Purification and interaction analyses of two human lysosomal vitamin B₁₂ transporters: LMBD1 and ABCD4

References

• Armour CM, Brebner A, Watkins D, Geraghty MT, Chan A, Rosenblatt DS. 2013. A patient with an inborn error of vitamin B12 metabolism (cblF) detected by newborn screening. Pediatrics 132:e257–e261
   Google Scholar
• Banerjee R. 2006. B12 trafficking in mammals: A for coenzyme escort service. ACS Chem Biol 1:149–159
   PubMed Web of Science ®Google Scholar
• Boulter JM, Wang DN. 2001. Purification and characterization of human erythrocyte glucose transporter in decylmaltoside detergent solution. Protein Expr Purif 22:337–348
   Google Scholar
• Chapel A, Kieffer-Jaquinod S, Sagne C, Verdon Q, Ivaldi C, Mellal M, et al. 2013. An extended proteome map of the lysosomal membrane reveals novel potential transporters. Mol Cell Proteomics 12:1572–1588
   PubMed Web of Science ®Google Scholar
• Coelho D, Kim JC, Miousse IR, Fung S, Du Moulin M, Buers I, et al. 2012. Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism. Nat Genet 44:1152–1155
   PubMed Web of Science ®Google Scholar
• Deme JC, Miousse IR, Plesa M, Kim JC, Hancock MA, Mah W, et al. 2012. Structural features of recombinant MMADHC isoforms and their interactions with MMACHC, proteins of mammalian vitamin B12 metabolism. Mol Genet Metab 107:352–362
   Google Scholar
• Duong F. 2003. Binding, activation and dissociation of the dimeric SecA ATPase at the dimeric SecYEG translocase. EMBO J 22:4375–4384
   PubMed Web of Science ®Google Scholar
• Froese DS, Gravel RA. 2010. Genetic disorders of vitamin B12 metabolism: Eight complementation groups – eight genes. Expert Rev Mol Med 12:e37
   Google Scholar
• Gherasim C, Hannibal L, Rajagopalan D, Jacobsen DW, Banerjee R. 2013a. The C-terminal domain of CblD interacts with CblC and influences intracellular cobalamin partitioning. Biochimie 95:1023–1032
   PubMed Web of Science ®Google Scholar
• Gherasim C, Lofgren M, Banerjee R. 2013b. Navigating the B12 road: Assimilation, delivery, and disorders of cobalamin. J Biol Chem 288:13186–13193
   PubMed Web of Science ®Google Scholar
• Guimaraes CP, Domingues P, Aubourg P, Fouquet F, Pujol A, Jimenez-Sanchez G, et al. 2004. Mouse liver PMP70 and ALDP: Homomeric interactions prevail in vivo. Biochim Biophys Acta 1689:235–243
   PubMed Web of Science ®Google Scholar
• Hesselink RW, Findlay JB. 2013. Expression, characterization and ligand specificity of lipocalin-1 interacting membrane receptor (LIMR). Mol Membr Biol 30:327–337
   Web of Science ®Google Scholar
• Hillebrand M, Verrier SE, Ohlenbusch A, Schafer A, Soling HD, Wouters FS, Gartner J. 2007. Live cell FRET microscopy: Homo- and heterodimerization of two human peroxisomal ABC transporters, the adrenoleukodystrophy protein (ALDP, ABCD1) and PMP70 (ABCD3). J Biol Chem 282:26997–27005
   PubMed Web of Science ®Google Scholar
• Hodgkin DC, Kamper J, Mackay M, Pickworth J, Trueblood KN, White JG. 1956. Structure of vitamin B12. Nature 178:64–66
   PubMed Web of Science ®Google Scholar
• Holzinger A, Kammerer S, Roscher AA. 1997. Primary structure of human PMP69, a putative peroxisomal ABC-transporter. Biochem Biophys Res Commun 237:152–157
   Google Scholar
• Kashiwayama Y, Seki M, Yasui A, Murasaki Y, Morita M, Yamashita Y, et al. 2009. 70-kDa peroxisomal membrane protein related protein (P70R/ABCD4) localizes to endoplasmic reticulum not peroxisomes, and NH2-terminal hydrophobic property determines the subcellular localization of ABC subfamily D proteins. Exp Cell Res 315:190–205
   Google Scholar
• Kim JC, Lee NC, Hwu PW, Chien YH, Fahiminiya S, Majewski J, et al. 2012. Late onset of symptoms in an atypical patient with the cblJ inborn error of vitamin B12 metabolism: Diagnosis and novel mutation revealed by exome sequencing. Mol Genet Metab 107:664–668
   Google Scholar
• Koutmos M, Gherasim C, Smith JL, Banerjee R. 2011. Structural basis of multifunctionality in a vitamin B12-processing enzyme. J Biol Chem 286:29780–19787
   Google Scholar
• Lewinson O, Lee AT, Locher KP, Rees DC. 2010. A distinct mechanism for the ABC transporter BtuCD-BtuF revealed by the dynamics of complex formation. Nat Struct Mol Biol 17:332–338
   Google Scholar
• Liu LX, Janvier K, Berteaux-Lecellier V, Cartier N, Benarous R, Aubourg P. 1999. Homo- and heterodimerization of peroxisomal ATP-binding cassette half-transporters. J Biol Chem 274:32738–32743
