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Journal articles on the topic 'Protein L'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 April 2022

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1

Hara, T., T. Tanaka, H. Kato, T. Nishioka, and J. Oda. "Site-directed mutagenesis of glutathione synthetase from Escherichia coli B: mapping of the -L-glutamyl-L-cysteine-binding site." Protein Engineering Design and Selection 8, no. 7 (1995): 711–16. http://dx.doi.org/10.1093/protein/8.7.711.

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2

Housden, N. G., S. Harrison, S. E. Roberts, et al. "Immunoglobulin-binding domains: Protein L from Peptostreptococcus magnus." Biochemical Society Transactions 31, no. 3 (2003): 716–18. http://dx.doi.org/10.1042/bst0310716.

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Protein L is a multidomain cell-wall protein isolated from Peptostreptococcus magnus. It belongs to a group of proteins that contain repeated domains that are able to bind to Igs without stimulating an immune response, the most characterized of this group being Protein A (Staphylococcus aureus) and Protein G (Streptococcus). Both of these proteins bind predominantly to the interface of CH2-CH3 heavy chains, while Protein L binds exclusively to the VL domain of the κ-chain. The function of these proteins in vivo is not clear but it is thought that they enable the bacteria to evade the host's im

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3

Patalakh, I. I. "L-ARGININE AND L-GLUTAMIC ACID INCREASE THE CONTENT OF PROTEIN C IN THE EARLY STAGES OF ISOLATION FROM DONOR PLASMA." Biotechnologia Acta 14, no. 3 (2021): 30–38. http://dx.doi.org/10.15407/biotech14.03.030.

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Current large-scale production of blood-derived pharmacological preparations is aimed at expanding the list of products and deeper extraction of target proteins especially at the pre-purification stage. In particular, this problem becomes critical for the isolation of proteins like protein C (PC), which is present in plasma in trace amounts. Aim. We aimed to improve the buffer composition to minimize the interaction of PC with other proteins and lipids that are inevitably present in the stock material. Methods. The content of protein C in plasma and its derivatives was assessed by the amidolyt

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4

Barreiro, Gabriela, Cristiano Ruch Werneck Guimarães, and Ricardo Bicca de Alencastro. "A molecular dynamics study of an L-type calcium channel model." Protein Engineering, Design and Selection 15, no. 2 (2002): 109–22. http://dx.doi.org/10.1093/protein/15.2.109.

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5

Sorenson, Jon M., and Teresa Head-Gordon. "Protein Engineering Study of Protein L by Simulation." Journal of Computational Biology 9, no. 1 (2002): 35–54. http://dx.doi.org/10.1089/10665270252833181.

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6

Toprak, Neşe Nuray, İsmail Yavaş, Ali Anıl Çenesiz, Necmettin Ceylan, and İbrahim Çiftci. "Effects of digestible amino acid based formulation of low protein broiler diets supplemented with valine, isoleucine and arginine on performance and protein efficiency." Czech Journal of Animal Science 66, No. 5 (2021): 168–78. http://dx.doi.org/10.17221/293/2020-cjas.

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The aim of the present study was to investigate the effect of digestible amino acid (DAA) based formulation strategy, and l-valine (l-Val), l-isoleucine (l-Ile) and l-arginine (l-Arg) supplementation to reduce the crude protein (CP) level of broiler diets on performance, carcass characteristics and protein efficiency ratio by comparing with the control diet formulated on total amino acid base. A total of 792 one-day-old Ross 308 broiler chicks were divided into 48 floor pens, with 24 pens containing 16 chicks and 24 pens containing 17 chicks. The experiment was organized in a completely random

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7

Zhang, Jing, Yongxiang Wang, Shuwen Fu, et al. "Role of Small Envelope Protein in Sustaining the Intracellular and Extracellular Levels of Hepatitis B Virus Large and Middle Envelope Proteins." Viruses 13, no. 4 (2021): 613. http://dx.doi.org/10.3390/v13040613.

