Valinomycin: Difference between revisions

From WikiMD's Wellness Encyclopedia

CSV import
CSV import
 
Line 1: Line 1:
{{Short description|A naturally occurring dodecadepsipeptide antibiotic}}
{{DISPLAYTITLE:Valinomycin}}
{{Use dmy dates|date=October 2023}}


[[File:Valinomycin.svg|thumb|right|Structure of valinomycin]]
== 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.
[[File:Valinomycin.svg|thumb|right|Chemical structure of Valinomycin]]


==Structure==
'''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]] (K_) across lipid membranes, making it a valuable tool in biochemical research and a potential therapeutic agent.
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==
== Structure ==
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.
Valinomycin is a cyclic molecule composed of 12 alternating [[amino acids]] and [[ester]] linkages. The sequence of amino acids includes both [[L-valine]] and [[D-valine]], as well as [[L-lactic acid]] and [[D-hydroxyisovaleric acid]]. This unique structure allows valinomycin to form a complex with potassium ions, stabilizing them within its hydrophilic core while presenting a hydrophobic exterior that facilitates passage through lipid bilayers.


==Biological Activity==
== Mechanism of Action ==
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]].
Valinomycin functions as an ionophore by binding potassium ions with high specificity and facilitating their transport across biological membranes. This process disrupts the [[electrochemical gradient]] of cells, which can lead to cell death. The ability of valinomycin to selectively transport potassium ions over other cations, such as [[sodium]] (Na_) or [[calcium]] (Ca__), is due to the precise fit of the potassium ion within the ionophore's cavity.


==Applications==
== Biological Activity ==
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.
Valinomycin exhibits potent antibiotic activity against a range of [[Gram-positive bacteria]] due to its ability to disrupt cellular ion gradients. However, its use as an antibiotic is limited by its toxicity to [[eukaryotic cells]], including human cells. The compound's ability to alter ion gradients also makes it a useful tool in [[biochemical research]], particularly in studies of [[mitochondrial function]] and [[membrane potential]].


==Safety and Toxicity==
== Applications ==
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.
In addition to its role in research, valinomycin has been investigated for potential therapeutic applications, including as an [[anticancer agent]]. Its ability to induce apoptosis in cancer cells by disrupting ion homeostasis is of particular interest. However, the challenge of delivering valinomycin selectively to cancer cells without affecting healthy cells remains a significant hurdle.


==Related pages==
== Related Pages ==
* [[Ionophore]]
* [[Ionophore]]
* [[Antibiotic]]
* [[Streptomyces]]
* [[Streptomyces]]
* [[Antibiotic]]
* [[Potassium channel]]
 
==References==
{{Reflist}}


[[Category:Antibiotics]]
[[Category:Antibiotics]]
[[Category:Ionophores]]
[[Category:Ionophores]]
[[Category:Depsipeptides]]
[[Category:Peptides]]

Latest revision as of 03:57, 13 February 2025


Valinomycin[edit]

Chemical 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 (K_) across lipid membranes, making it a valuable tool in biochemical research and a potential therapeutic agent.

Structure[edit]

Valinomycin is a cyclic molecule composed of 12 alternating amino acids and ester linkages. The sequence of amino acids includes both L-valine and D-valine, as well as L-lactic acid and D-hydroxyisovaleric acid. This unique structure allows valinomycin to form a complex with potassium ions, stabilizing them within its hydrophilic core while presenting a hydrophobic exterior that facilitates passage through lipid bilayers.

Mechanism of Action[edit]

Valinomycin functions as an ionophore by binding potassium ions with high specificity and facilitating their transport across biological membranes. This process disrupts the electrochemical gradient of cells, which can lead to cell death. The ability of valinomycin to selectively transport potassium ions over other cations, such as sodium (Na_) or calcium (Ca__), is due to the precise fit of the potassium ion within the ionophore's cavity.

Biological Activity[edit]

Valinomycin exhibits potent antibiotic activity against a range of Gram-positive bacteria due to its ability to disrupt cellular ion gradients. However, its use as an antibiotic is limited by its toxicity to eukaryotic cells, including human cells. The compound's ability to alter ion gradients also makes it a useful tool in biochemical research, particularly in studies of mitochondrial function and membrane potential.

Applications[edit]

In addition to its role in research, valinomycin has been investigated for potential therapeutic applications, including as an anticancer agent. Its ability to induce apoptosis in cancer cells by disrupting ion homeostasis is of particular interest. However, the challenge of delivering valinomycin selectively to cancer cells without affecting healthy cells remains a significant hurdle.

Related Pages[edit]