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Recent studies suggest that seaweed extracts are a significant source of bioactive compounds comparable to the dietary phytochemicals such as onion and tea extracts. The exploration of natural antioxidants that attenuate oxidative damage is important for developing strategies to treat obesity‐related pathologies. The objective of this study was to screen the effects of seaweed extracts of 49 species on adipocyte differentiation and reactive oxygen species (ROS) production during the adipogenesis in 3T3‐L1 adipocytes, and to investigate their total phenol contents and 2,2‐diphenyl‐1‐picrylhydrazyl (DPPH) radical scavenging activities. Our results show that high total phenol contents were observed in the extracts of Ecklonia cava (see Table 1 for taxonomic authors) (681.1 ± 16.0 μg gallic acid equivalents [GAE] · g?1), Dictyopteris undulata (641.3 ± 70.7 μg GAE · g?1), and Laurencia intermedia (560.9 ± 48.1 μg GAE · g?1). In addition, DPPH radical scavenging activities were markedly higher in Sargassum macrocarpum (60.2%), Polysiphonia morrowii (55.0%), and Ishige okamurae (52.9%) than those of other seaweed extracts (P < 0.05). Moreover, treatment with several seaweed extracts including D. undulata, Sargassum micracanthum, Chondrus ocellatus, Gelidium amansii, Gracilaria verrucosa, and Grateloupia lanceolata significantly inhibited adipocyte differentiation and ROS production during differentiation of 3T3‐L1 preadipocytes. Furthermore, the production of ROS was positively correlated with lipid accumulation (R2 = 0.8149). According to these preliminary results, some of the seaweed extracts can inhibit ROS generation, which may protect against oxidative stress that is linked to obesity. Further studies are required to determine the molecular mechanism between the verified seaweeds and ROS, and the resulting effects on obesity.
Table 1. List of Korean seaweed extracts of 49 species evaluated in this experiment.
Type No. Scientific name Collection time TP1 (μg GAE · g?1)
Brown macroalgae SE‐1 Chondracanthus tenellus (Harv.) Hommers. April 27, 2006 112.8 ± 15.1lm
SE‐2 Colpomenia sinusa (F. C. Mertens ex Roth) Derbes et Solier in Castagne May 11, 2006 44.0 ± 4.1opqrs
SE‐3 Dictyopteris divaricata (Okamura) Okamura April 6, 2006 41.5 ± 5.6pqrs
SE‐4 Dictyopteris pacifica (Yendo) I. K. Hwang, H.‐S. Kim et W. J. Lee April 27, 2006 80.9 ± 8.3mno
SE‐5 Dictyopteris prolifera (Okamura) Okamura November 26, 2007 48.4 ± 3.0nopqrs
SE‐6 Dictyopteris undulata Holmes July 28, 2007 641.3 ± 70.7b
SE‐7 Dictyota asiatica I. K. Hwang April 6, 2006 52.9 ± 7.6nonopqr
SE‐8 Ecklonia cava Kjellm. October 22, 2006 681.1 ± 16.0a
SE‐9 Ecklonia stolonifera Okamura November 26, 2007 36.5 ± 3.4pqrs
SE‐10 Endarachne binghamiae J. Agardh March 10, 2006 50.4 ± 2.6nopqrs
SE‐11 Hizikia fusiformis (Harv.) Okamura July 23, 2006 16.4 ± 1.2rs
SE‐12 Hydroclathrus clathratus (C. Agardh) M. Howe May 11, 2006 18.1 ± 0.9rs
