摘要
目的:用荧光非天然氨基酸Aladan(Ald)改造昆虫神经肽Helicokinin Ⅰ。方法:采用多肽固相合成法合成Ald1-Heli-cokinin Ⅰ,基质辅助激光解吸电离质谱确证,经反相高效液相色谱法纯化,纯度达97%以上。结果与结论:Ald1-Helicokinin Ⅰ的合成具有快捷、简便、高效等特点,最终收率31.8%,且Ald1-Helicokinin Ⅰ可作为荧光探针,进一步研究配体跟受体的相互作用。
Objective: To modify the insect neuropeptide Helicolinin Ⅰ by fluorescent non-natural amino acid(Aladan,Ala).Methods: Ald1-Helicokinin Ⅰ could be synthesized by solid-phase peptide synthesis,confirmed by matrix-assisted laser desorptionionization mass spectrometry,purified by revered-phase high performance liquid chromatography and the purity was up to 97%.Results and discussion: The synthesis method of Ald1-Helicokinin Ⅰ is very fast,simple and high-efficient,the final product rate is 31.8%.Ald1-Helicokinin Ⅰ can be used as fluorescence probe for the further investigation on the interaction between ligand and receptor.
出处
《汕头大学医学院学报》
2010年第2期71-72,共2页
Journal of Shantou University Medical College
基金
国家自然科学基金资助项目(30672560)
广东省高等院校自然科学重点研究项目(05Z012)