4.6 Article

Detection of Highly Curved Membrane Surfaces Using a Cyclic Peptide Derived from Synaptotagmin-I

期刊

ACS CHEMICAL BIOLOGY
卷 7, 期 10, 页码 1629-1635

出版社

AMER CHEMICAL SOC
DOI: 10.1021/cb3002705

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资金

  1. Howard Hughes Medical Institute (HHMI) Collaborative Innovation Award
  2. National Institute of Health [MH061876]
  3. National Science Foundation [NSF IOS 1022451]
  4. Ruth L. Kirschstein National Research Service Award [F31 CA165349]
  5. NIH training grant [T32 GM008759]
  6. Direct For Biological Sciences
  7. Division Of Integrative Organismal Systems [1022451] Funding Source: National Science Foundation

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The generation of highly curved membranes is essential to cell growth, division, and movement. Recent research in the field is focused to answer questions related to the consequences of changes in the topology of the membrane once it is created, broadly termed as membrane curvature sensing. Most probes that are used to study curvature sensing are intact membrane active proteins such as DP1/Yop1p, ArfGAP1, BAR domains, and Synaptotagmin-I (Syt1). Taking a cue from nature, we created the cyclic peptide C2BL3C based on the membrane penetration C2B loop 3 of Syt1 via Click chemistry. Using a combination of spectroscopic techniques, we investigated the peptide-lipid interactions of this peptide with synthetic phospholipid vesicles and exosomes from rat blood plasma. We found that the macrocycle peptide probe was selective for lipid vesicles with highly curved surfaces (d < 100 nm). These results suggested that C2BL3C functions as a selective detector of highly curved phospholipid bilayers.

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