SE‐13 Ishige okamurae Yendo May 26, 2006 237.4 ± 1.6h
SE‐14 Lethesia difformis (L.) Aresch. May 11, 2006 11.2 ± 1.9s
SE‐15 Myelophycus simplex (Harv.) Papenf. April 27, 2006 39.5 ± 3.2pqrs
SE‐16 Padina arborescens Holmes July 29, 2007 172.9 ± 23.1ij
SE‐17 Sargassum fulvellum (Turner) C. Agardh April 27, 2006 119.1 ± 5.6kl
SE‐18 Sargassum micracanthum (Kütz.) Endl. December 21, 2006 468.0 ± 22.7e
SE‐19 Sargassum patens C. Agardh January 21, 2007 41.5 ± 5.7pqrs
SE‐20 Sargassum confusum C. Agardh f. validum Yendo March 8, 2008 110.9 ± 3.5lm
SE‐21 Sargassum horneri (Turner) C. Agardh March 1, 2006 84.8 ± 9.4lmn
SE‐22 Sargassum macrocarpum C. Agardh January 21, 2007 353.9 ± 59.1g
SE‐23 Sargassum muticum (Yendo) Fensolt January 21, 2007 72.1 ± 14.9nop
SE‐24 Sargassum nipponium Yendo April 6, 2006 54.0 ± 3.5nopqr
SE‐25 Sargassum sagamianum Yendo March 8, 2008 41.0 ± 6.7pqrs
SE‐26 Sargassum thunbergii (Mertens ex Roth) Kuntze July 23, 2006 27.7 ± 0.8qrs
SE‐27 Scytosiphon gracilis Kogame May 26, 2006 30.2 ± 5.6qrs
SE‐28 Scytosiphon lomentaria (Lyngb.) Link May 11, 2006 66.5 ± 8.9nopq
Red macroalgae SE‐29 Bonnemaisonia hamifera Har. April 27, 2006 44.1 ± 2.3opqrs
SE‐30 Callophyllis crispata Okamura May 11, 2006 37.6 ± 12.6pqrs
SE‐31 Chondria crassicaulis Harv. May 11, 2006 45.4 ± 4.4opqrs
SE‐32 Chondrus crispus Stackh. May 26, 2006 40.7 ± 8.0pqrs
SE‐33 Chondrus ocellatus Holmes May 11, 2006 47.2 ± 1.7nopqrs
SE‐34 Gelidium amansii (J. V. Lamour.) J. V. Lamour. April 27, 2006 525.3 ± 35.9d
SE‐35 Gloioperltis furcata (Postels et Rupr.) J. Agardh May 26, 2006 147.7 ± 6.4jk
SE‐36 Gloioperltis complanta (Harv.) Yamada May 26, 2006 58.2 ± 6.4nopq
SE‐37 Gracilaria verrucosa (Hudson) Papenf. March 6, 2008 55.1 ± 7.5nopqr
SE‐38 Grateloupia elliptica Holmes May 26, 2006 154.4 ± 12.9j
SE‐39 Grateloupia filicina (J. V. Lamour.) C. Agardh May 11, 2006 38.2 ± 2.2pqrs
SE‐40 Grateloupia lanceolata (Okamura) Kawag. July 23, 2006 32.7 ± 3.0pqrs
SE‐41 Laurencia intermedia J. V. Lamour. May 11, 2006 560.9 ± 48.1c
SE‐42 Laurencia intricata J. V. Lamour. April 27, 2006 35.4 ± 4.0pqrs
SE‐43 Laurencia okamurae Yamada May 11, 2006 193.2 ± 41.9i
SE‐44 Lomentaria hakodatensis Yendo April 27, 2006 165.2 ± 15.1ij
SE‐45 Polyopes affinis (Harv.) Kawag. et H.‐W. Wang May 26, 2006 42.9 ± 2.3opqrs
SE‐46 Polysiphonia morrowii Harv. May 11, 2006 392.4 ± 40.3f
SE‐47 Prionitis cornea (Okamura) E. Y. Dawson October 22, 2006 47.9 ± 3.6nopqrs
Green macroalgae SE‐48 Enteromorpha prolifera (O. F. Müll.) J. Agardh March 26, 2006 42.0 ± 5.3pqrs
SE‐49 Ulva pertusa Kjellm. April 27, 2006 48.3 ± 3.8nopqrs
  • GAE, gallic acid equivalents; SE, seaweed extracts.
  • 1TP, total phenol content is micrograms of total phenol contents per gram of seaweed extract based on gallic acid as standard. The values are means ± SD from three replications.
  • a–sMeans in the same column not sharing a common letter are significantly different (P < 0.05) by Duncan’s multiple test.

