Sentence examples for molecules for recognition from inspiring English sources

The interlayer space of dysprosium containing LDH was successfully intercalated with folate, ibuprofen and gallate ions, which are key molecules for recognition of some cancer cells and treatment of diseases.

In this work, a series of bipyridine core D(A′ -π-A-π-D(A′ -π-A-π-Do–photon A′ -π-A-π-D(TPA′ -π-A-π-Dence probe molecules for recognition of Zn2+ hA′ -π-A-π-Dudied by the density functionA′ typery (DFtwo photone dependent-DFT (TD-DFT).

However, it has to be further clarified whether the antigen processing machinery of pluripotent stem cells is capable of generating peptide loaded MHC class I molecules for recognition by activated CTLs.

Taken together, these observations suggest that the VR2 region contains common binding determinants utilized in both SIVmnd-2 and SIVsmm type Vpx molecules for recognition of SAMHD1-NtD and SAMHD1-CtD degrons.

In the case of cancer vaccines, the antigens typically are not foreign, but overexpressed self-antigens on the surface or inside the tumor cell, some of which are then presented on the cell surface in the context of HLA molecules for recognition by T-cells.

Similarly, although the introduction of nucleotide insertions and/or deletions is inherent to the CRISPR engineering process, it is extremely improbable that they would in all cases inadvertently lead to the generation of neo-self determinants that can be efficiently processed and presented on H-2 MHC class I molecules for recognition by CD8+ T cells.

The APC processes the antigens, and the immunogenic peptide is then presented at the cell surface along with the MHC molecule for recognition by the TCR.

All identified epitope variants were synthesized as peptides and tested for binding to the disease-associated HLA-DQ2 and HLA-DQ8 molecules and for recognition by patient-derived α-gliadin specific T cell clones.

Indeed, mice with deficiencies in molecules critical for recognition, internalization, or lysosomal DNA degradation of apoptotic cells, including C1q, C4, IgM, the pentraxin Serum Amyloid P, MerTK, milk fat globule protein-E8, clAscavengerengereceptorsrs, or lysosomal DNase II develop systemic autoimmune disorders [ 60– 60].

These binding properties render lipocalins suitable candidate molecules for kin recognition.

The major histocompatibility complexes (MHCs) are often considered to be the main functioning molecules for immune recognition.