Terada Tomohiro, Inui Ken-ichi
Department of Pharmacy, Kyoto University Hospital, Faculty of Medicine, Kyoto University, Sakyo-ku, Kyoto 606-8507, Japan.
Curr Drug Metab. 2004 Feb;5(1):85-94. doi: 10.2174/1389200043489153.
Proton-coupled peptide transporters, localized at brush-border membranes of intestinal and renal epithelial cells, play important roles in protein absorption and the conservation of peptide-bound amino nitrogen. These transporters also have significant pharmacological and pharmacokinetic relevance to the transport of various peptide-like drugs such as beta-lactam antibiotics. The identification and molecular characterization of H(+)/peptide cotransporters (PEPT1 and PEPT2) have facilitated the clarification of many aspects of these transporters such as the structure/function relationship and regulation. Recent findings that intestinal PEPT1 can transport l-valine ester prodrugs such as valacyclovir provided a major step forward toward the development of novel drug delivery systems. It has been demonstrated that peptide transporters, which have a similar substrate specificity to PEPT1 and PEPT2, but possess other distinct functional properties, are localized at basolateral membranes of intestinal and renal epithelial cells. This review highlights the recent advances in our knowledge of the cellular and molecular nature of PEPT1, PEPT2 and the basolateral peptide transporters.
质子偶联肽转运体定位于肠和肾上皮细胞的刷状缘膜上,在蛋白质吸收和肽结合氨基氮的保留中发挥重要作用。这些转运体对于各种肽类药物(如β-内酰胺抗生素)的转运也具有重要的药理学和药代动力学意义。H(+)/肽共转运体(PEPT1和PEPT2)的鉴定和分子特征有助于阐明这些转运体的许多方面,如结构/功能关系和调节。最近的研究发现,肠道PEPT1可以转运缬氨酸酯前药,如伐昔洛韦,这为新型药物递送系统的开发迈出了重要一步。已经证明,具有与PEPT1和PEPT2相似底物特异性但具有其他独特功能特性的肽转运体定位于肠和肾上皮细胞的基底外侧膜上。本综述重点介绍了我们对PEPT1、PEPT2和基底外侧肽转运体的细胞和分子性质的最新认识进展。