Fluorescent-Labeled Peptides
Fluorescent-Labeled Peptides
Fluorescent-labeled peptides are a class of bioactive peptides covalently conjugated with fluorescent moieties, enabling molecular-level visualization with high sensitivity, safety, and cost-effectiveness. The principle relies on the fact that fluorophores contain conjugated double-bond systems that, upon excitation by ultraviolet or violet-blue light, return from an excited state to the ground state while releasing photons, thereby generating detectable fluorescence signals.
1. Key Features and Advantages
High sensitivity: Capable of detecting molecules at very low concentrations for precise imaging.
Non-radioactive and safe: No radioactive contamination, ensuring safe experimental operations.
Cost-effective: More economical compared with radioactive labeling or advanced imaging technologies.
2.Selection of Fluorophores
In vitro studies: Fluorophores with emission wavelengths of 400–600 nm (e.g., AMC, FITC, TAMRA) are widely applied in cell-based or protein-based assays.
In vivo imaging: Fluorophores with emission wavelengths of 650–900 nm (e.g., ICG, Cy5.5, Nile Blue) provide strong tissue penetration and low background interference.
3. Applications of Fluorescent-Labeled Peptides
3.1 Peptide Synthesis and Labeling
Fluorophores are typically conjugated to the N-terminus or C-terminus of peptides via covalent bonds to preserve biological activity. For long-chain peptides, FRET (Förster Resonance Energy Transfer) donor–acceptor pairs can be introduced within the sequence to investigate protein–protein interactions.
3.2 Application of FRET Technology
FRET technology enables the study of intermolecular interactions through non-radiative energy transfer between donor and acceptor fluorophores. FRET efficiency is inversely proportional to the sixth power of the donor–acceptor distance, allowing precise monitoring of protein–protein interactions, enzymatic activity, and molecular dynamics.
3.3 In vitro and In vivo Imaging
In vitro imaging: Confocal and fluorescence microscopy with labeled peptides allows efficient investigation of intracellular molecular targets and biological processes.
In vivo imaging: Fluorescent-labeled peptides enable real-time imaging in living organisms, applied in angiography, tumor imaging, and other biomedical fields, supporting precision medicine and personalized therapeutic strategies.
4.Common Fluorescent Modifications for Peptides
Name | Excitation (nm) | Emission (nm) | Emission Color |
7-Methoxycoumarin-4-acetic acid | 328 | 393 | Blue |
FITC-Ahx | 494 | 521 | Green |
FAM | 495 | 520 | Green |
Cy3 | 555 | 570 | Yellow |
5-Carboxytetramethylrhodamine (TMR) | 542 | 568 | Orange |
Cy5 | 646 | 662 | Red |
Cy5.5 | 673 | 707 | Near-infrared |
Cy7 | 750 | 773 | Near-infrared |
5.Representative FRET Pairs
Donor | Ex (nm) | Em (nm) | Acceptor | Ex (nm) | Em (nm) |
Cy2 | 490 | 510 | Cy3 | 555 | 570 |
FITC | 494 | 521 | TRITC | 557 | 576 |
FAM | 495 | 520 | Cy3 | 555 | 570 |
FAM | 495 | 520 | Texas Red | 589 | 615 |
FAM | 495 | 520 | Cy5 | 646 | 662 |
Cy3 | 555 | 570 | Cy5 | 646 | 662 |
EDANS | 335 | 493 | DABCYL | 453 | - |
Glu(EDANS)-NH2 | 335 | 493 | DABCYL | 453 | - |
MCA | 328 | 393 | DNP | 348 | - |
Abz | 330 | 420 | DNP | 348 | - |
Abz | 330 | 420 | Tyr (3-NO2) | 360 | - |
6. Quotation and Ordering
Detailed workflows, technical specifications, and quotation information for customized fluorescent peptide services are available on our official website. Professional technical support will be provided to meet your research needs.
Aladdin: https://www.aladdinsci.com/
