NTA-Co3+-His6 versus NTA-Ni2+-His6 mediated E-Cadherin surface immobilization enhances cellular traction. (February 2019)
- Record Type:
- Journal Article
- Title:
- NTA-Co3+-His6 versus NTA-Ni2+-His6 mediated E-Cadherin surface immobilization enhances cellular traction. (February 2019)
- Main Title:
- NTA-Co3+-His6 versus NTA-Ni2+-His6 mediated E-Cadherin surface immobilization enhances cellular traction
- Authors:
- Di Russo, Jacopo
Young, Jennifer L.
Balakrishnan, Adithya
Benk, Amelie S.
Spatz, Joachim P. - Abstract:
- Abstract: Understanding the biological impact of strategies for protein immobilization onto bioactive surfaces is crucial for the design of biomimetic materials. A common strategy used to immobilize or label recombinant proteins is to exploit the Ni 2+ -mediated interaction of nitrilotriacetic acid (NTA) with the hexahistidine tag (His6 -tag) present on recombinant proteins. While this method ensures a controlled orientation and functionality of the protein, the kinetically labile nature of the bond ensures only its weak immobilization onto the surface. Recently, it has been shown that the oxidation of Co 2+ to Co 3+ greatly stabilizes the bond between NTA and the His6 -tagged proteins, making it inert to ligand exchange and resistant to chelators. This approach not only has the potential to improve the quality of biomimetic material functionalization and molecule labeling but could also affect cellular mechanical responses for which the mechanical strength of the protein-surface bond is crucial. Here, we compared gold (Au) nanopatterned polyacrylamide (PAA) hydrogels functionalized with E-cadherin via Co 3+ with those functionalized via Ni 2+ for studying adhesion-mediated responses in keratinocytes. We show that keratinocytes develop higher and a broader range of adhesion forces, leading to extended cell spreading and colony organization on Co 3+ vs. Ni 2+ . This work uniquely shows that stabilizing the NTA/His6 -tag bond via Co 3+ for protein immobilization significantlyAbstract: Understanding the biological impact of strategies for protein immobilization onto bioactive surfaces is crucial for the design of biomimetic materials. A common strategy used to immobilize or label recombinant proteins is to exploit the Ni 2+ -mediated interaction of nitrilotriacetic acid (NTA) with the hexahistidine tag (His6 -tag) present on recombinant proteins. While this method ensures a controlled orientation and functionality of the protein, the kinetically labile nature of the bond ensures only its weak immobilization onto the surface. Recently, it has been shown that the oxidation of Co 2+ to Co 3+ greatly stabilizes the bond between NTA and the His6 -tagged proteins, making it inert to ligand exchange and resistant to chelators. This approach not only has the potential to improve the quality of biomimetic material functionalization and molecule labeling but could also affect cellular mechanical responses for which the mechanical strength of the protein-surface bond is crucial. Here, we compared gold (Au) nanopatterned polyacrylamide (PAA) hydrogels functionalized with E-cadherin via Co 3+ with those functionalized via Ni 2+ for studying adhesion-mediated responses in keratinocytes. We show that keratinocytes develop higher and a broader range of adhesion forces, leading to extended cell spreading and colony organization on Co 3+ vs. Ni 2+ . This work uniquely shows that stabilizing the NTA/His6 -tag bond via Co 3+ for protein immobilization significantly impacts cellular phenotype on biomimetic materials by impacting cell signaling. … (more)
- Is Part Of:
- Biomaterials. Volume 192(2019)
- Journal:
- Biomaterials
- Issue:
- Volume 192(2019)
- Issue Display:
- Volume 192, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 192
- Issue:
- 2019
- Issue Sort Value:
- 2019-0192-2019-0000
- Page Start:
- 171
- Page End:
- 178
- Publication Date:
- 2019-02
- Subjects:
- Cobalt -- Nitrilotriacetic acid -- E-Cadherin -- Traction-force -- Cell adhesion -- Surface functionalization
Biomedical materials -- Periodicals
Biocompatible Materials -- Periodicals
Biomatériaux -- Périodiques
610.28 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01429612 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/01429612 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/01429612 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.biomaterials.2018.10.042 ↗
- Languages:
- English
- ISSNs:
- 0142-9612
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2087.715000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21517.xml