Department of General, Inorganic and Theoretical Chemistry, University of Innsbruck, Innsbruck, Austria.
Center for Protein Assemblies (CPA), Physics Department, Chair of Theoretical Biophysics, Technical University of Munich, Garching, Germany.
MAbs. 2023 Jan-Dec;15(1):2175319. doi: 10.1080/19420862.2023.2175319.
Advances in structural biology and the exponential increase in the amount of high-quality experimental structural data available in the Protein Data Bank has motivated numerous studies to tackle the grand challenge of predicting protein structures. In 2020 AlphaFold2 revolutionized the field using a combination of artificial intelligence and the evolutionary information contained in multiple sequence alignments. Antibodies are one of the most important classes of biotherapeutic proteins. Accurate structure models are a prerequisite to advance biophysical property predictions and consequently antibody design. Specialized tools used to predict antibody structures based on different principles have profited from current advances in protein structure prediction based on artificial intelligence. Here, we emphasize the importance of reliable protein structure models and highlight the enormous advances in the field, but we also aim to increase awareness that protein structure models, and in particular antibody models, may suffer from structural inaccuracies, namely incorrect cis-amide bonds, wrong stereochemistry or clashes. We show that these inaccuracies affect biophysical property predictions such as surface hydrophobicity. Thus, we stress the importance of carefully reviewing protein structure models before investing further computing power and setting up experiments. To facilitate the assessment of model quality, we provide a tool "TopModel" to validate structure models.
结构生物学的进展以及蛋白质数据库中高质量实验结构数据的大量增加,促使许多研究致力于解决预测蛋白质结构这一重大挑战。2020 年,AlphaFold2 通过人工智能和多个序列比对中包含的进化信息的结合,彻底改变了这一领域。抗体是最重要的一类生物治疗蛋白。准确的结构模型是推进生物物理性质预测并最终进行抗体设计的前提。基于不同原理预测抗体结构的专用工具从基于人工智能的蛋白质结构预测的最新进展中受益。在这里,我们强调可靠的蛋白质结构模型的重要性,并突出该领域的巨大进展,但我们也旨在提高人们的认识,即蛋白质结构模型,特别是抗体模型,可能存在结构不准确的问题,即不正确的顺式酰胺键、错误的立体化学或冲突。我们表明,这些不准确性会影响生物物理性质预测,例如表面疏水性。因此,我们强调在进一步投入计算能力和设置实验之前,仔细审查蛋白质结构模型的重要性。为了便于评估模型质量,我们提供了一个名为“TopModel”的工具来验证结构模型。