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Hepatitis B virus (HBV) expresses co-terminal large (L), middle (M), and small (S) envelope proteins. S protein drives virion and subviral particle secretion, whereas L protein inhibits subviral particle secretion but coordinates virion morphogenesis. We previously found that preventing S protein expression from a subgenomic construct eliminated M protein. The present study further examined impact of S protein on L and M proteins. Mutations were introduced to subgenomic construct of genotype A or 1.1 mer replication construct of genotype A or D, and viral proteins were analyzed from transfecte

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8

Einberger, H., R. Mertz, P. H. Hofschneider, and W. J. Neubert. "Purification, renaturation, and reconstituted protein kinase activity of the Sendai virus large (L) protein: L protein phosphorylates the NP and P proteins in vitro." Journal of Virology 64, no. 9 (1990): 4274–80. http://dx.doi.org/10.1128/jvi.64.9.4274-4280.1990.

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9

Zell, Roland, Simone Seitz, Andreas Henke, Thomas Munder, and Peter Wutzler. "Linkage map of protein–protein interactions of Porcine teschovirus." Journal of General Virology 86, no. 10 (2005): 2763–68. http://dx.doi.org/10.1099/vir.0.81144-0.

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A yeast two-hybrid study was conducted to catalogue the protein–protein interactions of the Porcine teschovirus non-structural proteins. Five homodimer, three reciprocal heterodimer and four unidirectional heterodimer interactions were observed. While several interactions are similar to those described in previous studies using enteroviruses, such as homo- and heterodimeric interactions of the 2B, 3CD and 3D proteins, several were not found previously. Among these is the binding of the leader protein L to the proteinases 3C and 3CD. Unlike the poliovirus 3C, the teschovirus 3C proteinase dimer

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10

Szuromi, P. "Single-protein spectroscopy." Science 347, no. 6226 (2015): 1109–11. http://dx.doi.org/10.1126/science.347.6226.1109-l.

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11

Feil, I. K., J. Hendle, and D. Schomburg. "Modified substrate specificity of L-hydroxyisocaproate dehydrogenase derived from structure-based protein engineering." Protein Engineering Design and Selection 10, no. 3 (1997): 255–62. http://dx.doi.org/10.1093/protein/10.3.255.

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12

Debeche, Takoua, Christophe Bliard, Philippe Debeire та Michael J. O'Donohue. "Probing the catalytically essential residues of the α-l-arabinofuranosidase from Thermobacillus xylanilyticus". Protein Engineering, Design and Selection 15, № 1 (2002): 21–28. http://dx.doi.org/10.1093/protein/15.1.21.

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13

Bart, Olivia M., and Andrew J. Piefer. "Exploring Protein‐Protein Interactions for MS2‐L Lysis Activity." FASEB Journal 34, S1 (2020): 1. http://dx.doi.org/10.1096/fasebj.2020.34.s1.05436.

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14

Åkerström, B., and L. Björck. "Protein L: An Immunoglobulin Light Chain-binding Bacterial Protein." Journal of Biological Chemistry 264, no. 33 (1989): 19740–46. http://dx.doi.org/10.1016/s0021-9258(19)47174-3.

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15

Clemente, Alfonso, Javier Vioque, Raúl Sánchez-Vioque, Justo Pedroche, Juan Bautista, and Francisco Millán. "Protein quality of chickpea (Cicer arietinum L.) protein hydrolysates." Food Chemistry 67, no. 3 (1999): 269–74. http://dx.doi.org/10.1016/s0308-8146(99)00130-2.

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16

CYGAN-SZCZEGIELNIAK, Dorota, Karolina STASIAK, Bogdan JANICKI, Aleksandra Roslewska, and Magdalena STANEK. "Blood plasma proteins and protein fractions in roe deer Capreolus capreolus L." Journal of Central European Agriculture 16, no. 3 (2015): 289–98. http://dx.doi.org/10.5513/jcea01/16.3.1622.

