## Abstract Two new ^35^S reagents were developed to radiolabel proteins. The first reagent, __N__‐succinimidyl‐4‐(methane [^35^S]sulfonylamino‐methyl)‐benzoate (SMSB), acylates the ε‐amino group of lysine residues in proteins. The second reagent, 4‐(methane [^35^S]sulfonylamino‐methyl)‐phenylpropy
Synthesis of sulfur-35 reagents for protein labeling
✍ Scribed by Sumei Ren; Paul McNamara; David Koharski; David Hesk; Scott Borges
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- French
- Weight
- 101 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
Two ^35^S reagents were developed to radiolabel proteins. The first reagent, a N‐hydroxysuccinimide (NHS) ester (SMSB), acylates the ε‐amino group of lysine residues in proteins. The second reagent, an aldehyde (MSAPPA), labels lysine residues via reductive alkylation. Comparing the two methods, the reductive alkylation method labeled proteins over a broader pH range with higher overall radiochemical yield. The biological activity of the proteins did not change after labeling with these ^35^S reagents. Copyright © 2007 John Wiley & Sons, Ltd.
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