Huennekens F M, Vitols K S, Pope L E, Fan J
Department of Molecular and Experimental Medicine, Scripps Research Institute, La Jolla, California 92037.
J Nutr Sci Vitaminol (Tokyo). 1992;Spec No:52-7. doi: 10.3177/jnsv.38.special_52.
All eukaryotic cells and some prokaryotes that are unable to synthesize folic acid utilize membrane-associated transport systems for acquisition of the pre-formed vitamin or its coenzyme forms from external sources. These transport systems, in addition to providing folates essential for cell replication, are also important because of their role in the internalization of antifolates such as Methotrexate (MTX) that are used extensively in cancer chemotherapy. Information about the components and mechanism of folate transport systems has been derived, in large part, from studies with Lactobacillus casei and L1210 mouse leukemia cells, which serve as convenient models for prokaryotes and eukaryotes, respectively. L. casei contain a single folate transport system whose Kt value (i.e., concentration for half-maximum rate of uptake) for the preferred substrate folate is in the nanomolar range. The hydrophobic membrane-associated folate transport protein (18 kDa) has been purified to homogeneity and characterized. Expression of this transporter is repressed in cells grown on high concentrations (microM) of folate. L1210 cells contain two separate transport systems for folate compounds: (1) the low affinity system (Kt values for the preferred substrates 5-methyl- and 5-formyltetrahydrofolate and MTX in the microM range); and (2) the high affinity system (Kt for folate in the nM range). Fluorescein and biotin derivatives of MTX and folate, after conversion to N-hydroxysuccinimide esters, can be attached covalently to the transporters. These probes have been used for visualizing the transporters by fluorescence and electron microscopy and for their purification to homogeneity.(ABSTRACT TRUNCATED AT 250 WORDS)
所有无法合成叶酸的真核细胞和一些原核生物利用与膜相关的转运系统从外部来源获取预先形成的维生素或其辅酶形式。这些转运系统除了提供细胞复制所必需的叶酸外,还很重要,因为它们在抗叶酸药物(如甲氨蝶呤,MTX)的内化过程中发挥作用,MTX在癌症化疗中被广泛使用。叶酸转运系统的组成和机制信息,在很大程度上来自对干酪乳杆菌和L1210小鼠白血病细胞的研究,它们分别作为原核生物和真核生物的便捷模型。干酪乳杆菌含有单一的叶酸转运系统,其对首选底物叶酸的Kt值(即摄取半最大速率时的浓度)在纳摩尔范围内。与膜相关的疏水性叶酸转运蛋白(18 kDa)已被纯化至同质并进行了表征。在高浓度(微摩尔)叶酸上生长的细胞中,这种转运蛋白的表达受到抑制。L1210细胞含有两种独立的叶酸化合物转运系统:(1)低亲和力系统(对首选底物5-甲基-和5-甲酰四氢叶酸以及MTX的Kt值在微摩尔范围内);(2)高亲和力系统(对叶酸的Kt值在纳摩尔范围内)。MTX和叶酸的荧光素和生物素衍生物在转化为N-羟基琥珀酰亚胺酯后,可以共价连接到转运蛋白上。这些探针已用于通过荧光和电子显微镜观察转运蛋白,并将其纯化至同质。(摘要截短于250字)