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Problem of Diminished cRGD Surface Activity and What Can Be Done about It. | LitMetric

Problem of Diminished cRGD Surface Activity and What Can Be Done about It.

ACS Appl Mater Interfaces

Naval Research Laboratory, 4555 Overlook Ave SW, Washington, DC 20375-5320, United States.

Published: April 2020

AI Article Synopsis

Article Abstract

RGD peptides play a pivotal role in growing and diverse areas of biological research, ranging from experiments probing fundamental molecular mechanisms of cell adhesion to more applied strategies in medical imaging and cancer therapeutics. To better understand the outcomes of RGD-based approaches, we quantified the degree to which cyclic RGD (cRGD) activity is blocked by nonspecific binding of commonly used medium constituents. First, we show that recombinant αβ integrins can be used as a highly sensitive cell-free sensor to quantitatively and reliably characterize the activity of cRGD-functionalized surfaces surface plasmon resonance (SPR). Next, SPR experiments were utilized to measure the extent of blocking of cRGD-functionalized surfaces by the commonly used agents BSA, PLL--PEG, and fetal calf serum (FCS)-supplemented media, using recombinant αβ integrin as a probe for cRGD binding activity in the presence of blocking agents. All three additives were highly efficient blockers of cRGD activity, as exemplified by cell culture media containing 1% FCS which reduced the cRGD activity by 33-fold. We then developed a strategy to combat these deleterious effects by employing the recombinant integrins as a protective cap. We show that the unblocked cRGD activity can be preserved in the presence of PLL--PEG by employing the αβ integrin as a removable protective cap, both in cell-free and experiments. studies with MDA-MB-231 cells cultured atop cRGD-functionalized surfaces found that cell adhesion and migration prevented by PLL--PEG were restored when this protective cap approach was used.

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Source
http://dx.doi.org/10.1021/acsami.0c04340DOI Listing

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