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	<title>Translations:Protein/59/en - Revision history</title>
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	<updated>2026-04-20T14:23:35Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<title>FuzzyBot: Importing a new version from external source</title>
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		<updated>2024-02-23T07:36:06Z</updated>

		<summary type="html">&lt;p&gt;Importing a new version from external source&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;For natural proteins, a series of purification steps may be necessary to obtain protein sufficiently pure for laboratory applications. To simplify this process, [[genetic engineering]] is often used to add chemical features to proteins that make them easier to purify without affecting their structure or activity. Here, a &amp;quot;tag&amp;quot; consisting of a specific amino acid sequence, often a series of [[histidine]] residues (a &amp;quot;[[His-tag]]&amp;quot;), is attached to one terminus of the protein. As a result, when the lysate is passed over a chromatography column containing [[nickel]], the histidine residues ligate the nickel and attach to the column while the untagged components of the lysate pass unimpeded. A number of different tags have been developed to help researchers purify specific proteins from complex mixtures.&lt;/div&gt;</summary>
		<author><name>FuzzyBot</name></author>
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