Study on Saccharide-Glucose Receptor Interactions with the Use of Surface Plasmon Resonance.
angiostatics
biosensors
nanoparticles
saccharides
surface plasmon resonance
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
08 Nov 2023
08 Nov 2023
Historique:
received:
11
09
2023
revised:
19
10
2023
accepted:
06
11
2023
medline:
27
11
2023
pubmed:
25
11
2023
entrez:
25
11
2023
Statut:
epublish
Résumé
The aim of this study was to investigate the process of attachment of saccharide particles differing in degree of complexity to cell receptors responsible for transport of glucose across the cell membrane (GLUT proteins). This phenomenon is currently considered when designing modern medicines, e.g., peptide drugs to which glucose residues are attached, enabling drugs to cross the barrier of cell membranes and act inside cells. This study aims to help us understand the process of assimilation of polysaccharide nanoparticles by tumour cells. In this study, the interactions between simple saccharides (glucose and sucrose) and dextran nanoparticles with two species of GLUT proteins (GLUT1 and GLUT4) were measured using the surface plasmon resonance technique. We managed to observe the interactions of glucose and sucrose with both applied proteins. The lowest concentration that resulted in the detection of interaction was 4 mM of glucose on GLUT1. Nanoparticles were measured using the same proteins with a detection limit of 40 mM. These results indicate that polysaccharide nanoparticles interact with GLUT proteins. The measured strengths of interactions differ between proteins; thus, this study can suggest which protein is preferable when considering it as a mean of nanoparticle carrier transport.
Identifiants
pubmed: 38003267
pii: ijms242216079
doi: 10.3390/ijms242216079
pmc: PMC10671554
pii:
doi:
Substances chimiques
Glucose
IY9XDZ35W2
glucose receptor
0
Glucose Transporter Type 1
0
Carbohydrates
0
Glucose Transport Proteins, Facilitative
0
Sucrose
57-50-1
Glucose Transporter Type 4
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : National Science Centre, Poland
ID : 2017/25/N/ST8/01027
Références
J Mater Chem B. 2023 May 24;11(20):4428-4444
pubmed: 37067506
Int J Pharm. 2023 Apr 25;637:122894
pubmed: 36990168
J Pharm Anal. 2018 Jun;8(3):147-152
pubmed: 29922482
J Cell Biochem. 2010 Dec 1;111(5):1252-9
pubmed: 20803547
J Chromatogr A. 1997 Jul 25;776(1):87-91
pubmed: 9286081
PLoS One. 2011;6(9):e25237
pubmed: 21966466
Biochem Genet. 2005 Apr;43(3-4):175-87
pubmed: 15932065
Drug Discov Today. 2010 Oct;15(19-20):842-50
pubmed: 20727417
Int J Endocrinol. 2010;2010:
pubmed: 20706540
Int J Biol Macromol. 2019 Sep 1;136:266-274
pubmed: 31201909
Anal Chim Acta. 2012 Jan 27;712:9-29
pubmed: 22177061
Science. 2009 May 22;324(5930):1029-33
pubmed: 19460998
Int J Mol Sci. 2021 Jun 21;22(12):
pubmed: 34205578
J Exp Med. 2012 Feb 13;209(2):211-5
pubmed: 22330683
Carbohydr Polym. 2019 Oct 1;221:94-112
pubmed: 31227171
PLoS One. 2016 Jan 11;11(1):e0146237
pubmed: 26752182
Cell Death Dis. 2013 Mar 07;4:e532
pubmed: 23470539
J Am Chem Soc. 2012 Feb 8;134(5):2681-90
pubmed: 22229911
Curr Genomics. 2007 Apr;8(2):113-28
pubmed: 18660845
J Mater Chem B. 2021 Sep 15;9(35):7030-7062
pubmed: 33928990
Adv Drug Deliv Rev. 2005 Feb 28;57(4):609-36
pubmed: 15722167
Methods Mol Biol. 2016;1406:289-302
pubmed: 26820964