专肽生物_定制多肽合成服务_多肽合成定制服务_多肽合成厂家_多肽合成公司

人肾上腺髓质素前体（153-185）包含引导正确折叠和转化为成熟肽形式的基序。侧链聚类支持分类、加工和分泌贩运的研究。构象映射揭示了前体组装的中间阶段。

Prepro-adrenomedullin (153-185), human, encompasses motifs guiding proper folding and conversion to mature peptide forms. Side-chain clustering supports studies on sorting, processing, and secretory trafficking. Conformational mapping reveals intermediate stages of precursor assembly. 

人前肾上腺髓质素原（153‑185）包含指导正确折叠并转化为成熟多肽的结构基序。侧链聚集特性可用于分选、加工与分泌转运研究；构象图谱可揭示前体组装的中间阶段。研究者将其用于生物合成、代谢建模与多肽设计。

Prepro-adrenomedullin (153-185), human, encompasses motifs guiding proper folding and conversion to mature peptide forms. Side-chain clustering supports studies on sorting, processing, and secretory trafficking. Conformational mapping reveals intermediate stages of precursor assembly. Researchers utilize this fragment in biosynthesis, metabolic modeling, and peptide design work.

Definition
Adrenomedullin (AM) is a pluripotent peptide and a hypotensive substance extracted from human adrenal tumour. Due to its origin of discovery, i.e. the medulla of the adrenal gland, the peptide is named adrenomedullin.
Discovery
AM was initially isolated from phaechromcytoma cells in 1993 by Kitmura K and his associates1.

Classification
AM is a member of the calcitonin family of peptides. In teleost fish, AM forms an independent subfamily consisting of five members viz. (AM1–AM5). This teleost AM family comprises three groups, AM1/AM4, AM2/AM3, and AM5 2,3.

Structural Characteristics
The peptide consists of 52 amino acids with a 6-member ring structure linked by a disulfide bond between amino acid 16 and 21 and amidated-COOH terminal4. It has 27 % homology with the calcitonin gene-related peptide (CGRP).

Mechanism of action
AM peptides act through specific receptors in the plasma membrane to activate adenylate cyclase activity and modulate Ca2+ flux in the target cells. The intracellular free Ca2+ increases on the activation of phospholipase C and formation of inositol 1, 4, 5-trisphosphate in the endothelial cells. The intracellular increase of Ca2+ activates endothelial nitric oxide synthase which leads to vascular relaxation5.

Function
AM is the most potent endogenous vasodilatory peptide found in the body6. They increase the tolerance of cells to oxidative stress, hypoxic injury and angiogenesis. It plays an important role in neurotransmission and ovarian function and in kidney, it acts as a diuretic and natriuretic7. AM is considered to play an important endocrine role in various tissues in maintaining electrolyte and fluid homeostasis8. It is used in the diagnosis and treatment of preeclampsia, type II diabetic patients and to promote fetal growth. They also play an important role in the regulation of insulin secretion and blood glucose metabolism.

References

1.     Kitamura K, Kangawa K, Kawamoto M, Ichiki Y, Nakamura S, Matsuo H, Eto T (1993). Adrenomedullin: a novel hypotensive peptide isolated from human pheochromocytoma. Biochem Biophys Res Commun., 192 (2):553-560.

2.     Ogoshi M, Nobata S, and Takei Y (2008). Potent osmoregulatory actions of homologous adrenomedullins administered peripherally and centrally in eels. Am J Physiol Regul Integr Comp Physiol, 295: 2075-2083.

3.     Ogoshi M, Inoue K, Naruse K, Takei Y (2006). Evolutionary history of the calcitonin gene-related peptide family in vertebrates revealed by comparative genomic analyses. Peptides, 27 (12):3154-3164.

4.     Cockcroft JR, Noon JP, Gardner-Medwin J, Bennett T (1997). Haemodynamic effects of adrenomedullin in human resistance and capacitance vessels. Br J Clin Pharmacol, 44(1):57-60.

5.     Shimekake Y, Nagata K, Ohta S, Kambayashi Y, Teraoka H, Kitamura K, Eto T, Kangawa K, Matsuo H (1995). Adrenomedullin stimulates two signal transduction pathways, cAMP accumulation and Ca2+ mobilization, in bovine aortic endothelial cells. J Biol Chem, 270: 4412-4417.

6.     Yanagawa B, Nagaya N (2007). Adrenomedullin: molecular mechanisms and its role in cardiac disease. Amino Acids, 32 (1):157-164.

7.     Vesely DL (2003). Natriuretic peptides and acute renal failure. Am J Physiol Renal Physiol, 285 (2):167-177.

8.     Ruzicska E, Toth M, Tulassay Z, Somogyi A (2001). Adrenomedullin and diabetes mellitus. Diabetes Metab Res Rev, 17 (5):321-329.

多肽H2N-Ser-Leu-Pro-Glu-Ala-Gly-Pro-Gly-Arg-Thr-Leu-Val-Ser-Ser-Lys-Pro-Gln-Ala-His-Gly-Ala-Pro-Ala-Pro-Pro-Ser-Gly-Ser-Ala-Pro-His-Phe-Leu-COOH的合成步骤：

1、合成CTC树脂：称取2.81g CTC Resin（如初始取代度约为0.42mmol/g）和1.42mmol Fmoc-Leu-OH于反应器中，加入适量DCM溶解氨基酸（需要注意，此时CTC树脂体积会增大好几倍，避免DCM溶液过少），再加入3.54mmol DIPEA（Mw：129.1,d：0.740g/ml），反应2-3小时后，可不抽滤溶液，直接加入1ml的HPLC级甲醇，封端半小时。依次用DMF洗涤2次，甲醇洗涤1次，DCM洗涤一次，甲醇洗涤一次，DCM洗涤一次，DMF洗涤2次（这里使用甲醇和DCM交替洗涤，是为了更好地去除其他溶质，有利于后续反应）。得到  Fmoc-Leu-CTC Resin。结构图如下：

