Functional characterization and discovery of modulators of SbMATE, the agronomically important aluminium tolerance transporter from Sorghum bicolor

被引:24
作者
Doshi, Rupak [1 ,5 ,6 ]
McGrath, Aaron P. [1 ]
Pineros, Miguel [2 ]
Szewczyk, Paul [1 ,7 ]
Garza, Denisse M. [1 ]
Kochian, Leon V. [3 ]
Chang, Geoffrey [1 ,4 ]
机构
[1] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, La Jolla, CA 92093 USA
[2] Cornell Univ, USDA ARS, Robert W Holley Ctr Agr & Hlth, Ithaca, NY 14853 USA
[3] Univ Saskatchewan, Global Inst Food Secur, Saskatoon, SK, Canada
[4] Univ Calif San Diego, Sch Med, Dept Pharmacol, La Jolla, CA 92093 USA
[5] InhibRx LLP, 11099 N Torrey Pines Rd,Suite 280, La Jolla, CA 92037 USA
[6] Univ Calif Irvine, Dept Elect Engn & Comp Sci, 2213 Engn Hall, Irvine, CA 92697 USA
[7] Sanford Burnham Prebys Med Discovery Inst, Canc Metab & Signaling Networks Program, La Jolla, CA 92037 USA
基金
澳大利亚国家健康与医学研究理事会;
关键词
TOXIC COMPOUND EXTRUSION; CITRATE TRANSPORTER; MATE MULTIDRUG; PROTEIN NORM; EFFLUX; FAMILY; GENE; IDENTIFICATION; ANTIPORTER; PUMP;
D O I
10.1038/s41598-017-18146-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
About 50% of the world's arable land is strongly acidic (pH <= 5). The low pH solubilizes root-toxic ionic aluminium (Al3+) species from clay minerals, driving the evolution of counteractive adaptations in cultivated crops. The food crop Sorghum bicolor upregulates the membrane-embedded transporter protein SbMATE in its roots. SbMATE mediates efflux of the anionic form of the organic acid, citrate, into the soil rhizosphere, chelating Al3+ ions and thereby imparting Al-resistance based on excluding Al+3 from the growing root tip. Here, we use electrophysiological, radiolabeled, and fluorescence-based transport assays in two heterologous expression systems to establish a broad substrate recognition profile of SbMATE, showing the proton and/or sodium-driven transport of (14C)-citrate anion, as well as the organic monovalent cation, ethidium, but not its divalent analog, propidium. We further complement our transport assays by measuring substrate binding to detergent-purified SbMATE protein. Finally, we use the purified membrane protein as an antigen to discover native conformationbinding and transport function-altering nanobodies using an animal-free, mRNA/cDNA display technology. Our results demonstrate the utility of using Pichia pastoris as an efficient eukaryotic host to express large quantities of functional plant transporter proteins. The nanobody discovery approach is applicable to other non-immunogenic plant proteins.
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页数:16
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