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L1FLCD (1173 - 1185)

编号:434448

CAS号:

单字母:H2N-FGEYRSLESDNEE-OH

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  • 编号:434448
    中文名称:L1FLCD (1173 - 1185)
    英文名:L1FLCD (1173 - 1185)
    单字母:H2N-FGEYRSLESDNEE-OH
    三字母:H2N

    N端氨基

    -Phe

    苯丙氨酸

    -Gly

    甘氨酸

    -Glu

    谷氨酸

    -Tyr

    酪氨酸

    -Arg

    精氨酸

    -Ser

    丝氨酸

    -Leu

    亮氨酸

    -Glu

    谷氨酸

    -Ser

    丝氨酸

    -Asp

    天冬氨酸

    -Asn

    天冬酰胺

    -Glu

    谷氨酸

    -Glu

    谷氨酸

    -OH

    C端羧基

    氨基酸个数:13
    分子式:C66H95N17O28
    平均分子量:1574.56
    精确分子量:1573.65
    等电点(PI):4.24
    pH=7.0时的净电荷数:-2.02
    平均亲水性:0.925
    疏水性值:-1.68
    消光系数:1490
    标签:细胞粘附肽(Cell Adhesion Peptides)   

  • Discovery

    Synthetic cell adhesion peptides were first derived from laminin. The peptide PA22-2 (CSRARKQAASIKVAVSADR-NH2) derived from laminin was found to function as a cell adhesion molecule which was tested with mouse mast cells1.

    Classification

    Cell adhesion peptides for the most part are extracellular matrix proteins1.

    Structural Characteristics

    Numerous cell adhesion peptides have been synthesized to date.  Some examples include: RU-1 (LNIVSVNGRHX), RX-1 (DNRIRLQAKXX), GD-1 (KATPMLKMRTSFHGCIK), GD-2 (KEGYKVRLDLNITLEFRTTSK), GD-3 (KNLEISRSTFDLLRNSYGVRK), GD-6 (KQNCLSSRASFRGCVRNLRLSR), HGD-6 (KQKCLRSQTSFRGCLRKLALIK), SGD-6 (CRNRGRCNSSLFQVRSRKLLSA), HSGD-6 (KQCLKSQRSFTRGLCRLKAKIL), AG-1 (KLLISRARKQÁASIK), F17 (LERKYENDQKYLEDKA) and KRGD (VEKRGDREEA).  Peptides that are linear and cyclic in nature have been synthesized2.

    Mode of action

    Cell adhesion peptides can bind to the cell membrane and trigger adhesion of cells3.

    Functions

    Cell adhesion peptides have known to increase signaling via receptors3.  They have been shown to decrease tumor metastasis and growth in experimental animals3.  These peptides also induce Ca2+ signaling and modulate platelet activity3.

    References

    1.     Thompson HL, Burbelo PD,Yamada Y,Kleinman HK and Metcalfe DD (1991). Identification of an amino acid sequence in the laminin A chain mediating mast cell attachment and spreading, Immunology, 72, 144-149.

    2.     Gehlsen KR, Sriramarao P, Furcht LT and Skubitzt APN (1992).  A Synthetic Peptide Derived from the Carboxy Terminus of the Laminin A Chain Represents a Binding Site for the a3ß1 Integrin, J Cell Biology,117 (2), 449-459.

    3.     Book: Proteins analysis and design, Angeletti RH, 222-226.

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