Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành hóa học dành cho các bạn yêu hóa học tham khảo đề tài: Inhibition of Henipavirus fusion and infection by heptad-derived peptides of the Nipah virus fusion glycoprotein
"Bioactive Food Peptides in Health and Disease" highlights recent developments on bioactive food peptides for the promotion of human health and the prevention/management of chronic diseases. The book provides a comprehensive revision of bioactive peptides obtained from both animal and plant food sources. Aspects related to their bioactivity, mechanism of action, and bioavailability are extensively described along the different chapters.
Tuyển tập các báo cáo nghiên cứu về y học được đăng trên tạp chí y học General Psychiatry cung cấp cho các bạn kiến thức về ngành y đề tài: Effect of dsDNA binding to SmD-derived peptides on clinical accuracy in the diagnosis of systemic lupus erythematosus...
Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành y học dành cho các bạn tham khảo đề tài: Salivary gland derived peptides as a new class of anti-inflammatory agents: review of preclinical pharmacology of C-terminal peptides of SMR1 protein...
Research on cell-penetrating peptides for the intracellular delivery of por-phyrin compounds has mainly focused on the use of trans-activator of
transcription (TAT)-derived peptides and, to a lesser extent, on proline-rich
peptides and phosphorescent metalloporphyrins. In this article, we describe
a novel phosphorescent oxygen-sensitive probe for intracellular use which
comprises a bactenecin 7 peptide fragment (15–24) conjugated with the
uncharged monofunctional derivative of Pt(II) coproporphyrin I (PEPP0)....
Macrophages at an inflammatory site release massive
amounts of proteolytic enzymes, including lysosomal cys-teine proteases, which colocalizewith their circulating, tight-binding inhibitors (cystatins, kininogens), so modifying the
protease/antiprotease equilibrium in favor of enhanced
proteolysis. We have explored the ability of human cath-epsins B, KandL to participate in the production of kinins,
using kininogens and synthetic peptides that mimic the
insertion sites of bradykinin on human kininogens....
A small amino acid sequence (LWYIK) inside the HIV-1 gp41 ectodomain
membrane proximal region (MPR) is commonly referred to as a choles-terol-binding domain. To further study this unique and peculiar property
we have used fluorescence spectroscopy techniques to unravel the mem-brane interaction properties of three MPR-derived synthetic peptides: the
membrane proximal region peptide-complete (MPRP-C) which corresponds
to the complete MPR;
Several hematopoietic growth factors (HGFs) have achieved widespread clinical
application. In the United States alone, more than US $5 billion per year of the health care
budget is spent on these factors. The first patients were treated with recombinant human
erythropoietin (rHuEPO, epoetin alfa, Epogen®) in 1985 and the first patients received
recombinant methionyl human granulocyte colony-stimulating factor (r-metHuG-CSF,
filgrastim, Neupogen®) or recombinant human granulocyte-macrophage colonystimulating
factor (rHuGM-CSF, sargramostim, Leukine® or Prokine®) in 1986.
Tuyển tập các báo cáo nghiên cứu về y học được đăng trên tạp chí y học General Psychiatry cung cấp cho các bạn kiến thức về ngành y đề tài: Immunization with an immunodominant self-peptide derived from glucose-6-phosphate isomerase induces arthritis in DBA/1 mice...
Numerous proteins cannot be sufficiently prepared by ordinary recombi-nant DNA techniques because they are unstable or have deleterious effects
on the host cell. One idea to prepare such proteins is to produce them as
protein inclusions. Here we developed a novel system to effectively prepare
proteins by using peptide tags derived from the insecticidal Cry toxin of a
soil bacterium, Bacillus thuringiensis.
a-Conotoxins are small peptides from cone snail venoms that function as
nicotinic acetylcholine receptor (nAChR)-competitive antagonists differenti-ating between nAChR subtypes. Current understanding about the mechan-ism of these selective interactions is based largely on mutational analyses,
which identify amino acids in the toxin and nAChR that determine the
energetics of ligand binding.
(BQ) Part 2 book "Organic chemistry" has contents: Reactions of carboxylic acids and carboxylic derivatives, reactions of benzene and substituted benzenes, reactions of heterocyclic compounds, the organic chemistry of carbohydrates, the organic chemistry of amino acids, peptides, and proteins,... and other contents.
Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành hóa học dành cho các bạn yêu hóa học tham khảo đề tài: Fibrillar beta-amyloid peptide Aβ1–40 activates microglial proliferation via stimulating TNF-α release and H2O2 derived from NADPH oxidase: a cell culture study
Phage display technology is a powerful selection approach to identify
strong and specific binders to a large variety of targets. In this study, we
compared the efficacy of a phage library displaying human heavy chain
complementarity determining region 3 (HCDR3) repertoires with a set of
conventional random peptide libraries for the identification of CXCR4
The bioactive dipeptide derivative anserine (b-alanyl-1-N-methyl-l-histidine)
is absorbed from the human diet in intact form at the intestinal epithelium.
The purpose of this study was to investigate whether anserine is a substrate
of the H
⁄peptide cotransporters 1 and 2 (PEPT1 and PEPT2).
In the present study, EA-CATH1 and EA-CATH2 were identified from
a constructed lung cDNA library of donkey (Equus asinus) as members
of cathelicidin-derived antimicrobial peptides, using a nested PCR-based
cloning strategy. Composed of 25 and 26 residues, respectively,
EA-CATH1 and EA-CATH2 are smaller than most other cathelicidins
and have no sequence homology to other cathelicidins identified to date.
The cathelicidin antimicrobial peptide bactenecin is ab-hairpin molecule
with a single disulfide bond and broad antimicrobial activity. The proform
of bactenecin exists as a dimer, however, and it has been proposed that
bactenecin is released as a dimer in vivo, although there has been little
study of the dimeric form of bactenecin.