FEBS Letters | |
Isolation and sequencing of a cDNA clone encoding 107 kDa sialoglycoprotein in rat liver lysosomal membranes | |
Himeno, Masaru1  Kono, Akira2  Sakaki, Yoshiyuki3  Tanaka, Yoshitaka1  Sasaki, Hiroyuki3  Kato, Keitaro1  Noguchi, Youichiro1  Furuno, Koji1  | |
[1] Division of Physiological Chemistry, Faculty of Pharmaceutical Sciences, Kyushu University, Higashi-ku, Fukuoka, Japan;National Kyushu Cancer Center, Minami-ku, Fukuoka, Japan;Research Laboratory for Genetic Information, Kyushu University, Higashi-ku, Fukuoka, Japan | |
关键词: Sialoglycoprotein; 107-kDa; Lysosomal membrane; cDNA cloning; Amino acid sequence; LGP 107; 107-kDa sialoglycoprotein; PAGE; polyacrylamide gel electrophoresis; | |
DOI : 10.1016/0014-5793(89)80561-7 | |
学科分类:生物化学/生物物理 | |
来源: John Wiley & Sons Ltd. | |
【 摘 要 】
A cDNA for 107 kDa sialoglycoprotein (LGP 107), the major protein component of rat liver lysosomal membranes, was isolated and sequenced. The 1.8 kbp cDNA contained an open reading frame encoding a polypeptide consisting of 386 amino acid residues (M r 41914). The deduced NH2-terminal 10-residue sequence is identical with that determined for purified LGP 107. The primary structure deduced for LGP 107 contains 20 potential N-glycosylation sites and exhibits 82.5, 43 and 60% sequence similarities to mouse LAMP-1, chicken LEP 100, and a 120-kDa human lysosomal glycoprotein, respectively. Among these lysosomal glycoproteins, the amino acid sequence of the putative transmembrane segment is highly conserved. Northern blot hybridization analysis identified a single species of LGP 107 mRNA (2.1 kbp in length) in rat liver, kidney, brain, lung, spleen, heart and pancreas, although its level in pancreas was very low.
【 授权许可】
Unknown
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