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17

Gelfand, I., A. Kister, C. Kulikowski, and O. Stoyanov. "Geometric invariant core for the V(L) and V(H) domains of immunoglobulin molecules." Protein Engineering Design and Selection 11, no. 11 (1998): 1015–25. http://dx.doi.org/10.1093/protein/11.11.1015.

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18

Edge, M., C. Forder, J. Hennam, et al. "Engineered human carboxypeptidase B enzymes that hydrolyse hippuryl-L- glutamic acid: reversed-polarity mutants." Protein Engineering Design and Selection 11, no. 12 (1998): 1229–34. http://dx.doi.org/10.1093/protein/11.12.1229.

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19

Rutherford, Karen, and Valerie Daggett. "The V119I polymorphism in protein L-isoaspartate O-methyltransferase alters the substrate-binding interface." Protein Engineering, Design and Selection 22, no. 12 (2009): 713–21. http://dx.doi.org/10.1093/protein/gzp056.

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20

Skibniewska, K. A., J. Zakrzewski, J. Kłobukowski, et al. "Nutritional value of the protein of consumer carp Cyprinus carpio L." Czech Journal of Food Sciences 31, No. 4 (2013): 313–17. http://dx.doi.org/10.17221/337/2012-cjfs.

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The nutritional value of the protein of carp from breeding technologies currently employed in Poland (semi-extensive, low-intensive and high-intensive ones) was evaluated. The total protein content was from 16.9% to 18.6% and did not diverge from the content of this nutrient in other fish species. The protein of the studied carps was characterised by a high content of exogenous amino acids, considerably exceeding their amount compared to the standard protein, irrespective of the area of breeding or the production intensity level. The dominant amino acids were histidine, methionine, and cystein

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21

Rexin, Dr A. "Effect of Sporlac on Protein Content of Silkworm Bombyx Mori L." International journal of Emerging Trends in Science and Technology 03, no. 03 (2017): 4994–97. http://dx.doi.org/10.18535/ijetst/v4i3.02.

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22

Peterson, A. A. "Accumulation of recombinant fusion protein — secretory analog of Ag85B and ESAT6 Mycobacterium tuberculosis proteins – in transgenic Lemna minor L. Plants." Biotechnologia acta 8, no. 5 (2015): 38–48. http://dx.doi.org/10.15407/biotech8.05.039.

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23

Khattar, Sunil K., Abdul S. Yunus, and Siba K. Samal. "Mapping the domains on the phosphoprotein of bovine respiratory syncytial virus required for N–P and P–L interactions using a minigenome system." Journal of General Virology 82, no. 4 (2001): 775–79. http://dx.doi.org/10.1099/0022-1317-82-4-775.

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The interaction of bovine respiratory syncytial virus (BRSV) phosphoprotein (P) with nucleocapsid (N) and large polymerase (L) proteins was investigated using an intracellular BRSV–CAT minigenome replication system. Coimmunoprecipitation assays using P-specific antiserum revealed that the P protein can form complexes with N and L proteins. Deletion mutant analysis of the P protein was performed to identify the regions of P protein that interact with N and L proteins. The results indicate that two independent N-binding sites exist on the P protein: an internal region of 161–180 amino acids and

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24

Yang, Rui, Ruishuang Sun, Wenlong Zhu, et al. "Heterologous Expression and Purification of Hagfish Mucus Protein." Journal of Biobased Materials and Bioenergy 15, no. 1 (2021): 20–32. http://dx.doi.org/10.1166/jbmb.2021.2031.

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To realize the application and production of hagfish mucus protein, this experiment increased the protein expression and improved its purification method. According to codon preference, the hagfish mucus protein gene was optimized to increase the production of target protein. Then, the protein expression conditions of the host bacteria were optimized, and the IPTG concentration, induction time and supplementation amounts of glycine, threonine, and serine were evaluated in single-factor tests. On the basis of single-factor experiments, with the supplementation of glycine, threonine, and serine

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25

Allen, Stuart J., and J. John Holbrook. "Production of an activated form of Bacillus stearothermophilus L-2-hydroxyacid dehydrogenase by directed evolution." Protein Engineering, Design and Selection 13, no. 1 (2000): 5–7. http://dx.doi.org/10.1093/protein/13.1.5.

