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	<id>https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=Alamethicin</id>
	<title>Alamethicin - Revision history</title>
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	<updated>2026-04-25T03:49:54Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>https://wikimd.org/index.php?title=Alamethicin&amp;diff=5629665&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=Alamethicin&amp;diff=5629665&amp;oldid=prev"/>
		<updated>2024-04-19T13:31:37Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;[[File:NRPS_basics_corrected2.jpg|NRPS basics corrected2|thumb]] [[File:Alamethicinbiosynth_corrected2.jpg|Alamethicinbiosynth corrected2|thumb|left]]    &amp;#039;&amp;#039;&amp;#039;Alamethicin&amp;#039;&amp;#039;&amp;#039; is a [[peptide]] antibiotic, produced by the fungus &amp;#039;&amp;#039;[[Trichoderma viride]]&amp;#039;&amp;#039;. It is a member of the [[peptolide]] family and is known for its ability to form [[voltage-gated ion channels]] in [[cell membranes]]. This property makes alamethicin a valuable tool for studying membrane biophysics and the function of ion channels in cells.&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
Alamethicin consists of a sequence of amino acids, making it a peptide. Its structure is characterized by a high proportion of [[alpha-helix|α-helical]] content, which is crucial for its ability to interact with lipid bilayers and form [[pore]]s or channels within membranes. The peptide is amphipathic, meaning it has both hydrophobic and hydrophilic sides, allowing it to insert itself into the lipid bilayer of cell membranes effectively.&lt;br /&gt;
&lt;br /&gt;
==Mechanism of Action==&lt;br /&gt;
The mechanism of action of alamethicin involves its insertion into the cell membrane, followed by the formation of ion channels. These channels are formed when multiple alamethicin molecules aggregate within the membrane. The formation of these channels is voltage-dependent, meaning that the channels open or close in response to changes in the electrical potential across the membrane. This property allows alamethicin to modulate the flow of ions across the membrane, affecting the cell&amp;#039;s electrical excitability and other physiological processes.&lt;br /&gt;
&lt;br /&gt;
==Applications==&lt;br /&gt;
Due to its ability to form ion channels, alamethicin has been extensively used in research to study the properties of biological membranes and ion channel function. It serves as a model compound for understanding how proteins can cross membranes and how ion channels operate. Additionally, alamethicin&amp;#039;s antimicrobial properties have prompted research into its potential use as an antibiotic or in developing new antimicrobial agents.&lt;br /&gt;
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==Safety and Toxicity==&lt;br /&gt;
While alamethicin has potential applications in medicine and research, its use is limited by its cytotoxicity. The formation of ion channels in cell membranes can disrupt normal cellular functions, leading to cell death. Therefore, the use of alamethicin in clinical settings requires careful consideration and control.&lt;br /&gt;
&lt;br /&gt;
==See Also==&lt;br /&gt;
* [[Peptide]]&lt;br /&gt;
* [[Ion channel]]&lt;br /&gt;
* [[Cell membrane]]&lt;br /&gt;
* [[Antibiotic resistance]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Peptides]]&lt;br /&gt;
[[Category:Ion channels]]&lt;br /&gt;
[[Category:Antibiotics]]&lt;br /&gt;
{{stub}}&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
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