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Analysis of surface carbohydrates of Trichobilharzia ocellata miracidia and sporocysts using lectin binding techniques.

Parasitology

Gerhardus MJ, Baggen JM, Van Der Knaap WP, Sminia T.
PMID: 23589931
Parasitology. 1991 Aug;103:51-9. doi: 10.1017/s003118200005928x.

Miracidia and in vitro-derived primary sporocysts of the avian schistosome Trichobilharzia ocellata were studied for the expression and the characteristics of glycoconjugate moieties comprising the surface coat. Using a panel of 9 peroxidase labelled lectins, several different lectin binding...

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Gerhardus MJ, Baggen JM, Van Der Knaap WP, et al. Analysis of surface carbohydrates of Trichobilharzia ocellata miracidia and sporocysts using lectin binding techniques. Parasitology. 1991;103:51-9doi: 10.1017/s003118200005928x.
Gerhardus, M. J., Baggen, J. M., Van Der Knaap, W. P., & Sminia, T. (1991). Analysis of surface carbohydrates of Trichobilharzia ocellata miracidia and sporocysts using lectin binding techniques. Parasitology, 10351-9. https://doi.org/10.1017/s003118200005928x
Gerhardus, M J, et al. "Analysis of surface carbohydrates of Trichobilharzia ocellata miracidia and sporocysts using lectin binding techniques." Parasitology vol. 103 (1991): 51-9. doi: https://doi.org/10.1017/s003118200005928x
Gerhardus MJ, Baggen JM, Van Der Knaap WP, Sminia T. Analysis of surface carbohydrates of Trichobilharzia ocellata miracidia and sporocysts using lectin binding techniques. Parasitology. 1991 Aug;103:51-9. doi: 10.1017/s003118200005928x. PMID: 23589931.
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Assessing acrosomal status of bovine sperm using fluoresceinated lectins.

Theriogenology

Cross NL, Watson SK.
PMID: 16727515
Theriogenology. 1994;42(1):89-98. doi: 10.1016/0093-691x(94)90665-6.

Binding of 12 lectins to bull sperm was analyzed to select a lectin that bound preferentially to the acrosomal region. Peanut agglutinin (PNA) and Pisum sativum agglutinin (PSA) were suitably specific for intracellular, acrosome-associated glycoconjugates. Peanut agglutinin exhibited almost...

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Cross NL, Watson SK. Assessing acrosomal status of bovine sperm using fluoresceinated lectins. Theriogenology. 1994;42(1):89-98doi: 10.1016/0093-691x(94)90665-6.
Cross, N. L., & Watson, S. K. (1994). Assessing acrosomal status of bovine sperm using fluoresceinated lectins. Theriogenology, 42(1), 89-98. https://doi.org/10.1016/0093-691x(94)90665-6
Cross, N L, and Watson, S K. "Assessing acrosomal status of bovine sperm using fluoresceinated lectins." Theriogenology vol. 42,1 (1994): 89-98. doi: https://doi.org/10.1016/0093-691x(94)90665-6
Cross NL, Watson SK. Assessing acrosomal status of bovine sperm using fluoresceinated lectins. Theriogenology. 1994;42(1):89-98. doi: 10.1016/0093-691x(94)90665-6. PMID: 16727515.
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The Glycoproteins of Plant Seeds : ANALYSIS BY TWO-DIMENSIONAL POLYACRYLAMIDE GEL ELECTROPHORESIS AND BY THEIR LECTIN-BINDING PROPERTIES.

Plant physiology

Basha SM, Roberts RM.
PMID: 16661796
Plant Physiol. 1981 May;67(5):936-9. doi: 10.1104/pp.67.5.936.

Protein from the jack bean, peanut, soybean and kidney bean seeds were extracted with a solution containing 9.3 molar urea, 5 millimolar K(2)CO(3), 0.5% dithiothreitol and 2% Nonidet P-40 and then subjected to two-dimensional gel electrophoresis. After electrophoresis, the...