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26

Kallwass, Helmut K. W., Witold K. Surewicz, Wendy Parris, et al. "Single amino acid substitutions can further increase the stability of a thermophilic L-lactate dehydrogenase." "Protein Engineering, Design and Selection" 5, no. 8 (1992): 769–74. http://dx.doi.org/10.1093/protein/5.8.769.

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27

Hartmann-Stühler, Cora, та Reinhild Prange. "Hepatitis B Virus Large Envelope Protein Interacts with γ2-Adaptin, a Clathrin Adaptor-Related Protein". Journal of Virology 75, № 11 (2001): 5343–51. http://dx.doi.org/10.1128/jvi.75.11.5343-5351.2001.

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ABSTRACT For the outcome of a hepatitis B virus (HBV) infection, the viral L envelope protein with its pre-S domain performs pivotal functions by mediating attachment of HBV to liver cells, envelopment of viral capsids, release of (sub)viral particles, regulation of supercoiled DNA amplification, and transcriptional transactivation. To assess its multiple functions and host-protein assistance involved, we initiated a two-hybrid screen using the L-specific pre-S1 domain as bait. With this approach, we have identified γ2-adaptin, a putative member of the clathrin adaptor proteins responsible for

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28

Chenik, M., M. Schnell, K. K. Conzelmann, and D. Blondel. "Mapping the Interacting Domains between the Rabies Virus Polymerase and Phosphoprotein." Journal of Virology 72, no. 3 (1998): 1925–30. http://dx.doi.org/10.1128/jvi.72.3.1925-1930.1998.

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ABSTRACT The RNA polymerase of rabies virus consists of two subunits, the large (L) protein and the phosphoprotein (P), with 2,127 and 297 amino acids, respectively. When these proteins were coexpressed via the vaccinia virus-T7 RNA polymerase recombinant in mammalian cells, they formed a complex as detected by coimmunoprecipitation. Analysis of P and L deletion mutants was performed to identify the regions of both proteins involved in complex formation. The interaction of P with L was not disrupted by large deletions removing the carboxy-terminal half of the P protein. On the contrary, P prot

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29

Jeon, Seung-Woo, Jay Ronel Conejos, Jungeun Kim, et al. "Supplementing conjugated and non-conjugated L-methionine and acetate alters expression patterns of CSN2, proteins and metabolites related to protein synthesis in bovine mammary cells." Journal of Dairy Research 87, no. 1 (2020): 70–77. http://dx.doi.org/10.1017/s0022029919000979.

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AbstractThe experiments reported in this research paper aimed to determine the effect of supplementing different forms of L-methionine (L-Met) and acetate on protein synthesis in immortalized bovine mammary epithelial cell line (MAC-T cells). Treatments were Control, L-Met, conjugated L-Met and acetate (CMA), and non-conjugated L-Met and Acetate (NMA). Protein synthesis mechanism was determined by omics method. NMA group had the highest protein content in the media and CSN2 mRNA expression levels (P < 0.05). The number of upregulated and downregulated proteins observed were 39 and 77 in L-M

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30

Paul, Sophie, and Thomas Michiels. "Cardiovirus leader proteins are functionally interchangeable and have evolved to adapt to virus replication fitness." Journal of General Virology 87, no. 5 (2006): 1237–46. http://dx.doi.org/10.1099/vir.0.81642-0.

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The leader (L) proteins encoded by picornaviruses of the genus Cardiovirus [Theiler's murine encephalomyelitis virus (TMEV) and Encephalomyocarditis virus (EMCV)] are small proteins thought to exert important functions in virus–host interactions. The L protein of persistent TMEV strains was shown to be dispensable for virus replication in vitro, but crucial for long-term persistence of the virus in the central nervous system of the mouse. The phenotype of chimeric viruses generated by exchanging the L-coding regions was analysed and it was shown that the L proteins of neurovirulent and persist

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31

Sugano, Mitsuko, Tatsunori Seki, and Hiroki Nakae. "Myelin basic protein gene-related protein (MGRP)." Neuroscience Research Supplements 17 (January 1992): 139. http://dx.doi.org/10.1016/0921-8696(92)90913-l.

