Oct 2025· bioRxiv· Vol 22· 0 citations· 47 references
BiologyMedicine
TL;DR
This work proposes SLIDE, Sequence-free Landscape Inference for Directed Evolution, which provides an estimation for landscape ruggedness from a mutating population using only population-level phenotypic data and an estimation of mutation rate.
Abstract
Directed evolution is a method for engineering biological systems or components, such as proteins, wherein desired traits are optimised through iterative rounds of mutagenesis and selection of fit variants. The process of protein directed evolution can be envisaged as navigation over high-dimensional landscapes with numerous local maxima. The performance of any strategy in navigating such a landscape is dependent on the ruggedness of that landscape. However, this information is generally unavailable at the outset of an experiment, and cannot currently be computed using analytical methods. Here we propose SLIDE, Sequence-free Landscape Inference for Directed Evolution, which consists of two parts. First, SLIDE provides an estimation for landscape ruggedness from a mutating population using only population-level phenotypic data and an estimation of mutation rate. Ruggedness information in itself is valuable in protein design, for instance in predicting evolutionary stability. Second, SLIDE offers a framework for using the estimated ruggedness metric to select high-performing parameters for directed evolution control. Using theoretical NK landscapes and four real-world protein fitness landscapes, we demonstrate improvement upon the performance of standard selection strategies, particularly on rugged landscapes, using a pipeline that could also be combined with emerging AI-based methods for driving direction evolution.
Evolution can be thought of as taking place in a fitness landscape which maps each genotype to a fitness value. This abstraction has motivated significant efforts to quantify the statistical properties of random fitness landscapes with different amounts and types of interactions among loci—broadly referred to as epista...
Caelan Brooks, M. M. Desai, Maryn O. Carlson· bioRxiv· 0 citations
Evolutionary biology has traditionally inferred process from patterns in extant organisms and the fossil record, leaving many foundational questions constrained by their historical nature. Over the past two decades, a growing family of synthetic approaches-high-throughput mapping such as deep mutational scanning, recon...
Xue-Ying C. Li, Paco Majic, C. Westmann· Genome Biology and Evolution· 0 citations
Experimental evolution provides a reproducible testing ground for the study of adaptive evolution where the numerous degrees of freedom impacting the trajectory of evolution can be limited to their most controlled form. Evolution in a continuous culture device known as the chemostat further constrains the variables tha...
Christopher R. L. Large, Aaron W. Miller, Bryony Lynch et al.· Genetics· 0 citations
This review examines current computational strategies for exploring constrained protein fitness landscapes, including sequence-derived evolutionary descriptors, structural fitness assessment, energetic evaluation, and integrated multi-parameter scoring.
The framework is used to investigate micro-evolution of high-fitness populations and show that temporal covariance in allele-frequency changes can arise from the internal structure of a rugged genotype-phenotype map, producing signatures that resemble short-term alternating selection.
ChemTSv3 is introduced, an exploration framework with a flexible architecture that accommodates diverse design scenarios for adaptive molecular design, and shows that this flexibility enables efficient exploration across diverse design spaces, from drug-like small molecules to proteins.