Haritos A A, Caldarella J, Horecker B L
Anal Biochem. 1985 Feb 1;144(2):436-40. doi: 10.1016/0003-2697(85)90138-1.
A method was described for the isolation of peptides from rat thymus. Frozen, powdered tissue was suspended in boiling buffer to inactivate endogenous proteinases, the suspension was homogenized, and the peptides were isolated by a two-step procedure including gel filtration and purification by HPLC. The recoveries from rat thymus were, in micrograms per gram of whole tissue, 60-80 for prothymosin alpha, 50-80 for thymosin beta 4, and 20-30 for thymosin beta 10. The procedure also yielded smaller quantities of a fourth peptide, designated parathymosin alpha. The quantities of these peptides in vertebrate tissues can be evaluated by applying radioimmunoassays for prothymosin alpha and thymosin beta 4 to the boiled tissue extract.
描述了一种从大鼠胸腺中分离肽的方法。将冷冻的粉末状组织悬浮于沸腾缓冲液中以灭活内源性蛋白酶,将悬浮液匀浆,然后通过包括凝胶过滤和高效液相色谱纯化的两步法分离肽。每克全组织中,大鼠胸腺中α-原胸腺素的回收率为60 - 80微克,胸腺素β4为50 - 80微克,胸腺素β10为20 - 30微克。该方法还产生了较少量的第四种肽,命名为副胸腺素α。通过对煮沸的组织提取物应用α-原胸腺素和胸腺素β4的放射免疫测定,可以评估脊椎动物组织中这些肽的含量。