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通过混合方法计算预测弗林蛋白酶裂解位点和理解疾病的潜在机制。

Computational prediction of furin cleavage sites by a hybrid method and understanding mechanism underlying diseases.

出版信息

Sci Rep. 2012;2:261. doi: 10.1038/srep00261. Epub 2012 Feb 16.

Abstract

Furin cleaves diverse types of protein precursors in the secretory pathway. The substrates for furin cleavage possess a specific 20-residue recognition sequence motif. In this report, based on the functional characterisation of the 20-residue sequence motif, we developed a furin cleavage site prediction tool, PiTou, using a hybrid method composed of a hidden Markov model and biological knowledge-based cumulative probability score functions. PiTou can accurately predict the presence and location of furin cleavage sites in protein sequences with high sensitivity (96.9%) and high specificity (97.3%). PiTou's prediction scores are biological meaningful and reflect binding strength and solvent accessibility of furin substrates. A prediction result is interpreted within cellular contexts: subcellular localisation, cellular function and interference by other dynamic protein modifications. Combining next-generation sequencing, PiTou can help with elucidating the molecular mechanism of furin cleavage-associated human diseases. PiTou has been made freely available at the associated website.

摘要

弗林蛋白酶在分泌途径中切割多种类型的蛋白前体。弗林蛋白酶切割的底物具有特定的 20 个残基识别序列基序。在本报告中,基于 20 个残基序列基序的功能特征,我们使用隐马尔可夫模型和基于生物学知识的累积概率评分函数的混合方法,开发了一种弗林蛋白酶切割位点预测工具 PiTou。PiTou 可以准确预测蛋白质序列中弗林蛋白酶切割位点的存在和位置,具有高灵敏度(96.9%)和高特异性(97.3%)。PiTou 的预测评分具有生物学意义,反映了弗林蛋白酶底物的结合强度和溶剂可及性。预测结果在细胞环境中进行解释:亚细胞定位、细胞功能和其他动态蛋白修饰的干扰。结合下一代测序,PiTou 可以帮助阐明与弗林蛋白酶切割相关的人类疾病的分子机制。PiTou 已在相关网站上免费提供。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/003f/3281273/92cd030655ae/srep00261-f1.jpg

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