NHS-PEG4-COOH

Product#: LPA1113
$223.50
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NHS-PEG4-COOH

Cat. No.  LPA1113

Size        25 mg

Description

NHS-PEG4-COOH is a mono-functionalized PEG-based crosslinker that one end of diethylene glycol derivative is activated as NHS ester and can be used in a range of biological research fields. PEG crosslinkers are hydrophilic and does not penetrate cell membrane and beneficial to transfer their hydrophilic spacer to the crosslinked biomolecule thereby reducing the potential of aggregation and precipitation of the complex. NHS esters readily react with amine-modified oligonucleotides or amino groups of proteins or the amine terminus of nucleotides to form a chemically stable amide bond between dye and the biomolecule. Functionalized crosslinkers are one of well-known protein modification reagents that having a variety of applications in life science research and assay development.
 
Specifications
  • Reactive group: NHS ester
  • Molecular Weight: 491.44 g/mol
  • Solubility: Water, DMF, DMSO
  • Storage conditions: -20 ℃
 NHS ester
 
Quick link (Cat.#) Series Quick link (Cat.#) Series
LPA1111 NHS-PEG2-COOH LPA1211 NHS-PEG2B-COOH
LPA1112 NHS-PEG3-COOH LPA1212 NHS-PEG3B-COOH
LPA1113 NHS-PEG4-COOH LPA1213 NHS-PEG4B-COOH
LPA1114 NHS-PEG5-COOH LPA1214 NHS-PEG5B-COOH
LPA1115 NHS-PEG6-COOH LPA1215 NHS-PEG6B-COOH
LPA1116 NHS-PEG7-COOH LPA1216 NHS-PEG7B-COOH
LPA1117 NHS-PEG8-COOH LPA1217 NHS-PEG8B-COOH


Background

Biochemical Polymers & Labeling


The optimal labeling condition for biomolecules is to achieve an appropriate degree of conjugation ratio yet to retain the important functionality of the original biomolecules such as binding affinity, activatory or inhibitory activity, solubility and biological membrane permeability. The high-number of labeling often causes conjugated biomolecule to precipitate out of solution or to lose its functional properties, thus the degree of labeling should be determined from experimental optimization process. There are two major types of reactive dyes: amine-reactive dye and thiol-reactive dye. The primary target of amine-reactive probes at protein is lysine residue, and thiol residue is the main target for thiol-reactive probes. In mammalian proteins, the occurrence frequency of lysine residue is 7.2% and that of thiol is 3.3%.

      Amino-labeling is the widely utilized method to conjugate proteins, peptides, oligonucleotides and other biomolecules with dyes. Amine-reactive dyes might be used to prepare bioconjugates for fluorescent analog cytochemistry, immunochemistry, cell tracing, receptor labeling, FITC, etc. The primary target for amine-reactive probe is lysine residue, which has the fifth highest occurrence frequency of the 20 natural amino acids in mammalian proteins. A typical IgG antibody has about 90 lysine residues, and the maximum number of labeling will be around 30 residues with excess amount of reagent and prolonged incubation. However, maintaining functional properties requires the degree of labeling less than 10 dyes per antibody. BioActs provides three major classes (NHS, Sulfo-MHS and Vinylsulfone) of amine-reactive Flamma® Fluors dyes, and they can cover the entire spectral range from visible to NIR region. 

      Thiol-reactive dyes are mainly used for labeling proteins for the observation of conformational change, multi-subunit complexes assembly and ligand-binding processes. In proteins and peptides, the primary targets of thiol-reactive probes are cysteine residues. Unlike amine-labeling, the low abundance of cysteine residues enable to achieve saturated labeling without risk of conjugated protein precipitation and fluorescence self-quenching interactions. Thiols play a principal role in maintaining the appropriate oxidation–reduction state of proteins, cells and organisms, and they are easily oxidized to form disulfides. Thiols can also be generated by the reduction of cysteine disulfides with reducing agents such as dithiothreitol (DTT), 2-mercaptoethanol or tris-(2-carboxyethyl)phosphine (TCEP). However, the reducing process may cause to disrupt the tertiary structure of protein. Maleimide is a well-known reactive group that can specially label thiol of cysteine residue without interacting with amino functionality. In labeling process, thiol is added to the double bond of maleimide via 1,4-addition pathway to form thioether linkage. Maleimides apparently do not react with methionine, histidine or tyrosine, but they also react with amines in the strong basic environment. BioActs offers Flamma® Fluors maleimide series as thiol-reactive fluorescence dyes. 

      Click chemistry is a typical type of bioorthogonal reactions, which the reaction occurs inside of living systems yet without interfering with native biochemical processes. The most widely utilized click chemistry is 1,3-dipolar cycloaddition between an azide and an alkyne to produce 1,4-disubstituted 1,2,3-triazole. The triazole ring is stable under hydrolysis, oxidation or reduction, and it survives ionization process in mass spectrometry (MS) analysis. There are two types of 1,3-dipolar cycloaddition methods: copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) and strain-promoted azide-alkyne cycloaddition (SPAAC). BioActs offers Flamma® Fluors Alkyne dyes for CuAAC, Flamma® Fluors ADIBO products for SPAAC and Flamma® Fluors Azide dyes for both CuAAC and SPAAC.


Citation & Reference

1. Marina V. Backer. Vascular endothelial growth factor selectively targets boronated dendrimers to tumor vasculature. Mol Cancer Ther 4.9 (2005): 1423-9.

2. Zhenhui Chen. Spatial and Dynamic Interactions between Phospholamban and the Canine Cardiac Ca2 Pump Revealed with Use of Heterobifunctional Cross-linking Agents. J Biol Chem 278.48 (2003): 48348-56.

3. Katharina Deiss. Raf Kinase Inhibitor Protein (RKIP) Dimer Formation Controls Its Target Switch from Raf1 to G Protein-coupled Receptor Kinase (GRK) 2. J Biol Chem 287.28 (2012): 23407-17.

4. Nicole Schmitz. Displaying Fel d1 on virus-like particles prevents reactogenicity despite greatly enhanced immunogenicity: a novel therapy for cat allergy. J Exp Med 206.9 (2009): 1941-55.

5. Ariane L. Jansma. NMR Analysis of the Structure, Dynamics, and Unique Oligomerization Properties of the Chemokine CCL27. J Biol Chem 285.19 (2010): 14424-37.


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