Direct comparison of KATUSHKA far-red fluorescent protein variants with luciferase bioluminescence in xenograft mouse models of epithelial tumor studies
نویسندگان
چکیده
Background. Research in oncology assumes establishment and usage of xenograft animal models, meeting the requirements humanity rationality. Although praised as promising field research, preclinical studies low-molecular-weight inhibitors, antitumor monoclonal antibodies, vaccines, cellular therapy products, CAR-T cells entail continuous control tumor growth dynamics. Luciferase detection bioluminescence requires injection a reporter substrate. However, injections not only are laborious, time-consuming expensive, but also stressful for animals. Thus, vast variety new visualization methods is employed, including proteins far-red spectrum. Objective. The study aimed to compare efficiency dynamics mice models cervical cancer, applying commercially available line fluorescent red protein derivatives Katushka clade Renilla luciferase, that commonly used vivo . Design methods. Xenograft were derived injecting modified HeLa cell line, expresses proteins: Katushka, Katushka2S, TurboRFP, TurboFP650 enzyme. Results. Spectral properties emission wavelength Katushka2S outlines these markers within RFP lineage outstanding instrument visualization. Conclusion. Detection reporters can be considered credible alternative luciferase experimental on part immunotherapy research.
منابع مشابه
Optimized and far-red-emitting variants of fluorescent protein eqFP611.
Fluorescent proteins (FPs) emitting in the far-red region of the spectrum are highly advantageous for whole-body imaging applications because scattering and absorption of long-wavelength light is markedly reduced in tissue. We characterized variants of the red fluorescent protein eqFP611 with bright fluorescence emission shifted up to 639 nm. The additional red shift is caused by a trans-cis is...
متن کاملCrystallographic study of red fluorescent protein eqFP578 and its far-red variant Katushka reveals opposite pH-induced isomerization of chromophore.
The wild type red fluorescent protein eqFP578 (from sea anemone Entacmaea quadricolor, λ(ex) = 552 nm, λ(em) = 578 nm) and its bright far-red fluorescent variant Katushka (λ(ex) = 588 nm, λ(em) = 635 nm) are characterized by the pronounced pH dependence of their fluorescence. The crystal structures of eqFP578f (eqFP578 with two point mutations improving the protein folding) and Katushka have be...
متن کاملFar-red fluorescent tag for protein labelling.
Practical applications of green fluorescent protein ('GFP')-like fluorescent proteins (FPs) from species of the class Anthozoa (sea anemones, corals and sea pens) are strongly restricted owing to their oligomeric nature. Here we suggest a strategy to overcome this problem by the use of two covalently linked identical red FPs as non-oligomerizing fusion tags. We have applied this approach to the...
متن کاملcomparison of catalytic activity of heteropoly compounds in the synthesis of bis(indolyl)alkanes.
heteropoly acids (hpa) and their salts have advantages as catalysts which make them both economically and environmentally attractive, strong br?nsted acidity, exhibiting fast reversible multi-electron redox transformations under rather mild conditions, very high solubility in polar solvents, fairly high thermal stability in the solid states, and efficient oxidizing ability, so that they are imp...
15 صفحه اولEstablishment of Green Fluorescent Protein and Firefly Luciferase Expressing Mouse Primary Macrophages for In Vivo Bioluminescence Imaging
Macrophages play a key role in tissue homeostasis as well as in a range of pathological conditions including atherosclerosis, cancer, and autoimmunity. Many aspects of their in vivo behavior are, however, poorly understood. Bioluminescence imaging (BLI) with green fluorescent protein (GFP) and firefly luciferase (FLUC) labelled autologous reporter macrophages could potentially offer a powerful ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: ?????????????? ????????
سال: 2023
ISSN: ['2782-389X', '2409-5516']
DOI: https://doi.org/10.18705/2311-4495-2022-9-6-59-70