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32

Ahrens, Susan, Mahesh Venkatachalam, Anahita M. Mistry, Karen Lapsley, and Shridhar K. Sathe. "Almond (Prunus dulcis L.) Protein Quality." Plant Foods for Human Nutrition 60, no. 3 (2005): 123–28. http://dx.doi.org/10.1007/s11130-005-6840-2.

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33

Martsev, S. P., A. P. Vlasov, and P. Arosio. "Distinct stability of recombinant L and H subunits of human ferritin: calorimetric and ANS binding studies." Protein Engineering Design and Selection 11, no. 5 (1998): 377–81. http://dx.doi.org/10.1093/protein/11.5.377.

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34

Funk, Michael A. "Protein backbone, broken and mended." Science 359, no. 6377 (2018): 756.12–758. http://dx.doi.org/10.1126/science.359.6377.756-l.

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35

Hurtley, S. M. "Opening up Vps34 protein complexes." Science 350, no. 6257 (2015): 173–75. http://dx.doi.org/10.1126/science.350.6257.173-l.

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36

So, Kenny K. Y., and Robert W. Duncan. "Breeding Canola (Brassica napus L.) for Protein in Feed and Food." Plants 10, no. 10 (2021): 2220. http://dx.doi.org/10.3390/plants10102220.

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Interest in canola (Brassica napus L.). In response to this interest, scientists have been tasked with altering and optimizing the protein production chain to ensure canola proteins are safe for consumption and economical to produce. Specifically, the role of plant breeders in developing suitable varieties with the necessary protein profiles is crucial to this interdisciplinary endeavour. In this article, we aim to provide an overarching review of the canola protein chain from the perspective of a plant breeder, spanning from the genetic regulation of seed storage proteins in the crop to advan

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37

Sirtori, Cesare R., Michela Triolo, Raffaella Bosisio, et al. "Hypocholesterolaemic effects of lupin protein and pea protein/fibre combinations in moderately hypercholesterolaemic individuals." British Journal of Nutrition 107, no. 8 (2011): 1176–83. http://dx.doi.org/10.1017/s0007114511004120.

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The present study was aimed to evaluate the effect of plant proteins (lupin protein or pea protein) and their combinations with soluble fibres (oat fibre or apple pectin) on plasma total and LDL-cholesterol levels. A randomised, double-blind, parallel group design was followed: after a 4-week run-in period, participants were randomised into seven treatment groups, each consisting of twenty-five participants. Each group consumed two bars containing specific protein/fibre combinations: the reference group consumed casein+cellulose; the second and third groups consumed bars containing lupin or pe

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38

Sánchez, Ana B., and Juan C. de la Torre. "Genetic and Biochemical Evidence for an Oligomeric Structure of the Functional L Polymerase of the Prototypic Arenavirus Lymphocytic Choriomeningitis Virus." Journal of Virology 79, no. 11 (2005): 7262–68. http://dx.doi.org/10.1128/jvi.79.11.7262-7268.2005.

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ABSTRACT The arenavirus L protein has the characteristic sequence motifs conserved among the RNA-dependent RNA polymerase L proteins of negative-strand (NS) RNA viruses. Studies based on the use of reverse-genetics approaches have provided direct experimental evidence of the key role played by the arenavirus L protein in viral-RNA synthesis. Sequence alignment shows six conserved domains among L proteins of NS RNA viruses. The proposed polymerase module of L is located within its domain III, which contains highly conserved amino acids within motifs designated A and C. We have examined the role

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39

Mukherjee, Mandira, Mark T. Brown, Andrew G. McArthur, and Patricia J. Johnson. "Proteins of the Glycine Decarboxylase Complex in the Hydrogenosome of Trichomonas vaginalis." Eukaryotic Cell 5, no. 12 (2006): 2062–71. http://dx.doi.org/10.1128/ec.00205-06.

