Kilinc Mesih, Jia Kejue, Jernigan Robert L
Bioinformatics and Computational Biology Program, Iowa State University, Ames, IA 50011, USA; Roy J. Carver Department of Biochemistry, Biophysics and Molecular Biology, Iowa State University, Ames, IA 50011, USA.
Roy J. Carver Department of Biochemistry, Biophysics and Molecular Biology, Iowa State University, Ames, IA 50011, USA; Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06511, USA.
Curr Opin Struct Biol. 2025 Feb;90:102984. doi: 10.1016/j.sbi.2025.102984. Epub 2025 Jan 27.
There is an ever-increasing need for accurate and efficient methods to identify protein homologs. Traditionally, sequence similarity-based methods have dominated protein homolog identification for function identification, but these struggle when the sequence identity between the pairs is low. Recently, transformer architecture-based deep learning methods have achieved breakthrough performances in many fields. One type of model that uses transformer architecture is the protein language model (pLM). Here, we describe methods that use pLMs for protein homolog identification intended for function identification and describe their strengths and weaknesses. Several important ideas emerge, such as filtering the substitution matrix generated from embeddings, selecting specific pLM layers for specific purposes, compressing the embeddings, and dividing proteins into domains before searching for homologs that improve remote homolog detection accuracy considerably. All of these approaches produce huge numbers of new homologs that can reliably extend the reach of protein relationships for a deeper understanding of evolution and many other problems.
对准确且高效的蛋白质同源物识别方法的需求日益增长。传统上,基于序列相似性的方法在用于功能识别的蛋白质同源物识别中占据主导地位,但当序列对之间的序列同一性较低时,这些方法就会遇到困难。最近,基于Transformer架构的深度学习方法在许多领域都取得了突破性的表现。一种使用Transformer架构的模型是蛋白质语言模型(pLM)。在这里,我们描述了使用pLM进行旨在功能识别的蛋白质同源物识别的方法,并描述了它们的优缺点。出现了几个重要的想法,例如过滤从嵌入生成的替换矩阵、为特定目的选择特定的pLM层、压缩嵌入以及在搜索同源物之前将蛋白质划分为结构域,这些方法可显著提高远程同源物检测的准确性。所有这些方法都产生了大量新的同源物,这些同源物可以可靠地扩展蛋白质关系的范围,以便更深入地理解进化和许多其他问题。