Citing Literature

Number of times cited according to CrossRef: 21

  • Kas?m Cemal Güven, Burak Coban, Osman Özdemir, Pharmacology of Marine Macroalgae, Encyclopedia of Marine Biotechnology, 10.1002/9781119143802, (585-615), (2020). Wiley Online Library
  • Giovanna Bermano, Teodora Stoyanova, Franck Hennequart, Cherry L. Wainwright, Seaweed-derived bioactives as potential energy regulators in obesity and type 2 diabetes, , 10.1016/bs.apha.2019.10.002, (2019). Crossref
  • Ana Rocío Múzquiz de la Garza, Mireya Tapia-Salazar, Maribel Maldonado-Muñiz, Julián de la Rosa-Millán, Janet Alejandra Gutiérrez-Uribe, Liliana Santos-Zea, Bertha Alicia Barba-Dávila, Denis Ricque-Marie, Lucía Elizabeth Cruz-Suárez, Nutraceutical Potential of Five Mexican Brown Seaweeds, BioMed Research International, 10.1155/2019/3795160, 2019 , (1-15), (2019). Crossref
  • M. Lynn Cornish, Alan T. Critchley, Ole G. Mouritsen, A role for dietary macroalgae in the amelioration of certain risk factors associated with cardiovascular disease, Phycologia, 10.2216/15-77.1, 54 , 6, (649-666), (2019). Crossref
  • Carolina Gonçalves-Fernández, Jorge Sineiro, Ramón Moreira, Oreste Gualillo, Extraction and characterization of phlorotannin-enriched fractions from the Atlantic seaweed Bifurcaria bifurcata and evaluation of their cytotoxic activity in murine cell line, Journal of Applied Phycology, 10.1007/s10811-018-1729-2, (2019). Crossref
  • Noelia Flórez‐Fernández, María P Casas, María Jesús González‐Muñoz, Herminia Domínguez, Microwave hydrogravity pretreatment of Sargassum muticum before solvent extraction of antioxidant and antiobesity compounds, Journal of Chemical Technology & Biotechnology, 10.1002/jctb.5771, 94 , 1, (256-264), (2018). Wiley Online Library
  • Yannick Lerat, M. L. Cornish, Alan T. Critchley, Stéphane La Barre, Stephen S. Bates, Applications of Algal Biomass in Global Food and Feed Markets: From Traditional Usage to the Potential for Functional Products, Blue Biotechnology, 10.1002/9783527801718, (143-189), (2018). Wiley Online Library
  • Gabriele Andressa Zatelli, Ana Cláudia Philippus, Miriam Falkenberg, An overview of odoriferous marine seaweeds of the Dictyopteris genus: insights into their chemical diversity, biological potential and ecological roles, Revista Brasileira de Farmacognosia, 10.1016/j.bjp.2018.01.005, 28 , 2, (243-260), (2018). Crossref
  • Cyr Abel Maranguy Ogandaga, Yeon Ju Na, Sang-Rae Lee, Young Sik Kim, Han Gil Choi, Ki Wan Nam, Wart-like spot formation on the fronds of Chondrus ocellatus (Gigartinales) by a brown alga, Mikrosyphar zosterae (Ectocarpales) in Korea, Journal of Applied Phycology, 10.1007/s10811-016-1028-8, 29 , 5, (2539-2546), (2017). Crossref
  • Fook Yee Chye, Birdie Scott Padam, Seah Young Ng, Innovation and Sustainable Utilization of Seaweeds as Health Foods, Sustainability Challenges in the Agrofood Sector, 10.1002/9781119072737, (390-434), (2017). Wiley Online Library
  • Gaurav Rajauria, Lynn Cornish, Francesco Ometto, Flower E. Msuya, Raffaella Villa, Identification and selection of algae for food, feed, and fuel applications, Seaweed Sustainability, 10.1016/B978-0-12-418697-2.00012-X, (315-345), (2015). Crossref
  • Jatinder Sangha, Owen Wally, Arjun Banskota, Roumiana Stefanova, Jeff Hafting, Alan Critchley, Balakrishnan Prithiviraj, A Cultivated Form of a Red Seaweed (Chondrus crispus), Suppresses β-Amyloid-Induced Paralysis in Caenorhabditis elegans, Marine Drugs, 10.3390/md13106407, 13 , 10, (6407-6424), (2015). Crossref
