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Custom Enzymes

Custom enzymes by Creative Enzymes.

Enzymes, the catalysts of biological systems, have become indispensable for research and diagnostic applications. From research to diagnostics, these biocatalysts catalyze a wide range of chemical transformations with unprecedented specificity and efficiency. However, natural enzymes are not always a perfect fit for the applications they serve. That's where custom enzymes come in, bridging the gap between natural function and practical need. Tailored enzymes, modified or engineered to precise specifications, offer transformative potential across multiple disciplines.

At Creative Enzymes, we deliver high-quality, custom-designed enzymes and enzyme blends tailored to specific needs that not only enhance scientific discovery, but also open doors to innovation in diagnostics, molecular biology and medical research.

The Need for Custom Enzymes

The natural world provides a diverse enzyme toolkit; however, natural enzymes often fail to meet the rigorous demands of research, diagnostic or therapeutic applications. Factors such as thermal instability, pH sensitivity, suboptimal substrate specificity, and low catalytic efficiency can limit their performance in non-biological environments. Custom enzymes address these shortcomings through targeted modifications, improving performance while expanding the range of applications.

Strategies for Custom Enzyme Design

Custom enzyme design encompasses multiple strategies, each tailored to achieve specific functional goals. These approaches can be broadly categorized as follows:

Directed Evolution

In cases where structural knowledge is limited, directed evolution provides a powerful alternative. This method mimics natural selection in the laboratory by creating enzyme libraries through random mutagenesis or recombination. Variants are screened for desired traits, and the best performers are further refined through iterative cycles of mutation and selection.

Directed evolution has been pivotal in creating enzymes for sustainable biofuel production, pharmaceutical synthesis, and even novel biomaterials.

Rational Design

Rational design relies on detailed knowledge of an enzyme's structure and mechanism. Researchers use computational tools and structural biology techniques to predict how changes to amino acid sequences will affect an enzyme's activity, stability, or specificity.

For example, introducing specific mutations in the active site can improve substrate binding, thereby increasing catalytic efficiency. Similarly, modifications in peripheral regions can improve the stability of an enzyme at high temperatures or other challenging conditions.

De Novo Design

The most ambitious approach to creating custom enzymes is de novo design, in which entirely new enzymes are created from scratch. Using computational models, scientists design enzymes with customized active sites optimized for specific reactions. While challenging, this technique has led to breakthroughs, including enzymes for reactions not known to occur in nature.

Chemical Modifications

Chemical modifications, such as conjugation of enzymes with polymers, cofactors or nanoparticles, can further enhance enzyme performance. These modifications can improve thermal stability, reduce immunogenicity (in therapeutic contexts), or allow site-specific immobilization for industrial use.

Strategies for custom enzyme design: enzyme redesign, directed evolution, semi-rational design, rational design, and de novo design.Figure. 1: Enzyme design approaches. (a) The fitness landscape map of an enzyme shows the relationship between different variants of an enzyme and their fitness. (b) Directed evolution mimics the natural evolution process to improve the function of proteins through multiple rounds of random mutation, screening and selection. (c) In the semi-rational design approach, the key sites identified based on enzyme structures are mutated with saturation mutagenesis to improve the enzyme function. (d) In the rational design approach, the sites identified based on the dynamic structures and catalytic mechanism of enzyme are mutated to improve protein function. (e) De novo design methods are used to construct protein backbones from scratch to generate protein structures with new functions. (Zhou and Huang, 2024)

Custom Enzyme Blends

Custom enzyme blends refer to the strategic combination of multiple enzymes to perform specific functions or achieve desired results. Unlike single enzymes that catalyze individual reactions, enzyme blends are designed to work synergistically to provide increased efficiency, functionality and versatility.

For research and diagnostic purposes, enzyme blends can be optimized for specificity, activity, and stability to meet specific experimental conditions or diagnostic requirements. These blends are particularly valuable in applications requiring sequential reactions, multi-step processes, or compatibility with specific substrates.

Applications of Custom Enzymes for Research & Diagnostic Use

Custom enzymes, designed to meet specific requirements, are invaluable in research and diagnostics due to their tailored activity, stability, and specificity. Their applications span diverse fields, including molecular biology, proteomics, clinical diagnostics, and biotechnology.

Molecular Biology Applications

  • PCR and qPCR: Modified DNA polymerases enhance amplification efficiency, fidelity, and speed in polymerase chain reactions, enabling applications like genotyping and gene expression studies.
  • Gene Editing: Custom nucleases (e.g., CRISPR-associated enzymes) enable precise genome editing, aiding functional genomics and therapeutic research.
  • Cloning: Tailored restriction enzymes and ligases improve vector design and DNA assembly efficiency.

Proteomics and Protein Engineering

  • Protein Digestion: Modified proteases with specific cleavage preferences enhance peptide mapping and mass spectrometry analysis.
  • Post-Translational Modification Analysis: Tailored kinases, phosphatases, and glycosidases enable the study of protein modifications like phosphorylation and glycosylation.

Clinical Diagnostics

  • Biomarker Detection: Enzymes like peroxidases and alkaline phosphatases are customized for immunoassays, including ELISA and lateral flow tests, to improve signal generation and stability.
  • Point-of-Care Testing: Tailored enzymes enhance the accuracy and speed of rapid diagnostic tests for infectious diseases, metabolic disorders, and cardiovascular conditions.
  • Nucleic Acid Detection: Custom reverse transcriptases and polymerases improve sensitivity in diagnostic applications such as COVID-19 detection and cancer mutation screening.

