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      Novel insights into the transport mechanism of the human amino acid transporter LAT1 (SLC7A5). Probing critical residues for substrate translocation.

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          Abstract

          LAT1 (SLC7A5) is the transport competent unit of the heterodimer formed with the glycoprotein CD98 (SLC3A2). It catalyzes antiport of His and some neutral amino acids such as Ile, Leu, Val, Cys, Met, Gln and Phe thus being involved in amino acid metabolism. Interestingly, LAT1 is over-expressed in many human cancers that are characterized by increased demand of amino acids. Therefore LAT1 was recently acknowledged as a novel target for cancer therapy. However, knowledge on molecular mechanism of LAT1 transport is still scarce.

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          Author and article information

          Journal
          Biochim. Biophys. Acta
          Biochimica et biophysica acta
          Elsevier BV
          0006-3002
          0006-3002
          April 2017
          : 1861
          : 4
          Affiliations
          [1 ] Department DiBEST (Biologia, Ecologia, Scienze della Terra) Unit of Biochemistry and Molecular Biotechnology, University of Calabria, Via P. Bucci 4C, 87036 Arcavacata di Rende, Italy.
          [2 ] Dipartimento di Scienze Farmacologiche e Biomolecolari, Università degli Studi di Milano, Italy.
          [3 ] Dipartimento di Scienze Farmacologiche e Biomolecolari e Dipartimento di Scienze Biomediche e Cliniche "L. Sacco", Università degli Studi di Milano, Italy.
          [4 ] Department DiBEST (Biologia, Ecologia, Scienze della Terra) Unit of Biochemistry and Molecular Biotechnology, University of Calabria, Via P. Bucci 4C, 87036 Arcavacata di Rende, Italy. Electronic address: cesare.indiveri@unical.it.
          Article
          S0304-4165(17)30013-2
          10.1016/j.bbagen.2017.01.013
          28088504
          f39fb663-9f3e-4512-bd4d-ab4a9614c373
          History

          Docking,Liposome,Membrane transporter reconstitution,Recombinant protein expression,Site-directed mutagenesis

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