نتایج جستجو برای: β peptide

تعداد نتایج: 328916  

Peptides are one of the best candidates for drug development due to their high specificity and low toxicity and porphyrins are significant macromolecules in biological systems with important roles. In this works ynthesis of dipeptide (histidine-β-alanine) was done by solid-phase peptide synthesis method (SPPS) and tetrakis(4-sulfonatophenyl)porphyrin (TPPS4) was synthesized by Adler method. The...

2013
Sara Garcia-Ratés Matthew Lewis Rosemary Worrall Susan Greenfield

BACKGROUND β-amyloid is regarded as a significant factor in Alzheimer's disease: but inefficient therapies based on this rationale suggests that additional signalling molecules or intermediary mechanisms must be involved in the actual initiation of the characteristic degeneration of neurons. One clue could be that acetylcholinesterase, also present in amyloid plaques, is aberrant in peripheral ...

Journal: :modares journal of medical sciences: pathobiology 2015
saeedeh ghiasvand fatemeh rahbarizadeh majid sadeghizadeh

background: prostate cancer after lung cancer is the second cause of cancer-associated death in men. in recent years, targeted therapy of cancer has attracted researchers attention. the targeted therapy lead to decrease in side effects of drugs. studies have indicated that targeting peptides for cancer cells represent valuable tools for diagnostic and therapeutic. recently, phage display peptid...

2014
Ji Eun Lee Ji Woo Lee Tatsuyoshi Fujii Noriyoshi Fujii Jong Weon Choi

OBJECTIVE This study investigated the use of the estimated average glucose to fasting plasma glucose ratio (eAG/fPG ratio) to screen for β-cell function in pediatric diabetes. METHODS Glycated hemoglobin (HbA1c), glycated albumin (GA), fructosamine, insulin, and C-peptide levels were measured. The ratio of GA to HbA1c (GA/A1c ratio) was calculated, and the homeostasis model assessment of β-ce...

2015
Zichen Luo Jie Bao

Background: Zymomonas mobilis is an efficient ethanol fermentation strain, but its narrow substrate range limits its fermentation in lignocellulose hydrolysate. As a potential consolidated bioprocessing (CBP) stain for bioethanol production, the ability of cellulose utilization was necessary. In this study, extracellular expression of β-glucosidase on Z. mobilis was studied as the first step fo...

2014
Birgit Eisenhaber Stephan Eisenhaber Toh Yew Kwang Gerhard Grüber Frank Eisenhaber

The transamidase subunit GAA1/GPAA1 is predicted to be the enzyme that catalyzes the attachment of the glycosylphosphatidyl (GPI) lipid anchor to the carbonyl intermediate of the substrate protein at the ω-site. Its ~300-amino acid residue lumenal domain is a M28 family metallo-peptide-synthetase with an α/β hydrolase fold, including a central 8-strand β-sheet and a single metal (most likely zi...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه علامه طباطبایی 1388

عاملهای شناختی، شخصیتی و موقعیتی متعددی یافت شده است که می توانند با پرخاشگری ارتباط داشته باشند. فهم چگونگی ارتباط درونی این عاملها برای پیش بینی، سنجش، و درمان پرخاشگری زندانیانی که سابقه رفتارهای پرخاشگرانه را دارند، بسیار اساسی است. پژوهشهای قبلی نقش بالقوه ای را برای توانایی حل مساله اجتماعی بعنوان یک میانجیگر بین تکانشگری و پرخاشگری پیشنهاد کرده اند. ( موران و همکاران، 2002). علاوه بر این...

Journal: :Food production, processing and nutrition 2021

Abstract Food components possessing zinc ligands can be used to inhibit zinc-dependent enzymes. In this study, zinc-binding peptides were derived from whey protein hydrolysates, and their ultrafiltration (> 1 < kDa) fractions, produced with Esperase (WPH-Esp), Everlase Savinase. Immobilized metal affinity chromatography (IMAC-Zn 2+ ) increased the capacity of peptide fraction (83%) when c...

Journal: :Organic & biomolecular chemistry 2011
Sylvain Aubry Kaname Sasaki Laure Eloy Geneviève Aubert Pascal Retailleau Thierry Cresteil David Crich

A series of novel peptide-based β-thiolactones were synthesized and assayed for cytotoxicity against several human cancer cell lines, where they showed greater activity than the corresponding β-lactones and β-lactams. Several of the β-thiolactones prepared showed strong inhibitory activity in vitro against human cathepsins B and L.

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