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ABSTRACT Trichomonas vaginalis is a unicellular eukaryote that lacks mitochondria and contains a specialized organelle, the hydrogenosome, involved in carbohydrate metabolism and iron-sulfur cluster assembly. We report the identification of two glycine cleavage H proteins and a dihydrolipoamide dehydrogenase (L protein) of the glycine decarboxylase complex in T. vaginalis with predicted N-terminal hydrogenosomal presequences. Immunofluorescence analyses reveal that both H and L proteins are localized in hydrogenosomes, providing the first evidence for amino acid metabolism in this organelle. A

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40

Bronský, Jiří, Michal Karpíšek, Eva Bronská, et al. "Adiponectin, Adipocyte Fatty Acid Binding Protein, and Epidermal Fatty Acid Binding Protein: Proteins Newly Identified in Human Breast Milk." Clinical Chemistry 52, no. 9 (2006): 1763–70. http://dx.doi.org/10.1373/clinchem.2005.063032.

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Abstract Background: Breastfeeding may protect children from developing metabolic syndrome and other diseases later in life. We investigated novel proteins in human breast milk that might play a role in this process. Methods: We used ELISA to measure adiponectin, adipocyte and epidermal fatty acid binding proteins (AFABP, EFABP), and leptin concentrations in human breast milk obtained from 59 mothers 48 h after initiation of lactation. Using a questionnaire and medical records, we collected information about the mothers and newborns. Results: Mean (SE) adiponectin concentrations in breast milk

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41

Åkerström, Bo, and Lars Björck. "Bacterial Surface Protein L Binds and Inactivates Neutrophil Proteins S100A8/A9." Journal of Immunology 183, no. 7 (2009): 4583–92. http://dx.doi.org/10.4049/jimmunol.0901487.

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42

Wang, Shuqiang, Yang Lu, Quan Hong, et al. "Protein Array-Based Detection of Proteins in Kidney Tissues from Patients with Membranous Nephropathy." BioMed Research International 2017 (2017): 1–9. http://dx.doi.org/10.1155/2017/7843584.

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Membranous nephropathy (MN) is an autoimmune inflammatory disease in which proteins related with plenty of biological processes play an important role. However, the role of these proteins in the pathogenesis of MN is still unclear. This study aimed to screen differential proteins in kidney tissue samples from MN patients by using protein arrays and determine the pathways involved in the pathogenesis of MN. This study first tested a quantitative protein array (QAH-INF-3) and two semiquantitative protein arrays (L-493 and L-507) with normal renal tissue and identified L-493 as the most appropria

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43

Pepper, L. R., R. Parthasarathy, G. P. Robbins, N. N. Dang, D. A. Hammer, and E. T. Boder. "Isolation of L I domain mutants mediating firm cell adhesion using a novel flow-based sorting method." Protein Engineering Design and Selection 26, no. 8 (2013): 515–21. http://dx.doi.org/10.1093/protein/gzt028.

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44

Moroz, Yurii S., Wolfgang Binder, Patrik Nygren, Gregory A. Caputo та Ivan V. Korendovych. "Painting proteins blue: β-(1-azulenyl)-l-alanine as a probe for studying protein–protein interactions". Chem. Commun. 49, № 5 (2013): 490–92. http://dx.doi.org/10.1039/c2cc37550h.

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45

Piñol-Roma, S., M. S. Swanson, J. G. Gall, and G. Dreyfuss. "A novel heterogeneous nuclear RNP protein with a unique distribution on nascent transcripts." Journal of Cell Biology 109, no. 6 (1989): 2575–87. http://dx.doi.org/10.1083/jcb.109.6.2575.