   PubMed Web of Science ®Google Scholar
• Maillard AP, Lalani S, Silva F, Belin D, Duong F. 2007. Deregulation of the SecYEG translocation channel upon removal of the plug domain. J Biol Chem 282:1281–1287
   PubMed Web of Science ®Google Scholar
• Mandava S, Makowski L, Devarapalli S, Uzubell J, Rodi DJ. 2004. RELIC – a bioinformatics server for combinatorial peptide analysis and identification of protein-ligand interaction sites. Proteomics 4:1439–1460
   PubMed Web of Science ®Google Scholar
• Miousse IR, Watkins D, Rosenblatt DS. 2011. Novel splice site mutations and a large deletion in three patients with the cblF inborn error of vitamin B12 metabolism. Mol Genet Metab 102:505–507
   PubMed Web of Science ®Google Scholar
• Myszka DG. 1999. Improving biosensor analysis. J Mol Recognit 12:279–284
   PubMed Web of Science ®Google Scholar
• Plesa M, Kim J, Paquette SG, Gagnon H, Ng-Thow-Hing C, Gibbs BF, et al. 2011. Interaction between MMACHC and MMADHC, two human proteins participating in intracellular vitamin B12 metabolism. Mol Genet Metab 102:139–148
   PubMed Web of Science ®Google Scholar
• Rath A, Glibowicka M, Nadeau VG, Chen G, Deber CM. 2009. Detergent binding explains anomalous SDS-PAGE migration of membrane proteins. Proc Natl Acad Sci USA 106:1760–1765
   PubMed Web of Science ®Google Scholar
• Rosenblatt DS, Hosack A, Matiaszuk NV, Cooper BA, Laframboise R. 1985. Defect in vitamin B12 release from lysosomes: Newly described inborn error of vitamin B12 metabolism. Science 228:1319–1321
   Google Scholar
• Rutsch F, Gailus S, Miousse IR, Suormala T, Sagne C, Toliat MR, et al. 2009. Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism. Nat Genet 41:234–239
   PubMed Web of Science ®Google Scholar
• Rutsch F, Gailus S, Suormala T, Fowler B. 2011. LMBRD1: The gene for the cblF defect of vitamin B12 metabolism. J Inherit Metab Dis 34:121–126
   PubMed Web of Science ®Google Scholar
• Schuck P. 2000. Size-distribution analysis of macromolecules by sedimentation velocity ultracentrifugation and Lamm equation modeling. Biophys J 78:1606–1619
   PubMed Web of Science ®Google Scholar
• Shani N, Jimenez-Sanchez G, Steel G, Dean M, Valle D. 1997. Identification of a fourth half ABC transporter in the human peroxisomal membrane. Hum Mol Genet 6:1925–1931
   PubMed Web of Science ®Google Scholar
• Slotboom DJ, Duurkens RH, Olieman K, Erkens GB. 2008. Static light scattering to characterize membrane proteins in detergent solution. Methods 46:73–82
   PubMed Web of Science ®Google Scholar
• Stubbe J. 1994. Binding site revealed of nature's most beautiful cofactor. Science 266:1663–1664
   PubMed Web of Science ®Google Scholar
• Tseng LT, Lin CL, Tzen KY, Chang SC, Chang MF. 2013. LMBD1 serves as a specific adaptor for insulin receptor internalization. J Biol Chem 288:32424–32432
   PubMed Web of Science ®Google Scholar
• van der Does C, De Keyzer J, Van Der Laan M, Driessen AJ. 2003. Reconstitution of purified bacterial preprotein translocase in liposomes. Methods Enzymol 372:86–98
   Google Scholar
• Vassiliadis A, Rosenblatt DS, Cooper BA, Bergeron JJ. 1991. Lysosomal cobalamin accumulation in fibroblasts from a patient with an inborn error of cobalamin metabolism (cblF complementation group): Visualization by electron microscope radioautography. Exp Cell Res 195:295–302
   Google Scholar
• Vigonsky E, Ovcharenko E, Lewinson O. 2013. Two molybdate/tungstate ABC transporters that interact very differently with their substrate binding proteins. Proc Natl Acad Sci USA 110:5440–5445
   Google Scholar
• Wanders RJ, Visser WF, Van Roermund CW, Kemp S, Waterham HR. 2007. The peroxisomal ABC transporter family. Pflugers Arch 453:719–734
   PubMed Web of Science ®Google Scholar
• Watkins D, Rosenblatt DS. 1986. Failure of lysosomal release of vitamin B12: A new complementation group causing methylmalonic aciduria (cblF). Am J Hum Genet 39:404–408
   Google Scholar
• Wojnar P, Lechner M, Merschak P, Redl B. 2001. Molecular cloning of a novel lipocalin-1 interacting human cell membrane receptor using phage display. J Biol Chem 276:20206–20212
   PubMed Web of Science ®Google Scholar
• Xu J, Liu Y, Yang Y, Bates S, Zhang JT. 2004. Characterization of oligomeric human half-ABC transporter ATP-binding cassette G2. J Biol Chem 279:19781–19789
   PubMed Web of Science ®Google Scholar