrane]]. This compound is notable for its ability to selectively bind to potassium ions over other cations, such as [[sodium]] ions, due to its unique structure. Valinomycin consists of a cyclic arrangement of alternating [[amino acids]] and [[hydroxy acids]], forming a complex that encapsulates a potassium ion. This selective ion transport plays a crucial role in maintaining the [[ionic balance]] and [[membrane potential]] of cells.
+{{Short description|A naturally occurring dodecadepsipeptide antibiotic}}
+{{Use dmy dates|date=October 2023}}
-==Structure and Function==
+[[File:Valinomycin.svg|thumb|right|Structure of valinomycin]]
-Valinomycin's structure is characterized by a repeating sequence of [[L-valine]], [[D-hydroxyvaleric acid]], [[L-lactic acid]], and [[D-valine]], arranged in a cyclic fashion to form a 36-membered ring. This arrangement creates a highly specific binding site for potassium ions, which fits snugly within the ring. The complex's stability and selectivity for potassium ions are attributed to the size of the ion and the ability of the valinomycin molecule to form multiple [[hydrogen bonds]] and coordinate interactions with the potassium ion.
+'''Valinomycin''' is a naturally occurring [[dodecadepsipeptide]] antibiotic and ionophore, produced by several species of [[Streptomyces]]. It is notable for its ability to selectively transport [[potassium ions]] across lipid membranes.
-The primary function of valinomycin is to transport potassium ions across lipid bilayers. It operates by encapsulating a potassium ion within its structure, diffusing through the lipid bilayer, and releasing the ion on the opposite side. This process is driven by the concentration gradient of potassium ions across the membrane, facilitating the movement of ions from areas of high concentration to areas of low concentration without the need for ATP expenditure.
+==Structure==
+Valinomycin is a cyclic [[peptide]] composed of twelve alternating [[amino acids]] and [[ester]] groups. The structure includes three repeating units of [[L-valine]], [[D-alpha-hydroxyisovaleric acid]], [[D-valine]], and [[L-lactic acid]]. This unique arrangement allows valinomycin to form a complex with potassium ions, facilitating their transport across cell membranes.
-==Biological Significance==
+==Function==
-Valinomycin plays a significant role in the physiology of bacteria that produce it, aiding in the regulation of potassium ion concentration within the cell. This regulation is vital for maintaining the cell's osmotic balance and membrane potential, which are crucial for various cellular processes, including nutrient uptake, waste removal, and signal transduction.
+Valinomycin functions as an ionophore, specifically facilitating the transport of potassium ions (K_) across lipid bilayers. It achieves this by forming a stable complex with the potassium ion, effectively shielding it from the hydrophobic environment of the lipid membrane. This property makes valinomycin a useful tool in studies of [[membrane potential]] and ion transport.
-In addition to its role in bacteria, valinomycin has been studied for its potential applications in [[biotechnology]] and medicine. Its ability to selectively transport potassium ions across membranes has been explored for the development of [[ion-selective electrodes]] and in studies related to ion transport and membrane potential in various biological systems.
+==Biological Activity==
+Valinomycin exhibits antibiotic properties due to its ability to disrupt ion gradients across bacterial cell membranes, leading to cell death. It is particularly effective against [[Gram-positive bacteria]]. However, its use as an antibiotic is limited due to its toxicity to [[eukaryotic cells]].
-==Medical and Biotechnological Applications==
+==Applications==
-While valinomycin's natural function is beneficial to the bacteria that produce it, its potent ionophoric activity has been harnessed for various applications in research and medicine. In medical research, valinomycin is used as a tool to manipulate the ionic balance and membrane potential of cells, aiding in the study of cellular processes that depend on these factors. Its specificity for potassium ions makes it particularly useful in studies focusing on potassium ion channels and transporters.
+In addition to its role in biological research, valinomycin is used in [[biochemistry]] and [[biophysics]] to study ion transport and membrane dynamics. It is also employed in [[analytical chemistry]] for the selective detection of potassium ions in various samples.
-Furthermore, the unique properties of valinomycin have sparked interest in its potential therapeutic applications. Research is ongoing into its use in targeting diseases characterized by abnormal ion transport and membrane potential, such as certain types of [[cancer]] and [[neurological disorders]]. However, the use of valinomycin in clinical settings is limited by its toxicity and the need for targeted delivery methods to avoid adverse effects on non-target cells.
+==Safety and Toxicity==
+Valinomycin is highly toxic to eukaryotic cells, including human cells, due to its ability to disrupt cellular ion homeostasis. It is classified as a hazardous substance and must be handled with care in laboratory settings.
-==Safety and Toxicity==
+==Related pages==
-Despite its potential applications, valinomycin is highly toxic to eukaryotic cells, including human cells, due to its ability to disrupt the ionic balance and membrane potential. This disruption can lead to cell death, making valinomycin a potent cytotoxin. As such, its use is primarily restricted to laboratory research, and any potential therapeutic applications would require careful consideration of its toxicological profile and the development of strategies to mitigate its toxicity.
+* [[Ionophore]]
+* [[Streptomyces]]
+* [[Antibiotic]]
-==Conclusion==
+==References==
-Valinomycin is a fascinating molecule with unique properties that make it a valuable tool in the study of ion transport and membrane biology. Its ability to selectively transport potassium ions across cell membranes has implications for both basic research and potential therapeutic applications. However, the challenges associated with its toxicity highlight the need for continued research to fully understand and harness its potential.
+{{Reflist}}
+[[Category:Antibiotics]]
 [[Category:Ionophores]]
-[[Category:Peptides]]
+[[Category:Depsipeptides]]
-{{medicine-stub}}