  • Jung-Ae Kim, Fatih Karadeniz, Byul-Nim Ahn, Myeong Sook Kwon, Ok-Ju Mun, Mihyang Kim, Sang-Hyeon Lee, Ki Hwan Yu, Yuck Yong Kim, Chang-Suk Kong, Sargassum sp. Attenuates Oxidative Stress and Suppresses Lipid Accumulation in vitro, Journal of Life Science, 10.5352/JLS.2014.24.3.274, 24 , 3, (274-283), (2014). Crossref
  • Georgia M. Hart, Tamara Ticktin, Dovi Kelman, Anthony D. Wright, Nicole Tabandera, Contemporary Gathering Practice and Antioxidant Benefit of Wild Seaweeds in Hawai’i, Economic Botany, 10.1007/s12231-014-9258-7, 68 , 1, (30-43), (2014). Crossref
  • Zahid Manzoor, Vivek Bhakta Mathema, Doobyeong Chae, Eun-Sook Yoo, Hee-Kyoung Kang, Jin-Won Hyun, Nam Ho Lee, Mi-Hee Ko, Young-Sang Koh, Extracts of the seaweed Sargassum macrocarpum inhibit the CpG-induced inflammatory response by attenuating the NF-κB pathway, Food Science and Biotechnology, 10.1007/s10068-014-0041-4, 23 , 1, (293-297), (2013). Crossref
  • Jatinder Singh Sangha, Di Fan, Arjun H. Banskota, Roumiana Stefanova, Wajahatullah Khan, Jeff Hafting, James Craigie, Alan T. Critchley, Balakrishnan Prithiviraj, Bioactive components of the edible strain of red alga, Chondrus crispus, enhance oxidative stress tolerance in Caenorhabditis elegans, Journal of Functional Foods, 10.1016/j.jff.2013.04.001, 5 , 3, (1180-1190), (2013). Crossref
  • Areum Daseul Kim, Mei Jing Piao, Yu Jae Hyun, Hee Kyoung Kang, In Soo Suh, Nam Ho Lee, Jin Won Hyun, Photo-protective properties of Lomentaria hakodatensis yendo against ultraviolet B radiation-induced keratinocyte damage, Biotechnology and Bioprocess Engineering, 10.1007/s12257-012-0336-3, 17 , 6, (1223-1231), (2013). Crossref
  • Min‐Jung Seo, Hyeon‐Son Choi, Ok‐Hwan Lee, Boo‐Yong Lee, Grateloupia lanceolata (Okamura) Kawaguchi, the Edible Red Seaweed, Inhibits Lipid Accumulation and Reactive Oxygen Species Production During Differentiation in 3T3‐L1 Cells, Phytotherapy Research, 10.1002/ptr.4765, 27 , 5, (655-663), (2012). Wiley Online Library
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Volume 47 , Issue 3 June 2011

Pages 548-556  相似文献   


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Nicola Nadeau 《Molecular ecology》2014,23(18):4441-4443
How common is hybridization between species and what effect does it have on the evolutionary process? Can hybridization generate new species and what indeed is a species? In this issue, Gompert et al. (2014) show how massive, genome‐scale data sets can be used to shed light on these questions. They focus on the Lycaeides butterflies, and in particular, several populations from the western USA, which have characteristics suggesting that they may contain hybrids of two or more different species (Gompert et al. 2006). They demonstrate that these populations do contain mosaic genomes made up of components from different parental species. However, this appears to have been largely driven by historical admixture, with more recent processes appearing to be isolating the populations from each other. Therefore, these populations are on their way to becoming distinct species (if they are not already) but have arisen following extensive hybridization between other distinct populations or species (Fig.  1 ).