Environmental and Food Testing

  • Pathogen Detection: Enzymes designed for rapid amplification and detection are used in identifying foodborne pathogens and contaminants.
  • Residue Analysis: Tailored enzymes assist in detecting pesticides, antibiotics, and allergens in food and environmental samples.

Development of Research Tools

  • Biosensors: Enzymes engineered for high specificity and stability are incorporated into biosensors to detect metabolites, ions, and environmental pollutants.
  • Signal Amplification: Customized enzymes improve sensitivity in fluorescence, colorimetric, or chemiluminescent assays, making them more robust for research and high-throughput screening.

Applications of custom enzymes in the research and diagnostic fields.

Custom enzymes have revolutionized research and diagnostics by providing unparalleled precision, efficiency and flexibility. At Creative Enzymes, we provide expertly engineered custom enzymes to meet your specific needs. Contact us today to find the best solutions for your research and diagnostic applications!

Reference:

  1. Zhou J, Huang M. Navigating the landscape of enzyme design: from molecular simulations to machine learning. Chem Soc Rev. 2024;53(16):8202-8239.
Catalog Product Name EC No. CAS No. Source Price
EXWM-2463 kaempferol 3-O-galactosyltransferase EC 2.4.1.234 Inquiry
EXWM-2462 initiation-specific α-1,6-mannosyltransferase EC 2.4.1.232 346003-17-6 Inquiry
EXWM-2461 α,α-trehalose phosphorylase (configuration-retaining) EC 2.4.1.231 Inquiry
EXWM-2460 kojibiose phosphorylase EC 2.4.1.230 206566-36-1 Inquiry
EXWM-2459 sphingosine β-galactosyltransferase EC 2.4.1.23 9032-90-0 Inquiry
EXWM-2458 [Skp1-protein]-hydroxyproline N-acetylglucosaminyltransferase EC 2.4.1.229 256531-81-4 Inquiry
EXWM-2457 lactosylceramide 4-α-galactosyltransferase EC 2.4.1.228 52725-57-2 Inquiry
EXWM-2456 undecaprenyldiphospho-muramoylpentapeptide β-N-acetylglucosaminyltransferase EC 2.4.1.227 60976-26-3 Inquiry
EXWM-2455 N-acetylgalactosaminyl-proteoglycan 3-β-glucuronosyltransferase EC 2.4.1.226 269077-98-7 Inquiry
EXWM-2454 N-acetylglucosaminyl-proteoglycan 4-β-glucuronosyltransferase EC 2.4.1.225 145539-84-0 Inquiry
EXWM-2453 glucuronosyl-N-acetylglucosaminyl-proteoglycan 4-α-N-acetylglucosaminyltransferase EC 2.4.1.224 336193-98-7 Inquiry
EXWM-2452 glucuronyl-galactosyl-proteoglycan 4-α-N-acetylglucosaminyltransferase EC 2.4.1.223 179241-74-8 Inquiry
EXWM-2451 O-fucosylpeptide 3-β-N-acetylglucosaminyltransferase EC 2.4.1.222 299203-70-6 Inquiry
EXWM-2450 peptide-O-fucosyltransferase EC 2.4.1.221 9033-08-3 Inquiry
EXWM-2449 indoxyl-UDPG glucosyltransferase EC 2.4.1.220 258339-72-9 Inquiry
EXWM-2448 lactose synthase EC 2.4.1.22 9030-11-9 Inquiry
EXWM-2447 vomilenine glucosyltransferase EC 2.4.1.219 Inquiry
EXWM-2446 hydroquinone glucosyltransferase EC 2.4.1.218 Inquiry
EXWM-2445 mannosyl-3-phosphoglycerate synthase EC 2.4.1.217 393512-63-5 Inquiry
EXWM-2444 trehalose 6-phosphate phosphorylase EC 2.4.1.216 403512-51-6 Inquiry
EXWM-2443 cis-zeatin O-β-D-glucosyltransferase EC 2.4.1.215 123644-76-8 Inquiry
EXWM-2442 glycoprotein 3-α-L-fucosyltransferase EC 2.4.1.214 68247-53-0 Inquiry
EXWM-2441 glucosylglycerol-phosphate synthase EC 2.4.1.213 161515-13-5 Inquiry
EXWM-2440 hyaluronan synthase EC 2.4.1.212 39346-43-5 Inquiry
EXWM-2439 1,3-β-galactosyl-N-acetylhexosamine phosphorylase EC 2.4.1.211 224427-06-9 Inquiry
EXWM-2438 limonoid glucosyltransferase EC 2.4.1.210 195836-82-9 Inquiry
EXWM-2437 starch synthase (glycosyl-transferring) EC 2.4.1.21 9030-10-8, 37338-93-5 Inquiry
EXWM-2436 cis-p-coumarate glucosyltransferase EC 2.4.1.209 196887-88-4 Inquiry
EXWM-2435 diglucosyl diacylglycerol synthase (1,2-linking) EC 2.4.1.208 168680-19-1 Inquiry
EXWM-2434 xyloglucan:xyloglucosyl transferase EC 2.4.1.207 141588-40-1 Inquiry