Peptide Scanning for Studying Structure-Activity Relationships in Drug Discovery

被引:75
作者
Jamieson, Andrew G. [2 ]
Boutard, Nicolas [3 ]
Sabatino, David [4 ]
Lubell, William D. [1 ]
机构
[1] Univ Montreal, Dept Chem, Montreal, PQ H3C 3J7, Canada
[2] Univ Leicester, Dept Chem, Leicester LE1 7RH, Leics, England
[3] Italian Inst Technol, Drug Discovery & Dev Dept, I-16163 Genoa, Italy
[4] Seton Hall Univ, Dept Chem & Biochem, S Orange, NJ 07079 USA
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
aza-amino acid; conformational constraint; Freidinger lactam; peptidomimetic; scan; stapled peptide; SOLID-PHASE SYNTHESIS; PROTEIN-PROTEIN INTERACTIONS; AZAAMINO ACID RESIDUE; HUMAN GROWTH-HORMONE; D-AMINO-ACID; SECONDARY STRUCTURE; N-METHYLATION; BINDING-SITE; AZA-PEPTIDES; LACTAM PEPTIDOMIMETICS;
D O I
10.1111/cbdd.12042
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Peptide-based therapeutics have grown in importance over the last few decades. Furthermore, peptides have been extensively used as lead compounds in the drug discovery process to investigate the nature of chemical space required for molecular recognition and activity at a variety of targets. This critical commentary reviews scanning techniques, which employ natural and non-proteinogenic amino acids to facilitate understanding of structural requirements for peptide biological activity. The value of sequence analysis by such methods is highlighted by examples, in which the elements for peptide affinity and activity have been elucidated and employed to prepare peptidomimetic leads for drug development.
引用
收藏
页码:148 / 165
页数:18
相关论文
共 107 条
  • [11] Aza-scanning of the potent melanocortin receptor agonist Ac-His-D-Phe-Arg-Trp-NH2
    Boeglin, D
    Xiang, Z
    Sorenson, NB
    Wood, MS
    Haskell-Luevano, C
    Lubell, WD
    [J]. CHEMICAL BIOLOGY & DRUG DESIGN, 2006, 67 (04) : 275 - 283
  • [12] Aza-amino acid scanning of secondary structure suited for solid-phase peptide synthesis with Fmoc chemistry and aza-amino acids with heteroatomic side chains
    Boeglin, D
    Lubell, WD
    [J]. JOURNAL OF COMBINATORIAL CHEMISTRY, 2005, 7 (06): : 864 - 878
  • [13] Calcitonin gene-related peptide analogues with aza and indolizidinone amino acid residues reveal conformational requirements for antagonist activity at the human calcitonin gene-related peptide 1 receptor
    Boeglin, Damien
    Hamdan, Fadi F.
    Melendez, Rosa E.
    Cluzeau, Jerome
    Laperriere, Andre
    Heroux, Madeleine
    Bouvier, Michel
    Lubell, William D.
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2007, 50 (06) : 1401 - 1408
  • [14] Targeting the Prostaglandin F2α Receptor for Preventing Preterm Labor with Azapeptide Tocolytics
    Bourguet, Carine B.
    Goupil, Eugenie
    Tassy, Danae
    Hou, Xin
    Thouin, Eryk
    Polyak, Felix
    Hebert, Terence E.
    Claing, Audrey
    Laporte, Stephane A.
    Chemtob, Sylvain
    Lubell, William D.
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2011, 54 (17) : 6085 - 6097
  • [15] Boutard N., 2009, BREAK AW P 21 AM PEP, P78
  • [16] Examination of the active secondary structure of the peptide 101.10, an allosteric modulator of the interleukin-1 receptor, by positional scanning using β-amino γ-lactams
    Boutard, Nicolas
    Turcotte, Stephane
    Beauregard, Kim
    Quiniou, Christiane
    Chemtob, Sylvain
    Lubell, William D.
    [J]. JOURNAL OF PEPTIDE SCIENCE, 2011, 17 (04) : 288 - 296
  • [17] Structure-Activity Analysis of the Growth Hormone Secretagogue GHRP-6 by α- and β-Amino γ-Lactam Positional Scanning
    Boutard, Nicolas
    Jamieson, Andrew G.
    Ong, Huy
    Lubell, William D.
    [J]. CHEMICAL BIOLOGY & DRUG DESIGN, 2010, 75 (01) : 40 - 50
  • [18] ON THE ACTIONS OF THE GROWTH HORMONE-RELEASING HEXAPEPTIDE, GHRP
    BOWERS, CY
    SARTOR, AO
    REYNOLDS, GA
    BADGER, TM
    [J]. ENDOCRINOLOGY, 1991, 128 (04) : 2027 - 2035
  • [19] N-Methylation of Peptides: A New Perspective in Medicinal Chemistry
    Chatterjee, Jayanta
    Gilon, Chaim
    Hoffman, Amnon
    Kessler, Horst
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 2008, 41 (10) : 1331 - 1342
  • [20] Conformationally constrained dipeptide surrogates with aromatic side-chains:: Synthesis of 4-aryl indolizidin-9-one amino acids by conjugate addition to a common α,ω-diaminoazelate enone intermediate
    Cluzeau, J
    Lubell, WD
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2004, 69 (05) : 1504 - 1512