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蛋白质与碳水化合物 HNK-1 的结合:共同起源?

Proteins Binding to the Carbohydrate HNK-1: Common Origins?

机构信息

Center for Molecular Neurobiology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, 20246 Hamburg, Germany.

Keck Center for Collaborative Neuroscience, Department of Cell Biology and Neuroscience, Rutgers University, 604 Allison Road, Piscataway, NJ 08854, USA.

出版信息

Int J Mol Sci. 2021 Jul 29;22(15):8116. doi: 10.3390/ijms22158116.

DOI:10.3390/ijms22158116
PMID:34360882
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8347730/
Abstract

The human natural killer (HNK-1) carbohydrate plays important roles during nervous system development, regeneration after trauma and synaptic plasticity. Four proteins have been identified as receptors for HNK-1: the laminin adhesion molecule, high-mobility group box 1 and 2 (also called amphoterin) and cadherin 2 (also called N-cadherin). Because of HNK-1's importance, we asked whether additional receptors for HNK-1 exist and whether the four identified proteins share any similarity in their primary structures. A set of 40,000 sequences homologous to the known HNK-1 receptors was selected and used for large-scale sequence alignments and motif searches. Although there are conserved regions and highly conserved sites within each of these protein families, there was no sequence similarity or conserved sequence motifs found to be shared by all families. Since HNK-1 receptors have not been compared regarding binding constants and since it is not known whether the sulfated or non-sulfated part of HKN-1 represents the structurally crucial ligand, the receptors are more heterogeneous in primary structure than anticipated, possibly involving different receptor or ligand regions. We thus conclude that the primary protein structure may not be the sole determinant for a bona fide HNK-1 receptor, rendering receptor structure more complex than originally assumed.

摘要

人类自然杀伤 (HNK-1) 碳水化合物在神经系统发育、创伤后再生和突触可塑性中发挥重要作用。有四种蛋白质已被鉴定为 HNK-1 的受体:层粘连蛋白粘附分子、高迁移率族框 1 和 2(也称为 amphoterin)和钙粘蛋白 2(也称为 N-钙粘蛋白)。由于 HNK-1 的重要性,我们想知道是否存在其他 HNK-1 受体,以及已鉴定的四种蛋白质在其一级结构上是否存在任何相似之处。选择了一组 40000 个与已知 HNK-1 受体同源的序列,用于大规模序列比对和基序搜索。尽管这些蛋白质家族中的每一个都有保守区域和高度保守的位点,但没有发现所有家族都共享的序列相似性或保守序列基序。由于尚未比较 HNK-1 受体的结合常数,并且不知道 HKN-1 的硫酸化或非硫酸化部分代表结构关键配体,因此受体的一级结构比预期的更具异质性,可能涉及不同的受体或配体区域。因此,我们得出结论,一级蛋白质结构可能不是真正的 HNK-1 受体的唯一决定因素,使得受体结构比最初假设的更复杂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80e4/8347730/a16dd39e60f7/ijms-22-08116-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80e4/8347730/9b1bc65375dc/ijms-22-08116-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80e4/8347730/7e4e06f9a0b3/ijms-22-08116-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80e4/8347730/a16dd39e60f7/ijms-22-08116-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80e4/8347730/9b1bc65375dc/ijms-22-08116-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80e4/8347730/7e4e06f9a0b3/ijms-22-08116-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80e4/8347730/a16dd39e60f7/ijms-22-08116-g003.jpg

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