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Basha SM, Roberts RM. The Glycoproteins of Plant Seeds : ANALYSIS BY TWO-DIMENSIONAL POLYACRYLAMIDE GEL ELECTROPHORESIS AND BY THEIR LECTIN-BINDING PROPERTIES. Plant Physiol. 1981;67(5):936-9doi: 10.1104/pp.67.5.936.
Basha, S. M., & Roberts, R. M. (1981). The Glycoproteins of Plant Seeds : ANALYSIS BY TWO-DIMENSIONAL POLYACRYLAMIDE GEL ELECTROPHORESIS AND BY THEIR LECTIN-BINDING PROPERTIES. Plant physiology, 67(5), 936-9. https://doi.org/10.1104/pp.67.5.936
Basha, S M, and Roberts, R M. "The Glycoproteins of Plant Seeds : ANALYSIS BY TWO-DIMENSIONAL POLYACRYLAMIDE GEL ELECTROPHORESIS AND BY THEIR LECTIN-BINDING PROPERTIES." Plant physiology vol. 67,5 (1981): 936-9. doi: https://doi.org/10.1104/pp.67.5.936
Basha SM, Roberts RM. The Glycoproteins of Plant Seeds : ANALYSIS BY TWO-DIMENSIONAL POLYACRYLAMIDE GEL ELECTROPHORESIS AND BY THEIR LECTIN-BINDING PROPERTIES. Plant Physiol. 1981 May;67(5):936-9. doi: 10.1104/pp.67.5.936. PMID: 16661796; PMCID: PMC425804.
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Fluorescent and Ferritin Labelling of Cuticle Surface Carbohydrates of Caenorhabditis elegans and Panagrellus redivivus.

Journal of nematology

Jansson HB, Jeyaprakash A, Coles GC, Marban-Mendoza N, Zuckerman BM.
PMID: 19294228
J Nematol. 1986 Oct;18(4):570-4.

Caenorhabditis elegans and Panagrellus redivivus were investigated for surface carbohydrates using fluorescent-labelled and ferritin-labelled lectins. Rhodamine-labelled Concanavalin A was specifically located in the cephalic region of both species. Rhodamine-labelled wheat germ agglutinin was located over the entire cuticle of...

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Jansson HB, Jeyaprakash A, Coles GC, et al. Fluorescent and Ferritin Labelling of Cuticle Surface Carbohydrates of Caenorhabditis elegans and Panagrellus redivivus. J Nematol. 1986;18(4):570-4
Jansson, H. B., Jeyaprakash, A., Coles, G. C., Marban-Mendoza, N., & Zuckerman, B. M. (1986). Fluorescent and Ferritin Labelling of Cuticle Surface Carbohydrates of Caenorhabditis elegans and Panagrellus redivivus. Journal of nematology, 18(4), 570-4.
Jansson, H B, et al. "Fluorescent and Ferritin Labelling of Cuticle Surface Carbohydrates of Caenorhabditis elegans and Panagrellus redivivus." Journal of nematology vol. 18,4 (1986): 570-4.
Jansson HB, Jeyaprakash A, Coles GC, Marban-Mendoza N, Zuckerman BM. Fluorescent and Ferritin Labelling of Cuticle Surface Carbohydrates of Caenorhabditis elegans and Panagrellus redivivus. J Nematol. 1986 Oct;18(4):570-4. PMID: 19294228; PMCID: PMC2618573.
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Lectin histochemistry to detect altered glycosylation in cells and tissues.

Methods in molecular medicine

Brooks SA, Hall DM.
PMID: 21340890
Methods Mol Med. 2001;57:49-65. doi: 10.1385/1-59259-136-1:49.

A lectin is "a protein or glycoprotein of non-immune origin, not an enzyme, that binds to carbohydrates and agglutinates cells" (1). Lectins are naturally occurring substances, most commonly derived from plant or sometimes invertebrate sources, that can be exploited...

