Phang J M, Valle D L, Fisher L, Granger A
Am J Physiol. 1975 Jan;228(1):23-6. doi: 10.1152/ajplegacy.1975.228.1.23.
In fetal rat calvaria, puromycin selectively inhibited the uptake of certain groups of amino acids. Puromycin treatment decreased the uptake of glycine, L-proline, and alpha-aminoisobutyric acid but was without effect on the active uptake of all other amino acids tested. In studies of alpha-aminoisobutyric acid uptake, puromycin decreased the maximal transport velocity by 70% but had no effect on the affinity of the transport system for the amino acid. With puromycin treatment, the fall-off in rates of alpha-aminoisobutyric acid uptake was first order with a half-life of 68 min. Insulin treatment increased this half-life to 118 min. These findings suggest that protein components of specific transport systems are degraded at varying rates after puromycin blockade of protein synthesis. Hormones that stimulate amino acid transport (e.g., insulin) may decrease the rate of degradation of these protein components.
在胎鼠颅骨中,嘌呤霉素选择性地抑制了某些氨基酸组的摄取。嘌呤霉素处理降低了甘氨酸、L-脯氨酸和α-氨基异丁酸的摄取,但对所测试的所有其他氨基酸的主动摄取没有影响。在α-氨基异丁酸摄取的研究中,嘌呤霉素使最大转运速度降低了70%,但对转运系统对该氨基酸的亲和力没有影响。用嘌呤霉素处理后,α-氨基异丁酸摄取速率的下降呈一级反应,半衰期为68分钟。胰岛素处理使该半衰期延长至118分钟。这些发现表明,在嘌呤霉素阻断蛋白质合成后,特定转运系统的蛋白质成分以不同速率降解。刺激氨基酸转运的激素(如胰岛素)可能会降低这些蛋白质成分的降解速率。