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Immediately after the initiation of transcription in eukaryotes, nascent RNA polymerase II transcripts are bound by nuclear proteins resulting in the formation of heterogeneous nuclear ribonucleoprotein (hnRNP) complexes. hnRNP complexes from HeLa cell nuclei contain greater than 20 major proteins in the molecular mass range of 34,000-120,000 D. Among these are the previously described A, B, and C groups of proteins (34,000-43,000 D) and several larger, and as yet uncharacterized, proteins. Here we describe the isolation and characterization of a novel hnRNP protein termed the L protein (64-68

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46

Somasekharan, Deepthi, and Dr K. M. Khaleel Dr. K. M. Khaleel. "Radiation induced enhancement of protein content in Soybean (Glycine max L. Merr)." International Journal of Scientific Research 2, no. 12 (2012): 49–50. http://dx.doi.org/10.15373/22778179/dec2013/16.

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47

Conejos, Jay Ronel V., Jalil Ghassemi Nejad, Jung-Eun Kim, Jun-Ok Moon, Jae-Sung Lee, and Hong-Gu Lee. "Supplementing with L-Tryptophan Increases Medium Protein and Alters Expression of Genes and Proteins Involved in Milk Protein Synthesis and Energy Metabolism in Bovine Mammary Cells." International Journal of Molecular Sciences 22, no. 5 (2021): 2751. http://dx.doi.org/10.3390/ijms22052751.

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The objective of this study was to investigate the effects of supplementing with L-tryptophan (L-Trp) on milk protein synthesis using an immortalized bovine mammary epithelial (MAC-T) cell line. Cells were treated with 0, 0.3, 0.6, 0.9, 1.2, and 1.5 mM of supplemental L-Trp, and the most efficient time for protein synthesis was determined by measuring cell, medium, and total protein at 0, 24, 48, 72, and 96 h. Time and dose tests showed that the 48 h incubation time and a 0.9 mM dose of L-Trp were the optimal values. The mechanism of milk protein synthesis was elucidated through proteomic anal

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48

Gdala, J., A. J. M. Jansman, P. van Leeuwen, J. Huisman, and M. W. A. Verstegen. "Lupins (L. luteus, L. albus, L. angustifolius) as a protein source for young pigs." Animal Feed Science and Technology 62, no. 2-4 (1996): 239–49. http://dx.doi.org/10.1016/s0377-8401(96)00992-3.

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49

Cheng, Yunhe, Lili Cheng, Qingchang Cao, et al. "Heterologous Expression of SvMBD5 from Salix viminalis L. Promotes Flowering in Arabidopsis thaliana L." Genes 11, no. 3 (2020): 285. http://dx.doi.org/10.3390/genes11030285.

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Methyl-CpG-binding domain (MBD) proteins have diverse molecular and biological functions in plants. Most studies of MBD proteins in plants have focused on the model plant Arabidopsis thaliana L. Here we cloned SvMBD5 from the willow Salix viminalis L. by reverse transcription-polymerase chain reaction (RT-PCR) and analyzed the structure of SvMBD5 and its evolutionary relationships with proteins in other species. The coding sequence of SvMBD5 is 645 bp long, encoding a 214 amino acid protein with a methyl-CpG-binding domain. SvMBD5 belongs to the same subfamily as AtMBD5 and AtMBD6 from Arabido

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Shi, Xiaohong, and Richard M. Elliott. "Generation and analysis of recombinant Bunyamwera orthobunyaviruses expressing V5 epitope-tagged L proteins." Journal of General Virology 90, no. 2 (2009): 297–306. http://dx.doi.org/10.1099/vir.0.007567-0.

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Abstract:

The L protein of Bunyamwera virus (BUNV; family Bunyaviridae) is an RNA-dependent RNA polymerase, 2238 aa in length, that catalyses transcription and replication of the negative-sense, tripartite RNA genome. To learn more about the molecular interactions of the L protein and to monitor its intracellular distribution we inserted a 14 aa V5 epitope derived from parainfluenza virus type 5, against which high-affinity antibodies are available, into different regions of the protein. Insertion of the epitope at positions 1935 or 2046 resulted in recombinant L proteins that retained functionality in

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