[L010]Literature Bibliographic Information

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https://connect.patsnap.com/literature/bibliography
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Receive literature bibliography data by paper_id or doi.

One of the two parameters, paper_id and doi, is required; if both are passed, paper_id is preferred.The API supports batch requests with a maximum of 100 patents, and more patent id or patent number are separated with English comma. Batch requests are deducted from traffic/costs, and will be deducted multiple times based on the number of successful results returned.

Request Parameters

List of parameters supported by this API endpoint

NameTypeExampleDescription
doi
string10.1016/j.bpj.2024.07.030
DOI (only a single doi issupported)
paper_id
string00001b6d-2cfa-411a-ab41-8a05fd675d46,00001756-243f-4738-a288-282987105915
paper id

Response Schema

Structure of the API response data

Field NameTypeExampleDescription
data
array-
response data
doi
string10.1016/j.bpj.2024.07.030
DOI
type
stringJournal
Type
issue
string18
Issue
title
arrayPlease check the form: LiteratureTitle
Title
lang
stringEN
Language
text
stringAssessing the mechanism of facilitated proton transport across GUVs trapped in a microfluidic device
Text
author
array[ "Ruppelt, Dominik", "Ackermann, Elena L M", "Robinson, Tom", "Steinem, Claudia" ]
Author
volume
string123
Volume
abstract
arrayPlease check the form: LiteratureAbstract
Abstract
lang
stringEN
Language
text
stringProton transport across lipid membranes is one of the most fundamental reactions that make up living organisms. In vitro, however, the study of proton transport reactions can be very challenging due to limitations imposed by proton concentrations, compartment size, and unstirred layers as well as buffer exchange and buffer capacity. In this study, we have developed a proton permeation assay based on the microfluidic trapping of giant vesicles enclosing the pH-sensitive dye pyranine to address some of these challenges. Time-resolved fluorescence imaging upon a rapid pH shift enabled us to investigate the facilitated H<sup>+</sup> permeation mediated by either a channel or a carrier. Specifically, we compared the proton transport rates as a function of different proton gradients of the channel gramicidin D and the proton carrier carbonyl cyanide-m-chlorophenyl hydrazone. Our results demonstrate the efficacy of the assay in monitoring proton transport reactions and distinguishing between a channel-like and a carrier-like mechanism. This groundbreaking result enabled us to elucidate the enigmatic mode of the proton permeation mechanism of the recently discovered natural fibupeptide lugdunin.
Text
paper_id
string00001b6d-2cfa-411a-ab41-8a05fd675d46
Paper ID
pagination
string3267-3274
Pagination
publication
stringBiophysical Journal
Publication
publication_date
integer<int32>20240901
Publication Date
publication_year
string2024
Publication Year
publish_institution
stringElsevier BV
Publish Institution
status
Required
booleanfalse
Status
error_msg
stringThe request parameter format is incorrect!
Error Message
error_code
Required
integer0
Error Code

Success Response Example

Example of a successful API response

JSON
{
  "data": [
    {
      "doi": "10.1016/j.bpj.2024.07.030",
      "type": "Journal",
      "issue": 18,
      "title": [
        {
          "lang": "EN",
          "text": "Assessing the mechanism of facilitated proton transport across GUVs trapped in a microfluidic device"
        }
      ],
      "author": [
        "Ruppelt, Dominik",
        "Ackermann, Elena L M",
        "Robinson, Tom",
        "Steinem, Claudia"
      ],
      "volume": 123,
      "abstract": [
        {
          "lang": "EN",
          "text": "Proton transport across lipid membranes is one of the most fundamental reactions that make up living organisms. In vitro, however, the study of proton transport reactions can be very challenging due to limitations imposed by proton concentrations, compartment size, and unstirred layers as well as buffer exchange and buffer capacity. In this study, we have developed a proton permeation assay based on the microfluidic trapping of giant vesicles enclosing the pH-sensitive dye pyranine to address some of these challenges. Time-resolved fluorescence imaging upon a rapid pH shift enabled us to investigate the facilitated H<sup>+</sup> permeation mediated by either a channel or a carrier. Specifically, we compared the proton transport rates as a function of different proton gradients of the channel gramicidin D and the proton carrier carbonyl cyanide-m-chlorophenyl hydrazone. Our results demonstrate the efficacy of the assay in monitoring proton transport reactions and distinguishing between a channel-like and a carrier-like mechanism. This groundbreaking result enabled us to elucidate the enigmatic mode of the proton permeation mechanism of the recently discovered natural fibupeptide lugdunin."
        }
      ],
      "paper_id": "00001b6d-2cfa-411a-ab41-8a05fd675d46",
      "pagination": "3267-3274",
      "publication": "Biophysical Journal",
      "publication_date": 20240901,
      "publication_year": 2024,
      "publish_institution": "Elsevier BV"
    }
  ],
  "status": true,
  "error_code": 0
}

Error Codes

List of possible error codes returned by this endpoint

Business Errors

Error CodeDescription
68300004Invalid parameter!
68300005Search api failure!
68300006Analytic basic access error!
68300007Bad request!
68300008Service error, please try again later!
68300010The file does not comply with upload specifications!

Platform Errors

Error CodeDescription
67200000API call exceeds the total limit set by the platform!
67200001API call exceeds the total limit set by the platform!
67200002The current call rate is too fast, exceeding the current configuration limit QPS!
67200003The key and secret parameters for applying for the token are incorrect or the client has been disabled!
67200004The requested api does not have permission. Please contact our support personnel!
67200005Insufficient account balance/number of calls!
67200006The client has exceeded the activation validity period!
67200007The current call exceeds the configured usage limit of the day!
67200008Please check if the required apikey in the query parameter has been transmitted!
67200009The apikey does not match the passed bearerToken. Please check if a valid token is being used!
67200012The request is illegal!
67200100The current server status is busy, request response timeout!
67200101The API requested currently does not exist. Please check the request path!

HTTP Status Codes

Status CodeDescription
0Success
201Created
401Unauthorized
403Forbidden
404Not Found

Performance Metrics

Expected performance characteristics for this endpoint

Normal Response Time

5000 ms

Max Response Time

10000 ms