元酶:用于任务适应性再设计的元泛酶学习

Jiangbin Zheng, Han Zhang, Qianqing Xu, An-Ping Zeng, Stan Z. Li
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引用次数: 0

摘要

然而,由于缺乏全面的基准和酶设计任务的复杂性,这一领域面临着挑战,导致系统研究十分匮乏。因此,在更广泛的蛋白质领域,计算酶设计相对被忽视,仍处于早期阶段。在这项工作中,我们通过引入分阶段统一的酶设计框架 MetaEnzyme 来应对这些挑战。我们首先采用跨模态结构到序列的转换架构,作为特征驱动的起点,以获得最初的健壮蛋白质表征。随后,我们利用领域自适应技术在低资源条件下推广特定的酶设计任务。MetaEnzyme 专注于三个基本资源酶再设计任务:功能设计(FuncDesign)、突变设计(MutDesign)和序列生成设计(SeqDesign)。通过新颖的统一范式和增强的表示能力,MetaEnzymed 演示了对各种酶设计任务的适应性,并取得了杰出的成果。湿实验室实验进一步验证了这些发现,加强了重新设计过程的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MetaEnzyme: Meta Pan-Enzyme Learning for Task-Adaptive Redesign
Enzyme design plays a crucial role in both industrial production and biology. However, this field faces challenges due to the lack of comprehensive benchmarks and the complexity of enzyme design tasks, leading to a dearth of systematic research. Consequently, computational enzyme design is relatively overlooked within the broader protein domain and remains in its early stages. In this work, we address these challenges by introducing MetaEnzyme, a staged and unified enzyme design framework. We begin by employing a cross-modal structure-to-sequence transformation architecture, as the feature-driven starting point to obtain initial robust protein representation. Subsequently, we leverage domain adaptive techniques to generalize specific enzyme design tasks under low-resource conditions. MetaEnzyme focuses on three fundamental low-resource enzyme redesign tasks: functional design (FuncDesign), mutation design (MutDesign), and sequence generation design (SeqDesign). Through novel unified paradigm and enhanced representation capabilities, MetaEnzyme demonstrates adaptability to diverse enzyme design tasks, yielding outstanding results. Wet lab experiments further validate these findings, reinforcing the efficacy of the redesign process.
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