Figure 1 Open in figure viewer PowerPoint There has been extensive historical admixture between Lycaeides species with some new species arising from hybrid populations. (Photo credits: Lauren Lucas, Chris Nice, and James Fordyce).
Their data set must be one of the largest outside of humans, with over one and half thousand butterflies genotyped at over 45 thousand variable nucleotide positions. It is this sheer amount of data that has allowed the researchers to distinguish between historical and more recent evolutionary and demographic processes. This is because it has allowed them to partition the data into common and rare genetic variants and perform separate analyses on these. Common genetic variants are likely to be older while rare variants are more likely to be due to recent mutations. Therefore, by splitting the genetic variation into these components, the researchers were able to show more admixture among common variants, while rare variants showed less admixture and clear separation of the populations. The extensive geographic sampling of individuals, including overlapping distributions of several of the putative species, also allowed the authors to rule out the possibility that the separation of the populations was simply due to geographical distance. The authors have developed a new programme for detecting population structure and admixture, which does the same job as STRUCTURE (Pritchard et al. 2000 ), identifying genetically distinct populations and admixture between these populations, but is designed to be used with next generation sequence data. They use the output of this model for another promising new method to distinguish between contemporary and historical admixtures. They fixed the number of source populations in the model at two and estimated the proportion of each individual's genome coming from these two populations. Therefore, an individual can either be purely population 1, or population 2 or some mixture of the two (they call this value q, the same parameter exists in STRUCTURE). They then compared this to the level of heterozygosity coming from the two source populations in the individual's genome. If an individual is an F1 hybrid of two source populations, then it would have a q of 0.5 and also be heterozygous at all loci that distinguish the parental populations. On the other hand, if it is a member of a stable hybrid lineage, it might also have a q of 0.5 but would not be expected to be heterozygous at these loci, because over time the population would become fixed for one or other of the source population states either by drift or selection (Fig.  2 ). This is indeed what they find in the hybrid populations. They tend to have intermediate q values, but the level of heterozygosity coming from the source populations (which they call Q12) was consistently lower than expected.
Figure 2 Open in figure viewer PowerPoint The Q‐matrix analysis used by Gompert et al. ( 2014 ) to distinguish between contemporary (hybrid swarm) and historical (stable hybrid lineage) admixture.
Overall, the results support several of the populations as being stable hybrid lineages. Nevertheless, the strictest definitions of hybrid species specify that the process of hybridization between the parental species must be instrumental in driving the reproductive isolation of the new species from both parental populations (Abbott et al. 2013 ). This is extremely hard to demonstrate conclusively because it requires us to first of all identify the isolating mechanisms that operated in the early evolution of the species and then to show that these were caused by the hybridization event itself. One advantage of the Lycaeides system is that the species appear to be in the early stages of divergence, so barriers to gene flow that are operating currently are likely to be those that are driving the species divergence. While there is some evidence that hybridization gave rise to traits that allowed the new populations to colonize new environments (Gompert et al. 2006 ; Lucas et al. 2008 ), there is clearly further work to be carried out in this direction. One of the rare examples of homoploid hybrid speciation (hybrid speciation without a change in chromosome number) where the reproductive isolation criterion has been demonstrated, comes from the Heliconius butterflies. In this case, hybridization of two species has been shown to give rise to a new colour pattern that instantly becomes reproductively isolated from the parental species due to mate preference for that pattern (Mavárez et al. 2006 ). However, while this has become a widely accepted example (Abbott et al. 2013 ), the naturally occurring ‘hybrid species’ in fact has derived most of its genome from one of the parental species, with largely just the colour pattern controlling locus coming from the other parent, a process that has been termed ‘hybrid trait speciation’ (Salazar et al. 2010 ). This distinction is an important one in terms of our understanding of the organization of biological diversity. While hybrid trait speciation will still largely fit the model of a neatly branching evolutionary tree, with perhaps only the region surrounding the single introgressed gene deviating from this model, hybrid species that end up with mosaic genomes, like Lycaeides, will not fit this model when considering the genome as