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Cell penetrating peptides (CPPs) are able to route across cells' membrane various types of cargo, including drugs and nanoparticles.
KIFs can transport various types of cargo, including organelles, synaptic vesicle precursors, neurotransmitter receptors, cell signaling molecules, cell adhesion molecules, and mRNAs in neurons of mammalian nervous system [ 24, 25].
Gold nanoparticles such as NG and CG have been shown to improve biocompatibility and enhance cellular uptake of various types of cargo in drug delivery applications [ 44, 45, 53, 54].
Arginine-rich peptides have been extensively used to enhance cellular uptake of various types of cargo, and there is a reasonable presumption that they can deliver cargo out of subcellular compartments as well although there is little information on this point.
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We first describe the nature of versatile CPPs and their interactions with various types of cargoes.
These peptides have been used to deliver various types of cargoes such as proteins, peptide, siRNA, liposomes, nanoparticles and drugs (11).
The large elastic deformability of graphene and the van Der Waals nature of the transport force allow for programmable directional transport of various types of molecular cargo (e.g., graphene flake, carbon nanotube, fullerene, and gold nanoparticle) under the same mechanism.
It seems, therefore, that Ubp2 has a role in modulating Rsp5-mediated trafficking of various types of membrane associated cargo.
EVs are involved in NAFLD pathology because they regulate cell-cell communication and a number of pathophysiological events in various types of cells via horizontal transfer of their cargo including proteins (membrane, cytosolic, and nuclear), RNAs (including mRNAs and microRNAs), and lipids (Yuan et al., 2009, Diehl et al., 2012, Raposo and Stoorvogel, 2013).
It is well known that distinct type of cells can express almost all the importins (highly conserved among various types of cells) that involved in the transport of cargos [ 47, 48].
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