Zolotarev Iu A, Dadaian A K, Vas'kovskiĭ B V, Kost N V, Garanin S K, Makarenkova V P, Miasoedov N F
Institute of Molecular Genetics, Russian Academy of Sciences, pl. Akademika Kurchatova 2, Moscow, Russia.
Bioorg Khim. 2000 Jul;26(7):512-5.
A [3H]Dalargin preparation with a molar radioactivity of 52 Ci/mmol was obtained by the high temperature solid-state catalytic isotope exchange (HSCIE) of tritium for hydrogen at 150 degrees C. This tritium-labeled peptide was shown to completely retain its biological activity in the test of binding to opioid receptors from rat brain. The dissociation constant of the Dalargin-opioid receptor complex was found to be 4.3 nM. The dependencies of the chemical yield and the molar radioactivity on the reaction time and temperature of HSCIE were determined. The activation energy of the HSCIE reaction for the peptide was calculated to be 32 kcal/mol. The amino acid analysis showed that tritium is distributed between all the amino acid residues of [3H]Dalargin at the HSCIE reaction, with the temperature growth significantly increasing the total tritium incorporation and, especially, enhancing the radioactivity incorporation into aromatic residues.
通过在150℃下进行氚与氢的高温固态催化同位素交换(HSCIE),获得了摩尔放射性为52 Ci/mmol的[³H]达拉argin制剂。在与大鼠脑阿片受体结合的测试中,这种氚标记的肽被证明完全保留了其生物活性。发现达拉argin - 阿片受体复合物的解离常数为4.3 nM。确定了化学产率和摩尔放射性对HSCIE反应时间和温度的依赖性。计算得出该肽的HSCIE反应活化能为32 kcal/mol。氨基酸分析表明,在HSCIE反应中,氚分布在[³H]达拉argin的所有氨基酸残基之间,随着温度升高,总氚掺入量显著增加,尤其是增强了芳香族残基中的放射性掺入。