Jungwook Kim

Prof. Jungwook Kim


Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2019 in Carbohydrate Polymers
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Journal Article
Closed access
JAJuhong Ahn
Juhong Ahn
JRJungju Ryu
Jungju Ryu
GSGwangho Song
Gwangho Song
MWMinji Whang
Minji Whang
JKJungwook Kim
Jungwook Kim

4 January 2021 in Nature Materials
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Journal Article
Closed access
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JOJongwon Oh
Jongwon Oh
DBDahye Baek
Dahye Baek
TLTae Kyung Lee
Tae Kyung Lee
DKDongwon Kang
Dongwon Kang
HHHyeri Hwang
Hyeri Hwang
JLJiseok Lee
Jiseok Lee

1 February 2020 in Chemical Engineering Journal
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Journal Article
Closed access
CYCheolsang Yoon
Cheolsang Yoon
KYKab Pil Yang
Kab Pil Yang
JKJungwook Kim
Jungwook Kim
KSKyusoon Shin
Kyusoon Shin
KLKangtaek Lee
Kangtaek Lee

11 March 2021 in Scientific Reports
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Journal Article
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GCGyuhyeok Cho
Gyuhyeok Cho
ELEunju Lee
Eunju Lee
JKJungwook Kim
Jungwook Kim
Phosphatidylethanolamine (PE), a major component of the cellular membrane across all domains of life, is synthesized exclusively by membrane-anchored phosphatidylserine decarboxylase (PSD) in most bacteria. The enzyme undergoes auto-cleavage for activation and utilizes the pyruvoyl moiety to form a Schiff base intermediate with PS to facilitate decarboxylation. However, the structural basis for self-maturation, PS binding, and decarboxylation processes directed by PSD remain unclear. Here, we present X-ray crystal structures of PSD from Escherichia coli, representing an apo form and a PE-bound complex, in which the phospholipid is chemically conjugated to the essential pyruvoyl residue, mimicking the Schiff base intermediate. The high-resolution structures of PE-complexed PSD clearly illustrate extensive hydrophobic interactions with the fatty acyl chains of the phospholipid, providing insights into the broad specificity of the enzyme over a wide range of cellular PS. Furthermore, these structures strongly advocate the unique topology of the enzyme in a lipid bilayer environment, where the enzyme associates with cell membranes in a monotopic fashion via the N-terminal domain composed of three amphipathic helices. Lastly, mutagenesis analyses reveal that E. coli PSD primarily employs D90/D142–H144–S254 to achieve auto-cleavage for the proenzyme maturation, where D90 and D142 act in complementary to each other.

7 September 2022 in ACS Nano
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Journal Article
Closed access
DKDongwon Kang
Dongwon Kang
JLJong Ik Lee
Jong Ik Lee
BMBohee Maeng
Bohee Maeng
SLSeyeon Lee
Seyeon Lee
YKYongseok Kwon
Yongseok Kwon
JKJungwook Kim
Jungwook Kim

12 September 2024 in Nature Communications
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Journal Article
Open access
PDF file
CSChangil Son
Changil Son
JKJinyoung Kim
Jinyoung Kim
DKDongwon Kang
Dongwon Kang
SPSeojoung Park
Seojoung Park
CRChaeyeong Ryu
Chaeyeong Ryu
JLJiseok Lee
Jiseok Lee
Decoupling dynamic touch signals in the optical tactile sensors is highly desired for behavioral tactile applications yet challenging because typical optical sensors mostly measure only static normal force and use imprecise multi-image averaging for dynamic force sensing. Here, we report a highly sensitive upconversion nanocrystals-based behavioral biometric optical tactile sensor that instantaneously and quantitatively decomposes dynamic touch signals into individual components of vertical normal and lateral shear force from a single image in real-time. By mimicking the sensory architecture of human skin, the unique luminescence signal obtained is axisymmetric for static normal forces and non-axisymmetric for dynamic shear forces. Our sensor demonstrates high spatio-temporal screening of small objects and recognizes fingerprints for authentication with high spatial-temporal resolution. Using a dynamic force discrimination machine learning framework, we realized a Braille-to-Speech translation system and a next-generation dynamic biometric recognition system for handwriting.