Stable isotope substituted spin labels increase t&e resolution and sensitivity of EPR measurements. An improved synthesis of N-(l-oxy1-2,2,6,6-tetramethyl-4-piperidiny1)maleimide has been devised and utilized. This improved synthesis is accomplished in five steps instead of the normally required sev
Synthesis of two series of cysteine-specific spin labels containing a 15N substituted nitroxide
✍ Scribed by Ge Wu
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- French
- Weight
- 394 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
Synthesis of two series of spin labels with a cysteine‐reactive group, either maleimide or methanethiosulfonate, and a ^15^N substituted nitroxide separated at variable distance is reported. In the synthesis, the cysteine‐reactive groups were first incorporated into the target molecule and the ^15^N substituted nitroxide was introduced in the last step via a mild reaction without destroying the cysteine‐reactive groups. The synthetic routes described here are applicable to the synthesis of spin labels with either ^15^N substituted or “normal” ^14^N nitroxide. Spin labeling of cysteine residues in rhodopsin by the newly synthesized spin labels was also demonstrated.
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