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小蛋白的实验和计算鉴定综述。

A survey of experimental and computational identification of small proteins.

机构信息

Burnett School of Biomedical Science, University of Central Florida, 4000 Central Florida Blvd, Orlando, FL 32816, United States.

Department of Computer Science, University of Central Florida, 4000 Central Florida Blvd, Orlando, FL 32816, United States.

出版信息

Brief Bioinform. 2024 May 23;25(4). doi: 10.1093/bib/bbae345.

DOI:10.1093/bib/bbae345
PMID:39007598
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11247407/
Abstract

Small proteins (SPs) are typically characterized as eukaryotic proteins shorter than 100 amino acids and prokaryotic proteins shorter than 50 amino acids. Historically, they were disregarded because of the arbitrary size thresholds to define proteins. However, recent research has revealed the existence of many SPs and their crucial roles. Despite this, the identification of SPs and the elucidation of their functions are still in their infancy. To pave the way for future SP studies, we briefly introduce the limitations and advancements in experimental techniques for SP identification. We then provide an overview of available computational tools for SP identification, their constraints, and their evaluation. Additionally, we highlight existing resources for SP research. This survey aims to initiate further exploration into SPs and encourage the development of more sophisticated computational tools for SP identification in prokaryotes and microbiomes.

摘要

小分子蛋白(SPs)通常被定义为真核生物中小于 100 个氨基酸、原核生物中小于 50 个氨基酸的蛋白质。过去,由于定义蛋白质的大小阈值具有随意性,这些小分子蛋白一直被忽视。然而,最近的研究揭示了许多小分子蛋白的存在及其关键作用。尽管如此,小分子蛋白的鉴定及其功能的阐明仍处于起步阶段。为了为未来的小分子蛋白研究铺平道路,我们简要介绍了用于小分子蛋白鉴定的实验技术的局限性和进展。然后,我们提供了用于小分子蛋白鉴定的计算工具的概述,包括它们的局限性和评估。此外,我们还强调了现有的小分子蛋白研究资源。本综述旨在进一步探索小分子蛋白,并鼓励开发更复杂的用于原核生物和微生物组中小分子蛋白鉴定的计算工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bdc/11247407/1a77e008c2b8/bbae345f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bdc/11247407/1a77e008c2b8/bbae345f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bdc/11247407/1a77e008c2b8/bbae345f1.jpg

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本文引用的文献

1
The power of the small: the underestimated role of small proteins in bacterial and archaeal physiology.小的力量:小看了小蛋白在细菌和古菌生理学中的作用。
Curr Opin Microbiol. 2023 Dec;76:102384. doi: 10.1016/j.mib.2023.102384. Epub 2023 Sep 28.
2
Small proteins in bacteria - Big challenges in prediction and identification.细菌中的小蛋白——预测和鉴定的巨大挑战。
Proteomics. 2023 Dec;23(23-24):e2200421. doi: 10.1002/pmic.202200421. Epub 2023 Aug 23.
3
The Small-Protein Enrichment Assay (SPEA) for Analysis of Low Abundance Peptide Hormones in Plasma.
用于分析血浆中低丰度肽类激素的小蛋白富集分析(SPEA)。
Methods Mol Biol. 2023;2628:265-276. doi: 10.1007/978-1-0716-2978-9_17.
4
UniProt: the Universal Protein Knowledgebase in 2023.UniProt:2023 年的通用蛋白质知识库。
Nucleic Acids Res. 2023 Jan 6;51(D1):D523-D531. doi: 10.1093/nar/gkac1052.
5
A systematic study of HIF1A cofactors in hypoxic cancer cells.缺氧肿瘤细胞中 HIF1A 共因子的系统研究。
Sci Rep. 2022 Nov 8;12(1):18962. doi: 10.1038/s41598-022-23060-9.
6
csORF-finder: an effective ensemble learning framework for accurate identification of multi-species coding short open reading frames.csORF-finder:一种用于准确识别多物种编码短开放阅读框的有效集成学习框架。
Brief Bioinform. 2022 Nov 19;23(6). doi: 10.1093/bib/bbac392.
7
Profiling a Community-Specific Function Landscape for Bacterial Peptides Through Protein-Level Meta-Assembly and Machine Learning.通过蛋白质水平的元组装和机器学习分析细菌肽的群落特异性功能景观
Front Genet. 2022 Jul 22;13:935351. doi: 10.3389/fgene.2022.935351. eCollection 2022.
8
A systematic evaluation of the computational tools for ligand-receptor-based cell-cell interaction inference.基于配体-受体的细胞-细胞相互作用推断的计算工具的系统评价。
Brief Funct Genomics. 2022 Sep 16;21(5):339-356. doi: 10.1093/bfgp/elac019.
9
Top-Down Identification and Sequence Analysis of Small Membrane Proteins Using MALDI-MS/MS.基于 MALDI-MS/MS 的小膜蛋白从头鉴定与序列分析
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10
Short open reading frames (sORFs) and microproteins: an update on their identification and validation measures.短开放阅读框 (sORFs) 和微蛋白:它们的鉴定和验证措施的最新进展。
J Biomed Sci. 2022 Mar 17;29(1):19. doi: 10.1186/s12929-022-00802-5.