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Brooks SA, Hall DM. Lectin histochemistry to detect altered glycosylation in cells and tissues. Methods Mol Med. 2001;57:49-65doi: 10.1385/1-59259-136-1:49.
Brooks, S. A., & Hall, D. M. (2001). Lectin histochemistry to detect altered glycosylation in cells and tissues. Methods in molecular medicine, 5749-65. https://doi.org/10.1385/1-59259-136-1:49
Brooks, S A, and Hall, D M. "Lectin histochemistry to detect altered glycosylation in cells and tissues." Methods in molecular medicine vol. 57 (2001): 49-65. doi: https://doi.org/10.1385/1-59259-136-1:49
Brooks SA, Hall DM. Lectin histochemistry to detect altered glycosylation in cells and tissues. Methods Mol Med. 2001;57:49-65. doi: 10.1385/1-59259-136-1:49. PMID: 21340890.
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Effects of L-carnitine and pentoxifylline on carbohydrate distribution of mouse testicular sperm membrane.

Iranian journal of medical sciences

Aliabadi E, Karimi F, Talaei-Khozani T.
PMID: 23825890
Iran J Med Sci. 2013 Jun;38(2):107-15.

BACKGROUND: The glycoconjugate content of sperms indicates their physiological and fertility properties. Lectin reactivity is indicative of intact, capacitated, and acrosome-reacted sperms. In the epididymis, sperms experience maturation, glycoconjugate modification, and simultaneously, higher L-carnitine (LC) concentrations. The aim of...

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Aliabadi E, Karimi F, Talaei-Khozani T. Effects of L-carnitine and pentoxifylline on carbohydrate distribution of mouse testicular sperm membrane. Iran J Med Sci. 2013;38(2):107-15
Aliabadi, E., Karimi, F., & Talaei-Khozani, T. (2013). Effects of L-carnitine and pentoxifylline on carbohydrate distribution of mouse testicular sperm membrane. Iranian journal of medical sciences, 38(2), 107-15.
Aliabadi, Elham, et al. "Effects of L-carnitine and pentoxifylline on carbohydrate distribution of mouse testicular sperm membrane." Iranian journal of medical sciences vol. 38,2 (2013): 107-15.
Aliabadi E, Karimi F, Talaei-Khozani T. Effects of L-carnitine and pentoxifylline on carbohydrate distribution of mouse testicular sperm membrane. Iran J Med Sci. 2013 Jun;38(2):107-15. PMID: 23825890; PMCID: PMC3700056.
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Successful delivery following intracytoplasmic sperm injection with calcium ionophore A23187 oocyte activation in a partially globozoospermic patient.

Reproductive medicine and biology

Kamiyama H, Shimizu T, Oki T, Asada T, Araki Y, Araki Y.
PMID: 29699121
Reprod Med Biol. 2012 Mar 16;11(3):159-164. doi: 10.1007/s12522-012-0123-z. eCollection 2012 Jul.

PURPOSE: To describe a successful pregnancy outcome following intracytoplasmic sperm injection (ICSI) with assisted oocyte activation (AOA) in a case of partial globozoospermia.METHODS: AOA was accomplished with calcium ionophore A23187. Sperm morphology was observed via light, fluorescent and electron...

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Kamiyama H, Shimizu T, Oki T, et al. Successful delivery following intracytoplasmic sperm injection with calcium ionophore A23187 oocyte activation in a partially globozoospermic patient. Reprod Med Biol. 2012;11(3):159-164doi: 10.1007/s12522-012-0123-z.
Kamiyama, H., Shimizu, T., Oki, T., Asada, T., Araki, Y., & Araki, Y. (2012). Successful delivery following intracytoplasmic sperm injection with calcium ionophore A23187 oocyte activation in a partially globozoospermic patient. Reproductive medicine and biology, 11(3), 159-164. https://doi.org/10.1007/s12522-012-0123-z
Kamiyama, Hiroshi, et al. "Successful delivery following intracytoplasmic sperm injection with calcium ionophore A23187 oocyte activation in a partially globozoospermic patient." Reproductive medicine and biology vol. 11,3 (2012): 159-164. doi: https://doi.org/10.1007/s12522-012-0123-z
Kamiyama H, Shimizu T, Oki T, Asada T, Araki Y, Araki Y. Successful delivery following intracytoplasmic sperm injection with calcium ionophore A23187 oocyte activation in a partially globozoospermic patient. Reprod Med Biol. 2012 Mar 16;11(3):159-164. doi: 10.1007/s12522-012-0123-z. eCollection 2012 Jul. PMID: 29699121; PMCID: PMC5907117.
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96-well plate format in conjunction with ultra-high-performance liquid chromatography coupled to orbitrap mass spectrometry for high-throughput screening protein binders from ginseng.

