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2
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本文引用的文献

1
Targeting of membrane proteins to endosomes and lysosomes.将膜蛋白靶向内体和溶酶体。
Trends Cell Biol. 1994 Aug;4(8):292-7. doi: 10.1016/0962-8924(94)90220-8.
2
Neither type of mannose 6-phosphate receptor is sufficient for targeting of lysosomal enzymes along intracellular routes.两种类型的甘露糖6-磷酸受体都不足以沿细胞内途径靶向溶酶体酶。
J Cell Biol. 1996 Aug;134(3):615-23. doi: 10.1083/jcb.134.3.615.
3
In vitro binding of clathrin adaptors to sorting signals correlates with endocytosis and basolateral sorting.网格蛋白衔接蛋白与分选信号的体外结合与内吞作用及基底外侧分选相关。
EMBO J. 1996 Jun 3;15(11):2893-9.
4
Cysteine34 of the cytoplasmic tail of the cation-dependent mannose 6-phosphate receptor is reversibly palmitoylated and required for normal trafficking and lysosomal enzyme sorting.阳离子依赖性甘露糖 6-磷酸受体胞质尾的半胱氨酸 34 可发生可逆性棕榈酰化,是正常运输和溶酶体酶分选所必需的。
J Cell Biol. 1996 Feb;132(4):577-84. doi: 10.1083/jcb.132.4.577.
5
The targeting of Lamp1 to lysosomes is dependent on the spacing of its cytoplasmic tail tyrosine sorting motif relative to the membrane.Lamp1定位于溶酶体取决于其胞质尾酪氨酸分选基序相对于膜的间距。
J Cell Biol. 1996 Feb;132(4):565-76. doi: 10.1083/jcb.132.4.565.
6
The oligomeric state of 46-kDa mannose 6-phosphate receptor does not change upon intracellular recycling and binding of ligands.46-kDa 甘露糖 6-磷酸受体的寡聚状态在细胞内循环利用及与配体结合后不会改变。
Eur J Biochem. 1996 May 1;237(3):809-18. doi: 10.1111/j.1432-1033.1996.0809p.x.
7
A di-leucine motif and an upstream serine in the interleukin-6 (IL-6) signal transducer gp130 mediate ligand-induced endocytosis and down-regulation of the IL-6 receptor.白细胞介素-6(IL-6)信号转导子gp130中的双亮氨酸基序和上游丝氨酸介导配体诱导的内吞作用以及IL-6受体的下调。
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8
Ligand-induced internalization of the epidermal growth factor receptor is mediated by multiple endocytic codes analogous to the tyrosine motif found in constitutively internalized receptors.配体诱导的表皮生长因子受体内化是由多种内吞编码介导的,这些编码类似于在组成型内化受体中发现的酪氨酸基序。
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10
A Leu-Leu sequence is essential for COOH-terminal targeting signal of GLUT4 glucose transporter in fibroblasts.亮氨酸-亮氨酸序列对于成纤维细胞中葡萄糖转运蛋白4(GLUT4)的羧基末端靶向信号至关重要。
J Biol Chem. 1994 Jan 28;269(4):2353-6.

在46 kDa甘露糖6-磷酸受体胞质尾部鉴定出三个内化序列。

Identification of three internalization sequences in the cytoplasmic tail of the 46 kDa mannose 6-phosphate receptor.

作者信息

Denzer K, Weber B, Hille-Rehfeld A, Figura K V, Pohlmann R

机构信息

Georg-August-Universität Göttingen, Abt. Biochemie II, Germany.

出版信息

Biochem J. 1997 Sep 1;326 ( Pt 2)(Pt 2):497-505. doi: 10.1042/bj3260497.

DOI:10.1042/bj3260497
PMID:9291124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1218697/
Abstract

The cytoplasmic tail of the human 46 kDa mannose 6-phosphate receptor (MPR 46) is necessary for rapid internalization of the receptor and sufficient to mediate internalization of a resident plasma membrane protein. To localize the internalization sequences within the 67 amino acids of the cytoplasmic tail, the tail was progressively shortened from its C-terminus, internal deletions of between four and eight amino acids were introduced into the tail, and individual residues were substituted by alanine, glycine or serine. Three sequences were identified that contribute to the internalization of MPR 46. The first is located within the 23 juxtamembrane cytoplasmic residues of the tail. It contains four essential residues within a heptapeptide and does not resemble known internalization signals. The second sequence contains as a critical residue Tyr-45. The third region is located within the C-terminal seven residues and contains a di-leucine pair as essential residues. The first and third sequences were shown to function as autonomous internalization sequences. Substitution of critically important residues within a single internalization sequence was tolerated, with no or only a moderate decrease in the internalization rate. When essential residues from two or all three internalization sequences were substituted, however, the internalization rate was decreased by more than 60% and 90% respectively. This indicates that the autonomous internalization signals in the cytoplasmic tail of MPR 46 function in an additive manner, but are partly redundant.

摘要

人46kDa甘露糖6-磷酸受体(MPR 46)的胞质尾对于该受体的快速内化是必需的,并且足以介导驻留质膜蛋白的内化。为了定位胞质尾67个氨基酸内的内化序列,从其C末端逐渐缩短该尾,在尾中引入4至8个氨基酸的内部缺失,并将单个残基替换为丙氨酸、甘氨酸或丝氨酸。鉴定出三个有助于MPR 46内化的序列。第一个位于尾的23个近膜胞质残基内。它在一个七肽中包含四个必需残基,并且与已知的内化信号不同。第二个序列包含关键残基Tyr-45。第三个区域位于C末端的七个残基内,并且包含一对双亮氨酸作为必需残基。第一个和第三个序列被证明可作为自主内化序列发挥作用。单个内化序列内至关重要的残基被替换时仍可耐受,内化速率没有降低或仅适度降低。然而,当两个或所有三个内化序列中的必需残基被替换时,内化速率分别降低了60%以上和90%以上。这表明MPR 46胞质尾中的自主内化信号以累加方式起作用,但部分冗余。