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PMC:7795856 / 20693-22034 JSONTXT

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LitCovid-PubTator

Id Subject Object Predicate Lexical cue tao:has_database_id
359 389-404 Gene denotes thymosin beta 4 Gene:7114
360 418-444 Gene denotes C-type natriuretic peptide Gene:4880
361 446-449 Gene denotes CNP Gene:4880
362 463-482 Gene denotes parathyroid hormone Gene:5741
363 484-487 Gene denotes PTH Gene:5741
364 512-535 Gene denotes glucagon-like peptide-1 Gene:2641
365 537-542 Gene denotes GLP-1 Gene:2641
366 1020-1042 Gene denotes dipeptidyl peptidase-4 Gene:1803
367 1044-1050 Gene denotes DPP-IV Gene:1803
368 1090-1095 Gene denotes GLP-1 Gene:2641
369 457-462 Species denotes human Tax:9606

LitCovid-sentences

Id Subject Object Predicate Lexical cue
T117 0-119 Sentence denotes The beneficial application of the PASylation technology demonstrated in this work can be transferred to other peptides.
T118 120-335 Sentence denotes There are more than 7000 naturally occurring peptides covering a wide range of physiological functions [61], including many peptides with proven therapeutic potential, which could profit from the presented approach.
T119 336-565 Sentence denotes Examples are therapeutically active peptides such as thymosin beta 4 [62,63], the C-type natriuretic peptide (CNP) [64], human parathyroid hormone (PTH) [65], relaxin [66], or glucagon-like peptide-1 (GLP-1) and its analogs [67].
T120 566-793 Sentence denotes Today, it is generally recognized that intrinsic weaknesses of this drug class, such as poor stability and short circulating plasma half-life, need to be addressed in order to transform peptides into efficacious medicines [61].
T121 794-902 Sentence denotes The approach described here, N- or C-terminal PASylation, optionally combined with acetylation, solves both.
T122 903-1101 Sentence denotes On the one hand, N-terminal acetylation protects peptides from proteolytic degradation by exoproteases, for example, dipeptidyl peptidase-4 (DPP-IV), as shown for N-terminally acetylated GLP-1 [68].
T123 1102-1341 Sentence denotes On the other hand, PASylation increases the hydrodynamic volume of the peptide above the pore size of the glomerular basement membrane, hence retarding kidney filtration and prolonging the pharmacodynamic effect of its fusion partner [31].