Journal of pharmaceutical and biomedical analysis

Shao S, Wang Y, Xie Z, Xu R, Wan X, Wang E, Wang Z, Liu S, Chen C, Yang H.
PMID: 34952293
J Pharm Biomed Anal. 2022 Feb 05;209:114498. doi: 10.1016/j.jpba.2021.114498. Epub 2021 Nov 29.

Conventional strategies for screening of protein binders cannot be used for complicated samples such as ligand libraries created by combinatorial chemistry or from natural product extracts. In the current study, we developed a novel method in a competitive binding...

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Shao S, Wang Y, Xie Z, et al. 96-well plate format in conjunction with ultra-high-performance liquid chromatography coupled to orbitrap mass spectrometry for high-throughput screening protein binders from ginseng. J Pharm Biomed Anal. 2021;209:114498doi: 10.1016/j.jpba.2021.114498.
Shao, S., Wang, Y., Xie, Z., Xu, R., Wan, X., Wang, E., Wang, Z., Liu, S., Chen, C., & Yang, H. (2022). 96-well plate format in conjunction with ultra-high-performance liquid chromatography coupled to orbitrap mass spectrometry for high-throughput screening protein binders from ginseng. Journal of pharmaceutical and biomedical analysis, 209114498. https://doi.org/10.1016/j.jpba.2021.114498
Shao, Simeng, et al. "96-well plate format in conjunction with ultra-high-performance liquid chromatography coupled to orbitrap mass spectrometry for high-throughput screening protein binders from ginseng." Journal of pharmaceutical and biomedical analysis vol. 209 (2022): 114498. doi: https://doi.org/10.1016/j.jpba.2021.114498
Shao S, Wang Y, Xie Z, Xu R, Wan X, Wang E, Wang Z, Liu S, Chen C, Yang H. 96-well plate format in conjunction with ultra-high-performance liquid chromatography coupled to orbitrap mass spectrometry for high-throughput screening protein binders from ginseng. J Pharm Biomed Anal. 2022 Feb 05;209:114498. doi: 10.1016/j.jpba.2021.114498. Epub 2021 Nov 29. PMID: 34952293.
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96-well plate format in conjunction with ultra-high-performance liquid chromatography coupled to orbitrap mass spectrometry for high-throughput screening protein binders from ginseng.

Journal of pharmaceutical and biomedical analysis

Shao S, Wang Y, Xie Z, Xu R, Wan X, Wang E, Wang Z, Liu S, Chen C, Yang H.
PMID: 34952293
J Pharm Biomed Anal. 2021 Nov 29;209:114498. doi: 10.1016/j.jpba.2021.114498. Epub 2021 Nov 29.

Conventional strategies for screening of protein binders cannot be used for complicated samples such as ligand libraries created by combinatorial chemistry or from natural product extracts. In the current study, we developed a novel method in a competitive binding...

