Cysteine-accessibility analysis of transmembrane domains 11–13 of human concentrative nucleoside transporter 3
| Autor: | Jing Zhang, Tracey Tackaberry, Carol E. Cass, Taylor Raborn, Gerry Barron, Stephen A. Baldwin, James D. Young, Mabel W.L. Ritzel |
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| Rok vydání: | 2006 |
| Předmět: |
Pyrimidine
Mutant Gene Expression Saccharomyces cerevisiae Biology Biochemistry Serine chemistry.chemical_compound Humans Amino Acid Sequence Cysteine Uridine Molecular Biology Sequence Homology Amino Acid Cell Membrane Membrane Transport Proteins Cell Biology Protein Structure Tertiary Kinetics Transmembrane domain Amino Acid Substitution chemistry Mutation Symporter Nucleoside Research Article |
| Zdroj: | Biochemical Journal. 394:389-398 |
| ISSN: | 1470-8728 0264-6021 |
| DOI: | 10.1042/bj20051476 |
| Popis: | hCNT3 (human concentrative nucleoside transporter 3) is a nucleoside–sodium symporter that transports a broad range of naturally occurring purine and pyrimidine nucleosides as well as anticancer nucleoside drugs. To understand its uridine binding and translocation mechanisms, a cysteine-less version of hCNT3 was constructed and used for cysteine-accessibility and permeant-protection assays. Cysteine-less hCNT3, with 14 endogenous cysteine residues changed to serine, displayed wild-type properties in a yeast expression system, indicating that endogenous cysteine residues are not essential for hCNT3-mediated nucleoside transport. A series of cysteine-substitution mutants spanning predicted TMs (transmembrane domains) 11–13 was constructed and tested for accessibility to thiol-specific reagents. Mutants M496C, G498C, F563C, A594C, G598C and A606C had no detectable transport activity, indicating that a cysteine substitution at each of these positions was not tolerated. Two functional mutants in putative TM 11 (L480C and S487C) and four in putative TM 12 (N565C, T557C, G567C and I571C) were partially inhibited by MTS (methanethiosulphonate) reagent and high concentrations of uridine protected against inhibition, indicating that TMs 11 and 12 may form part of the nucleoside translocation pathway. The lack of accessibility of MTS reagents to TM 13 mutants suggests that TM 13 is not exposed to the nucleoside translocation pathway. Furthermore, G567C, N565C and I571C mutants were only sensitive to MTSEA (MTS-ethylammonium), a membranepermeant thiol reagent, indicating that these residues may be accessible from the cytoplasmic side of the membrane, providing evidence in support of the predicted orientation of TM 12 in the current putative topology model of hCNT3. |
| Databáze: | OpenAIRE |
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