2、脱Fmoc：加3倍树脂体积的20%Pip/DMF溶液，鼓氮气30分钟，然后2倍树脂体积的DMF 洗涤5次。得到 H2N-Leu-CTC Resin 。（此步骤脱除Fmoc基团，茚三酮检测为蓝色，Pip为哌啶）。结构图如下：

3、缩合：取3.54mmol Fmoc-Phe-OH 氨基酸，加入到上述树脂里，加适当DMF溶解氨基酸，再依次加入7.08mmol DIPEA，3.36mmol HBTU。反应30分钟后，取小样洗涤，茚三酮检测为无色。用2倍树脂体积的DMF 洗涤3次树脂。（洗涤树脂，去掉残留溶剂，为下一步反应做准备）。得到Fmoc-Phe-Leu-CTC Resin。氨基酸：DIPEA：HBTU：树脂=3：6：2.85：1（摩尔比）。结构图如下：

4、依次循环步骤二、步骤三，依次得到

H2N-Phe-Leu-CTC Resin

Fmoc-His(Trt)-Phe-Leu-CTC Resin

H2N-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Thr(tBu)-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Thr(tBu)-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Arg(Pbf)-Thr(tBu)-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Arg(Pbf)-Thr(tBu)-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Gly-Arg(Pbf)-Thr(tBu)-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Gly-Arg(Pbf)-Thr(tBu)-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Pro-Gly-Arg(Pbf)-Thr(tBu)-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Pro-Gly-Arg(Pbf)-Thr(tBu)-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Gly-Pro-Gly-Arg(Pbf)-Thr(tBu)-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Gly-Pro-Gly-Arg(Pbf)-Thr(tBu)-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Ala-Gly-Pro-Gly-Arg(Pbf)-Thr(tBu)-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Ala-Gly-Pro-Gly-Arg(Pbf)-Thr(tBu)-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Glu(OtBu)-Ala-Gly-Pro-Gly-Arg(Pbf)-Thr(tBu)-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Glu(OtBu)-Ala-Gly-Pro-Gly-Arg(Pbf)-Thr(tBu)-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Pro-Glu(OtBu)-Ala-Gly-Pro-Gly-Arg(Pbf)-Thr(tBu)-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Pro-Glu(OtBu)-Ala-Gly-Pro-Gly-Arg(Pbf)-Thr(tBu)-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Leu-Pro-Glu(OtBu)-Ala-Gly-Pro-Gly-Arg(Pbf)-Thr(tBu)-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

H2N-Leu-Pro-Glu(OtBu)-Ala-Gly-Pro-Gly-Arg(Pbf)-Thr(tBu)-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

Fmoc-Ser(tBu)-Leu-Pro-Glu(OtBu)-Ala-Gly-Pro-Gly-Arg(Pbf)-Thr(tBu)-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin

以上中间结构，均可在专肽生物多肽计算器-多肽结构计算器中，一键画出。

最后再经过步骤二得到 H2N-Ser(tBu)-Leu-Pro-Glu(OtBu)-Ala-Gly-Pro-Gly-Arg(Pbf)-Thr(tBu)-Leu-Val-Ser(tBu)-Ser(tBu)-Lys(Boc)-Pro-Gln(Trt)-Ala-His(Trt)-Gly-Ala-Pro-Ala-Pro-Pro-Ser(tBu)-Gly-Ser(tBu)-Ala-Pro-His(Trt)-Phe-Leu-CTC Resin，结构如下：

5、切割：6倍树脂体积的切割液（或每1g树脂加8ml左右的切割液），摇床摇晃 2小时，过滤掉树脂，用冰无水乙醚沉淀滤液，并用冰无水乙醚洗涤沉淀物3次，最后将沉淀物放真空干燥釜中，常温干燥24小试，得到粗品H2N-Ser-Leu-Pro-Glu-Ala-Gly-Pro-Gly-Arg-Thr-Leu-Val-Ser-Ser-Lys-Pro-Gln-Ala-His-Gly-Ala-Pro-Ala-Pro-Pro-Ser-Gly-Ser-Ala-Pro-His-Phe-Leu-COOH。结构图见产品结构图。

切割液选择：1）TFA：H2O=95%：5%

2）TFA：H2O：TIS=95%：2.5%：2.5%

3）三氟乙酸：茴香硫醚：1，2-乙二硫醇：苯酚：水=87.5%：5%：2.5%：2.5%：2.5%

（前两种适合没有容易氧化的氨基酸，例如Trp、Cys、Met。第三种适合几乎所有的序列。）

6、纯化冻干：使用液相色谱纯化，收集目标峰液体，进行冻干，获得蓬松的粉末状固体多肽。不过这时要取小样复测下纯度 是否目标纯度。

7、最后总结：

杭州专肽生物技术有限公司（ALLPEPTIDE https://www.allpeptide.com）主营定制多肽合成业务，提供各类长肽，短肽，环肽，提供各类修饰肽，如：荧光标记修饰（CY3、CY5、CY5.5、CY7、FAM、FITC、Rhodamine B、TAMRA等），功能基团修饰肽（叠氮、炔基、DBCO、DOTA、NOTA等），同位素标记肽（N15、C13），订书肽（Stapled Peptide）,脂肪酸修饰肽（Pal、Myr、Ste），磷酸化修饰肽（P-Ser、P-Thr、P-Tyr），环肽（酰胺键环肽、一对或者多对二硫键环），生物素标记肽，PEG修饰肽，甲基化修饰肽等。

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