Cite
Shao S, Wang Y, Xie Z, et al. 96-well plate format in conjunction with ultra-high-performance liquid chromatography coupled to orbitrap mass spectrometry for high-throughput screening protein binders from ginseng. J Pharm Biomed Anal. 2021;209:114498doi: 10.1016/j.jpba.2021.114498.
Shao, S., Wang, Y., Xie, Z., Xu, R., Wan, X., Wang, E., Wang, Z., Liu, S., Chen, C., & Yang, H. (2021). 96-well plate format in conjunction with ultra-high-performance liquid chromatography coupled to orbitrap mass spectrometry for high-throughput screening protein binders from ginseng. Journal of pharmaceutical and biomedical analysis, 209114498. https://doi.org/10.1016/j.jpba.2021.114498
Shao, Simeng, et al. "96-well plate format in conjunction with ultra-high-performance liquid chromatography coupled to orbitrap mass spectrometry for high-throughput screening protein binders from ginseng." Journal of pharmaceutical and biomedical analysis vol. 209 (2021): 114498. doi: https://doi.org/10.1016/j.jpba.2021.114498
Shao S, Wang Y, Xie Z, Xu R, Wan X, Wang E, Wang Z, Liu S, Chen C, Yang H. 96-well plate format in conjunction with ultra-high-performance liquid chromatography coupled to orbitrap mass spectrometry for high-throughput screening protein binders from ginseng. J Pharm Biomed Anal. 2021 Nov 29;209:114498. doi: 10.1016/j.jpba.2021.114498. Epub 2021 Nov 29. PMID: 34952293.
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Appearance of peanut agglutinin in the blood circulation after peanut ingestion promotes endothelial secretion of metastasis-promoting cytokines.

Carcinogenesis

Wang W, Sindrewicz-Goral P, Chen C, Duckworth CA, Pritchard DM, Rhodes JM, Yu LG.
PMID: 34223877
Carcinogenesis. 2021 Aug 19;42(8):1079-1088. doi: 10.1093/carcin/bgab059.

Peanut agglutinin (PNA) is a carbohydrate-binding protein in peanuts that accounts for ~0.15% peanut weight. PNA is highly resistant to cooking and digestion and is rapidly detectable in the blood after peanut consumption. Our previous studies have shown that...

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Wang W, Sindrewicz-Goral P, Chen C, et al. Appearance of peanut agglutinin in the blood circulation after peanut ingestion promotes endothelial secretion of metastasis-promoting cytokines. Carcinogenesis. 2021;42(8):1079-1088doi: 10.1093/carcin/bgab059.
Wang, W., Sindrewicz-Goral, P., Chen, C., Duckworth, C. A., Pritchard, D. M., Rhodes, J. M., & Yu, L. G. (2021). Appearance of peanut agglutinin in the blood circulation after peanut ingestion promotes endothelial secretion of metastasis-promoting cytokines. Carcinogenesis, 42(8), 1079-1088. https://doi.org/10.1093/carcin/bgab059
Wang, Weikun, et al. "Appearance of peanut agglutinin in the blood circulation after peanut ingestion promotes endothelial secretion of metastasis-promoting cytokines." Carcinogenesis vol. 42,8 (2021): 1079-1088. doi: https://doi.org/10.1093/carcin/bgab059
Wang W, Sindrewicz-Goral P, Chen C, Duckworth CA, Pritchard DM, Rhodes JM, Yu LG. Appearance of peanut agglutinin in the blood circulation after peanut ingestion promotes endothelial secretion of metastasis-promoting cytokines. Carcinogenesis. 2021 Aug 19;42(8):1079-1088. doi: 10.1093/carcin/bgab059. PMID: 34223877; PMCID: PMC8643467.
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96-well plate format in conjunction with ultra-high-performance liquid chromatography coupled to orbitrap mass spectrometry for high-throughput screening protein binders from ginseng.

Journal of pharmaceutical and biomedical analysis

Shao S, Wang Y, Xie Z, Xu R, Wan X, Wang E, Wang Z, Liu S, Chen C, Yang H.
PMID: 34952293
J Pharm Biomed Anal. 2021 Nov 29;209:114498. doi: 10.1016/j.jpba.2021.114498. Epub 2021 Nov 29.

Conventional strategies for screening of protein binders cannot be used for complicated samples such as ligand libraries created by combinatorial chemistry or from natural product extracts. In the current study, we developed a novel method in a competitive binding...

