Biotin-Avidin-Mediated Capture of Microspheres on Polymer Fibers.
avidin
bioreactor
biorthogonal
biotin
particle capture
polymer mesh
Journal
Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009
Informations de publication
Date de publication:
28 May 2019
28 May 2019
Historique:
received:
16
04
2019
revised:
09
05
2019
accepted:
23
05
2019
entrez:
31
5
2019
pubmed:
31
5
2019
medline:
21
11
2019
Statut:
epublish
Résumé
Systems for efficient and selective capture of micro-scale objects and structures have application in many areas and are of particular relevance for selective isolation of mammalian cells. Systems for the latter should also not interfere with the biology of the cells. This study demonstrates the capture of microspheres through orthogonal coupling using biotin (ligand) and (strept)avidin (receptor). Fibrous poly(ethylene terephthalate) (PET) meshes were hydrolyzed under controlled alkaline conditions to obtain activated surfaces with COOH groups allowing for the functionalization of the PET with biotin of various spacer length. The system capture efficiency was optimized by varying the length of spacer presenting the biotin against streptavidin. In a proof of concept experiment, avidin-functionalized microspheres were used as surrogates for cells, and their capture under dynamic conditions including virous mixing and high-flow rate perfusion is demonstrated. Functionalization of PET meshes with biotin conjugated to longest spacer yielded the most efficient capture of microspheres. These preliminary results lay the foundation for the development of biosystems for capture of specific cells under physiologically relevant conditions, using biorthogonal avidin-biotin interactions.
Identifiants
pubmed: 31141958
pii: molecules24112036
doi: 10.3390/molecules24112036
pmc: PMC6600533
pii:
doi:
Substances chimiques
Alkalies
0
Polyethylene Terephthalates
0
Polymers
0
Avidin
1405-69-2
Biotin
6SO6U10H04
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Deutsche Forschungsgemeinschaft
ID : EXC 294
Références
Ann Biomed Eng. 2008 Apr;36(4):604-21
pubmed: 18299992
J Chromatogr A. 2007 Aug 31;1162(2):154-61
pubmed: 17561026
Annu Rev Anal Chem (Palo Alto Calif). 2010;3:409-31
pubmed: 20636049
Proc Natl Acad Sci U S A. 2008 Nov 25;105(47):18165-70
pubmed: 19015523
Gene Ther. 2003 Dec;10(25):2090-7
pubmed: 14595382
J Nanobiotechnology. 2015 May 16;13:37
pubmed: 25980573
Biophys J. 2002 Jun;82(6):3214-23
pubmed: 12023246
Lab Chip. 2017 May 16;17(10):1769-1777
pubmed: 28394386
Biomed Mater. 2010 Oct;5(5):054112
pubmed: 20876956
Biophys J. 1997 Apr;72(4):1568-81
pubmed: 9083662
J Mater Chem B. 2017 Jun 28;5(24):4745-4753
pubmed: 32264317
Cancer J. 2018 Mar/Apr;24(2):70-77
pubmed: 29601333
Biomaterials. 2007 Dec;28(36):5471-6
pubmed: 17869335
Langmuir. 2010 Jan 19;26(2):809-14
pubmed: 19725548
Proc Natl Acad Sci U S A. 1989 Apr;86(7):2190-4
pubmed: 2928324
J Biomed Mater Res. 2001 Nov;57(2):183-9
pubmed: 11484180
Semin Immunopathol. 2011 May;33(3):235-43
pubmed: 21225262
Biotechnol Bioeng. 2003 Oct 20;84(2):205-14
pubmed: 12966577
Clin Chem. 1991 May;37(5):625-36
pubmed: 2032315
Biomaterials. 1997 Nov;18(21):1417-24
pubmed: 9375843
PLoS One. 2014 Nov 10;9(11):e112292
pubmed: 25383949
Biotechnol Prog. 1999 Mar-Apr;15(2):238-44
pubmed: 10194399
Eur Surg Res. 2003 May-Jun;35(3):161-6
pubmed: 12740536
Langmuir. 2004 Jun 22;20(13):5493-500
pubmed: 15986691
Biophys J. 1996 Mar;70(3):1391-401
pubmed: 8785294
Anal Biochem. 1994 Apr;218(1):87-91
pubmed: 8053572
Anal Biochem. 1986 Jul;156(1):220-2
pubmed: 3740412
Biomaterials. 2001 Jan;22(2):151-63
pubmed: 11101159
Science. 1942 Sep 11;96(2489):257
pubmed: 17770530
Anal Biochem. 1989 Aug 1;180(2):253-8
pubmed: 2817353
Comput Methods Programs Biomed. 2008 Oct;92(1):135-43
pubmed: 18653259