Molecular structure of human-liver glycogen

PLoS ONE

Volumn 11, Issue 3, 2016, Pages

  Deng, Bin ^a   Sullivan, Mitchell A ^a,b,c   Chen, Cheng ^d   Li, Jialun ^a   Powell, Prudence O ^a,b   Hu, Zhenxia ^a   Gilbert, Robert G ^a,b  

^a HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^b UNIVERSITY OF QUEENSLAND   (Australia)

^c HOSPITAL FOR SICK CHILDREN   (Canada)

^d WUHAN GENERAL HOSPITAL OF GUANGZHOU COMMAND   (China)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOGEN; GLYCOGEN LIVER LEVEL;

ACID HYDROLYSIS; ADULT; AGED; ALPHA RADIATION; ANIMAL TISSUE; ARTICLE; CHEMICAL MODIFICATION; CHEMICAL STRUCTURE; CLINICAL ARTICLE; CONTROLLED STUDY; DIABETES MELLITUS; ELECTRON; FEMALE; GLYCOGEN LIVER LEVEL; GLYCOSIDATION; HUMAN; HUMAN TISSUE; HYDROLYSIS; IN VITRO STUDY; LINKAGE ANALYSIS; MALE; MIDDLE AGED; MOLECULAR SIZE; MOUSE; NONHUMAN; PROTEINACEOUS; SIZE EXCLUSION CHROMATOGRAPHY; STRUCTURE ANALYSIS; TISSUE DISTRIBUTION; TISSUE STRUCTURE; TRANSMISSION ELECTRON MICROSCOPY; ANIMAL; C57BL MOUSE; CHEMISTRY; PIG; SPECIES DIFFERENCE; ULTRASTRUCTURE;

AGED; ANIMALS; CHROMATOGRAPHY, GEL; FEMALE; HUMANS; HYDROLYSIS; LIVER GLYCOGEN; MALE; MICE; MICE, INBRED C57BL; MIDDLE AGED; MOLECULAR STRUCTURE; SPECIES SPECIFICITY; SWINE;

EID: 84961774444     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0150540     Document Type: Article

References (20)

1. Smythe C, Villar-Palasi C, Cohen P. Structural and functional studies on rabbit liver glycogenin. Eur J Biochem. 1989;183:205-9. doi: 10.1111/j.1432-1033.1989.tb14914.x PMID: 2526735
2. Meyer F, Heilmeyer L, Haschke RH, Fischer EH. Control of phosphorylase activity in a muscle glycogen particle. 1. Isolation and characterization of protein-glycogen complex. Journal of Biological Chemistry. 1970;245(24):6642-8. PMID: WOS:A1970I077500022.
3. Rybicka KK. Glycosomes-The organelles of glycogen metabolism. Tissue Cell. 1996;28(3):253-65. PMID: 8701432
4. Newsholme EA, Start C. Regulation of metabolism. New York: Wiley; 1974.
5. Drochmans P. Study under the electron microscope of negative colourings of particulate glycogen. J Ultrastructural Res. 1962;6:141-63.
6. Sullivan MA, Li J, Li C, Vilaplana F, Zheng L, Stapleton D, et al. Molecular structural differences between type-2-diabetic and healthy glycogen. Biomacromolecules. 2011;12(6):1983-6. doi: 10.1021/bm2006054 PMID: 21591708
7. Deng B, Sullivan MA, Li J, Tan X, Zhu C, Schulz BL, et al. Molecular structure of glycogen in diabetic liver. Glycoconjugate Journal. 2015;32(3-4):113-8. doi: 10.1007/s10719-015-9578-6 PMID: 25796617
8. Sullivan MA, Aroney STN, Li S, Warren FJ, Joo L, Mak KS, et al. Changes in glycogen structure over feeding cycle sheds new light on blood-glucose control. Biomacromolecules. 2014;15(2):660-5. doi: 10.1021/bm401714v PMID: 24372590
9. Orrell SA, Bueding E. A comparison of products obtained by various procedures used for the extraction of glycogen. J Biol Chem. 1964;239(12):4021-6.
10. Geddes R, Stratton GC. Molecular and metabolic heterogeneity of liver glycogen. Carbohydr Res. 1977;57:291-9. doi: 10.1016/s0008-6215 (00) 81938-2 PMID: 902278
11. Powell PO, Sullivan MA, Sheehy JJ, Schultz BL, Warren FJ, Gilbert RG. Acid hydrolysis and molecular density of phytoglycogen and liver glycogen helps with understanding the bonding in alpha (composite) glycogen molecules. PLoS One. 2015;10(3):e0121337. doi: 10.1371/journal.pone.0121337
12. Roehrig KL, Allred JB. Direct Enzymatic Procedure for the Determination of Liver Glycogen. Anal Biochem. 1974;58:414-21. PMID: 4827390
13. Sullivan MA, Powell PO, Witt T, Vilaplana F, Roura E, Gilbert RG. Improving size-exclusion chromatography for glycogen. J Chromatography A. 2014;1332(1):21-9. doi: 10.1016/j.chroma.2014.01.053
14. Sullivan MA, O'Connor MJ, Umana F, Roura E, Jack K, Stapleton DI, et al. Molecular Insights into Glycogen Alpha-Particle Formation. Biomacromolecules. 2012;13(11):3805-13. doi: 10.1021/bm3012727 PMID: 23004915
15. Sullivan MA, Li S, Aroney ST, Deng B, Li C, Roura E, et al. A rapid extraction method for glycogen from formalin-fixed liver. Carbohydrate Polymers. 2015;118(1):9-15. doi: 10.1016/j.carbpol.2014.11.005
16. Deng B, Sullivan MA, Wu AC, Li J, Chen C, Gilbert RG. The mechanism for stopping chain and totalmolecule growth in complex branched polymers, exemplified by glycogen. Biomacromolecules. 2015;16(6):1870-2. doi: 10.1021/acs.biomac.5b00459 PMID: 25933040
17. Melendez R, Melendez-Hevia E, Mas F, Mach J, Cascante M. Physical Constraints in the Synthesis of Glycogen That Influence Its Structural Homogeneity: A Two-Dimensional Approach. Biophys J. 1998;75(1):106-14. doi: 10.1016/S0006-3495 (98) 77498-3 PMID: 9649371
18. Besford QA, Zeng X-Y, Ye J-M, Gray-Weale A. Liver glycogen in type 2 diabetic mice is randomly branched as enlarged aggregates with blunted glucose release. Glycoconjugate Journal. 2015; in press: 1-11. doi: 10.1007/s10719-015-9631-5
19. Galinsky G, Burchard W. Starch fractions as examples for nonrandomly branched macromolecules. 3. Angular dependence in static light scattering. Macromolecules. 1997;30(15):4445-53. doi: 10.1021/ma961775o PMID: AN1997:429623.
20. Yang C, Meng B, Chen M, Liu X, Hua Y, Ni Z. Laser-light-scattering study of structure and dynamics of waxy com amylopectin in dilute aqueous solution. Carbohydrate Polymers. 2006;64(2):190-6. doi: 10. 1016/j.carbpol.2005.11.017