An open-source automated PEG precipitation assay to measure the relative solubility of proteins with low material requirement
Supplemental record retained to make the downloaded paper corpus fully navigable.
- Year
- —
- Skill
- medium
- Docs
- moderate
- Rubric
- 3.4 / 5
Implementation assessment
Scoring by criterion
Scores describe accessibility and implementation characteristics reported in the reviewed source. They are not a measure of scientific quality.
Resolution
No clear feature-size or precision evidence found.
Scalability/Throughput
Evidence of parallel, plate-scale, multi-head, or unattended operation.
Build and Part Sourcing Complexity
Mix of common parts and custom/printed components.
Skill Complexity
Build/operation described as low-skill or basic assembly.
Equipment/Cosumable/Facility Requirement Accessibility
Equipment requirements not explicit; assigned moderate default.
Application Level
Presented as modular or usable across multiple workflows.
Accessibility to documentation
Some open documentation or files are available.
Validation/Troubleshooting Complexity
Validation includes standards, benchmarking, replicates, or multi-condition tests.
Speed/Cycle Time
Speed evidence suggests rapid, real-time, or automated operation.
Build Time
Build time not reported; assigned neutral score.
Record metadata
Publication data
Crossref and OpenAlex
Publication record
Abstract
The solubility of proteins correlates with a variety of their properties, including function, production yield, pharmacokinetics, and formulation at high concentrations. High solubility is therefore a key requirement for the development of protein-based reagents for applications in life sciences, biotechnology, diagnostics, and therapeutics. Accurate solubility measurements, however, remain challenging and resource intensive, which limits their throughput and hence their applicability at the early stages of development pipelines, when long-lists of candidates are typically available in minute amounts. Here, we present an automated method based on the titration of a crowding agent (polyethylene glycol, PEG) to quantitatively assess relative solubility of proteins using about 200 µg of purified material. Our results demonstrate that this method is accurate and economical in material requirement and costs of reagents, which makes it suitable for high-throughput screening. This approach is freely-shared and based on a low cost, open-source liquid-handling robot. We anticipate that this method will facilitate the assessment of the developability of proteins and make it substantially more accessible.
Bibliographic details
Access and metrics
Topics and keywords
Perspective and practical signals
Why it matters
Supplemental record retained to make the downloaded paper corpus fully navigable.
Limitations
Metadata is limited to the download manifest and title-derived mapping.