Cite
Shao S, Wang Y, Xie Z, et al. 96-well plate format in conjunction with ultra-high-performance liquid chromatography coupled to orbitrap mass spectrometry for high-throughput screening protein binders from ginseng. J Pharm Biomed Anal. 2021;209:114498doi: 10.1016/j.jpba.2021.114498.
Shao, S., Wang, Y., Xie, Z., Xu, R., Wan, X., Wang, E., Wang, Z., Liu, S., Chen, C., & Yang, H. (2021). 96-well plate format in conjunction with ultra-high-performance liquid chromatography coupled to orbitrap mass spectrometry for high-throughput screening protein binders from ginseng. Journal of pharmaceutical and biomedical analysis, 209114498. https://doi.org/10.1016/j.jpba.2021.114498
Shao, Simeng, et al. "96-well plate format in conjunction with ultra-high-performance liquid chromatography coupled to orbitrap mass spectrometry for high-throughput screening protein binders from ginseng." Journal of pharmaceutical and biomedical analysis vol. 209 (2021): 114498. doi: https://doi.org/10.1016/j.jpba.2021.114498
Shao S, Wang Y, Xie Z, Xu R, Wan X, Wang E, Wang Z, Liu S, Chen C, Yang H. 96-well plate format in conjunction with ultra-high-performance liquid chromatography coupled to orbitrap mass spectrometry for high-throughput screening protein binders from ginseng. J Pharm Biomed Anal. 2021 Nov 29;209:114498. doi: 10.1016/j.jpba.2021.114498. Epub 2021 Nov 29. PMID: 34952293.
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Sequential Changes in Aberrant Crypt Foci and Lectin Expression in the Early and Late Stages of DMH-Induced Colon Carcinogenesis in Rats.

Gut and liver

Won HS, Maeng LS, Chae HS, Kim HK, Cho YS, Kang JH, Jang HS, Ryu MR.
PMID: 22570753
Gut Liver. 2012 Apr;6(2):229-34. doi: 10.5009/gnl.2012.6.2.229. Epub 2012 Apr 17.

BACKGROUND/AIMS: The purpose of this study was to investigate the malignant potential of aberrant crypt foci (ACF) by measuring the multiplicity of crypts and lectin expression in the early and late stages of 1,2-dimethylhydrazine (DMH)-induced colon carcinogenesis.METHODS: Six-week-old Wistar...

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Won HS, Maeng LS, Chae HS, et al. Sequential Changes in Aberrant Crypt Foci and Lectin Expression in the Early and Late Stages of DMH-Induced Colon Carcinogenesis in Rats. Gut Liver. 2012;6(2):229-34doi: 10.5009/gnl.2012.6.2.229.
Won, H. S., Maeng, L. S., Chae, H. S., Kim, H. K., Cho, Y. S., Kang, J. H., Jang, H. S., & Ryu, M. R. (2012). Sequential Changes in Aberrant Crypt Foci and Lectin Expression in the Early and Late Stages of DMH-Induced Colon Carcinogenesis in Rats. Gut and liver, 6(2), 229-34. https://doi.org/10.5009/gnl.2012.6.2.229
Won, Hye Sung, et al. "Sequential Changes in Aberrant Crypt Foci and Lectin Expression in the Early and Late Stages of DMH-Induced Colon Carcinogenesis in Rats." Gut and liver vol. 6,2 (2012): 229-34. doi: https://doi.org/10.5009/gnl.2012.6.2.229
Won HS, Maeng LS, Chae HS, Kim HK, Cho YS, Kang JH, Jang HS, Ryu MR. Sequential Changes in Aberrant Crypt Foci and Lectin Expression in the Early and Late Stages of DMH-Induced Colon Carcinogenesis in Rats. Gut Liver. 2012 Apr;6(2):229-34. doi: 10.5009/gnl.2012.6.2.229. Epub 2012 Apr 17. PMID: 22570753; PMCID: PMC3343162.
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Showing 1 to 12 of 53 entries