Contact: Janet Lathrop
University of Massachusetts at Amherst
Caption: Tew and colleagues have found a way not only to get inside na´ve T cells, but to deliver bio-active cargo such as proteins and synthetic molecules across that long-locked cell membrane, by using a new synthetic protein transduction domain that mimics natural ones.
Credit: UMass Amherst
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Related news release: UMass Amherst research scores advance in manipulating T-cells