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High Throughput Screening and Selection Methods for Directed Enzyme Evolution
DOI:10.1021/ie503060a.png)
Abstract
En 中文
Successful evolutionary enzyme engineering requires a high throughput screening or selection method, which considerably increases the chance of obtaining desired properties and reduces the time and cost. In this review, a series of high throughput screening and selection methods are illustrated With significant and recent examples. These high throughput strategies are also discussed with an emphasis on compatibility with phenotypic analysis during directed enzyme evolution. Lastly, certain limitations of current methods, as well as future developments, are briefly summarized.
Keywords:
IN-VITRO SELECTION
RESONANCE ENERGY-TRANSFER
CELL-SURFACE DISPLAY
RIBOSOME DISPLAY
PHAGE DISPLAY
PROTEIN
SYSTEM
IDENTIFICATION
BIOCATALYSTS
SPECIFICITY
AI Summary
Key information extracted from the uploaded paper, including a brief overview, abstract, background, key highlights, visual analysis, and future outlook.
Journal
I
IF:
3.9
Papers:
4.0W
Citations:
9.6W
Organization
Cited Papers
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BMJ Open
IF0
Ribosome display:: selecting and evolving proteins in vitro that specifically bind to a target
NATURE METHODS
IF32.1
Microfluidic high-throughput culturing of single cells for selection based on extracellular metabolite production or consumption
NATURE BIOTECHNOLOGY
IF41.7
Higher throughput bioanalysis by automation of a protein precipitation assay using a 96-well format with detection by LC-MS/MS
ANALYTICAL CHEMISTRY
IF6.7
Imaging protein-protein interactions using fluorescence resonance energy transfer microscopy
METHODS
IF4.3

