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	<title>Ni-NTA-Gold Nanoparticles - Revision history</title>
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	<updated>2026-10-19T21:55:29Z</updated>
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		<title>Paul.xu: Created page with &quot;== Synthesis of Ni-NTA-5 nm Gold Nanoparticles.&lt;br&gt; ==  &lt;br&gt;  http://www.google.com/patents/US20120244075  The Ni-NTA-5 nm gold nanoparticles were prepared by the synthesis of 5 ...&quot;</title>
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		<updated>2014-09-25T14:26:26Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;== Synthesis of Ni-NTA-5 nm Gold Nanoparticles.&amp;lt;br&amp;gt; ==  &amp;lt;br&amp;gt;  http://www.google.com/patents/US20120244075  The Ni-NTA-5 nm gold nanoparticles were prepared by the synthesis of 5 ...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;== Synthesis of Ni-NTA-5 nm Gold Nanoparticles.&amp;lt;br&amp;gt; ==&lt;br /&gt;
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http://www.google.com/patents/US20120244075&lt;br /&gt;
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The Ni-NTA-5 nm gold nanoparticles were prepared by the synthesis of 5 nm nitrilotriacetic acid (NTA) gold nanoparticles followed by chelating to Ni2+. In addition to Ni2+, NTA gold nanoparticles can also chelate to other metal ions such as by way of example only, Cu2+ and Zn2+. &amp;lt;br&amp;gt;&lt;br /&gt;
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The 5 nm NTA gold nanoparticles were synthesized by adding&amp;#039;&amp;#039;&amp;#039;sodium borohydride, NaBH4&amp;#039;&amp;#039;&amp;#039; (114 mg, 3 mmol) in 5 mL of deionized water to a mixture of &amp;#039;&amp;#039;&amp;#039;Gold(III) chloride trihydrate, HAuCl4·xH2O&amp;#039;&amp;#039;&amp;#039; (118 mg, 0.3 mmol, G4022-1G, $105.5), &amp;#039;&amp;#039;&amp;#039;2-(2′-(2″-methoxyethoxy)ethoxy)ethane thiol&amp;#039;&amp;#039;&amp;#039; (15 mg, 0.08 mmol) and &amp;#039;&amp;#039;&amp;#039;5-(6′-mercaptohexanoylamino)-1-carboxypentylimino diacetate trisodium salt&amp;#039;&amp;#039;&amp;#039; (32 mg, 0.08 mmol) in 55 mL of 6:1:1 methanol/acetic acid/H2O with rapid stirring. After two hours of stirring, the 5 nm NTA gold nanoparticles were pelleted down by centrifugation. The crude gold nanoparticles were redissolved in deionized water, and purified by filtration through a membrane with MW cut-off of 30,000. The purified NTA gold nanoparticles were diluted to 1 L with 50 mM MOPs, pH7.9. 600 μL of 0.2 N NiSO4 solution was added to the NTA gold solution with stirring. After two hours stirring, the solution was concentrated with membrane filtration (MWCO=30,000) and chromatographed over a desalting column, e.g., GH-25. The gold fractions were collected as Ni-NTA-5 nm gold. The prepared Ni-NTA-5 nm gold nanoparticles were nearly monodispersed, and its electron micrograph is shown in FIG. 2.&amp;lt;br&amp;gt;&amp;lt;br&amp;gt;&lt;br /&gt;
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Sensitive Detection of a His-Tagged Protein Using Blots.&lt;br /&gt;
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The 6x-His-tagged protein, ATF-1, was spotted onto nitrocellulose, depositing (from left to right) 100 ng, 50 ng, 10 ng, 5 ng, 1 ng, and 0.5 ng per spot. A second row of control proteins (all spots identical), E. Coli extract (1 μL of 2.03 mg/ml total protein, 2.03 μg per spot), was spotted directly below the test target ATF-1 protein spots. The blot was blocked with 5% non-fat dry milk in 20 mM Tris, 0.15 M NaCl, pH7.6 containing 0.1% (w/v) Tween® 20 (TBST), and incubated 30 min. with the Ni-NTA-5 nm gold nanoparticles in 50 mM MOPs pH7.9 (OD280 nm=1.5). The blot was then washed with 10 mM imidazole in TB ST for 2 min. After washing the membrane three times with water, the spots were catalytically enhanced with &amp;#039;&amp;#039;&amp;#039;Gold Enhance EM&amp;#039;&amp;#039;&amp;#039; (Nanoprobes) for 9 min. The membrane was then washed with water and dried. All target spots could be detected (FIG. 3), whereas all control spots were negative, indicating a sensitivity of 0.5 ng.&amp;lt;br&amp;gt;&amp;lt;br&amp;gt;&lt;br /&gt;
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Detecting Polyhistidine Tagged Proteins on Western Blots.&lt;br /&gt;
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As shown in FIG. 6, the indicated amounts of purified 6x-His-tagged ATF-1 (34 kDa), 6x-His-tagged YY1 (68 kDa), 6x-His-tagged Src (61.7 kDa) mixed with crude extract from E. coli cells, and the crude extract from E. coli cells (1.25 μg total protein per lane) were applied to a 4-15% SDS-polyacrylamide gel. The 6xHis Protein Ladder (6xHPL) consists of five 6x-His-tagged proteins ranging from 15 to 100 kDa. It was loaded as a molecular weight standard, and as a positive control for western blotting. After electrophoresis and Western transfer, 6x-His-tagged proteins were detected by Ni-NTA-5 nm gold nanoparticles followed by GoldEnhance EM (Nanoprobes Inc., catalog #2113). The Ni-NTA-5 nm gold nanoparticles selectively detected all poly His-tagged proteins including 6xHis Protein Ladder, 6x-His-tagged ATF-1, 6x-His-tagged YY1, and 6x-His-tagged Src, but have no detectable binding to the crude extract from E. coli cells.&amp;lt;br&amp;gt;&lt;br /&gt;
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[[Category:Protocols]]&lt;/div&gt;</summary>
		<author><name>Paul.xu</name></author>
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