a whole. This distinction also more broadly applies when comparing the patterns of divergence between Heliconius and Lycaeides. These two butterfly genera have been driving forward our understanding of the prevalence and importance of hybridization at the genomic level, but they reveal different ways in which hybridization can influence the organization of biological diversity. Recent work in Heliconius has shown that admixture is extensive and has been ongoing over a large portion of the evolutionary history of species (Martin et al. 2013 ; Nadeau et al. 2013 ). Nevertheless, this has not obscured the clear and robust pattern of a bifurcating evolutionary tree when considering the genome as a whole (Nadeau et al. 2013 ). In contrast in Lycaeides, the genome‐wide phylogeny clearly does not fit a bifurcating tree, resembling more of a messy shrub, with hybrid taxa falling at intermediate positions on the phylogeny (Gompert et al. 2014 ). The extent to which we need to rethink the way we describe and organize biological diversity will depend on the relative prevalence of these different outcomes of hybridization. We are likely to see many more of these types of large sequence data sets for ecologically interesting organisms. Gompert et al. ( 2014 ) show that these data need not only be a quantitative advance, but can also qualitatively change our understanding of the evolutionary history of these organisms. In particular, analysing common and rare genetic variants separately may provide information that would otherwise be missed. The emerging field of ‘speciation genomics’ (Seehausen et al. 2014 ) should follow this lead in developing new ways of making the most of the flood of genomic data that is being generated, but also improve methods for integrating this with field observations and experiments to identify the sources and targets of selection and divergence.

References

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  • Lucas LK , Fordyce JA , Nice CC (2008 ) Patterns of genitalic morphology around suture zones in North American Lycaeides (Lepidoptera: Lycaenidae): implications for taxonomy and historical biogeography . Annals of the Entomological Society of America, 101 , 172 – 180 . Crossref Web of Science® Google Scholar
  • Martin SH , Dasmahapatra KK , Nadeau NJ et al. (2013 ) Genome‐wide evidence for speciation with gene flow in Heliconius butterflies . Genome Research, 23 , 1817 – 1828 . Crossref CAS PubMed Web of Science® Google Scholar
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This article was written and figures prepared by N.N. except as specified in the text (photo credits).

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    Number of times cited according to CrossRef: 4

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    • Nicola J. Nadeau, Takeshi Kawakami, Population Genomics of Speciation and Admixture, , 10.1007/13836_2018_24, (2018). Crossref
    • Amanda Roe, Julian Dupuis, Felix Sperling, Molecular Dimensions of Insect Taxonomy in the Genomics Era, Insect Biodiversity, 10.1002/9781118945568, (547-573), (2017). Wiley Online Library

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    Highlights
    • •Identification of previously undetected chloroplast envelope proteins.
    • •Up to date manual annotation of genuine (or shared) envelope components.
    • •New hypotheses for localizations, functions, interactions among cell compartments.
    • •A new resource of significant value to the broader plant science community.
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    16.
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    Highlights
    • •Profiling antibody responses of patients with naturally acquired malaria immunity.
    • •High-density peptide arrays featuring linear epitopes.
    • •Epitope mapping of known and potential novel vaccine candidates.
    • •Novel immunogenic epitopes discovered, and known antibody target motifs confirmed.
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    17.
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    Highlights
    • •MHC-II-bound peptide repertoires from DO-sufficient and DO-deficient cells.
    • •Fewer unique peptides and core epitopes were presented in the absence of DO.
    • •Immunopeptidome differences appeared to result from reduced DM editing.
    • •DO-dependent self-epitopes elicited CD4 T cell responses in mice.
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    18.
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    Highlights
    • •Quantitative changes in global proteome and ubiquitinome in Huntington's disease.
    • •Differential ubiquitination of wild-type and mutant Htt in mice brain.
    • •Enriched pathways include vesicle transport and mRNA processing.
    • •Correlation between protein and diGly site fold changes.
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    19.
    20.
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    Highlights
    • •Chromobodies are stabilized by antigen binding in live cells.
    • •Monitoring changes of endogenous protein levels in living cells with chromobodies.
    • •Broadly applicable system to generate turnover-accelerated chromobodies.
    • •Quantification of time- and dose-dependent compound effects.
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