Systematic size study of an insect antifreeze protein and its interaction with ice.

Abstract:

:Because of their remarkable ability to depress the freezing point of aqueous solutions, antifreeze proteins (AFPs) play a critical role in helping many organisms survive subzero temperatures. The beta-helical insect AFP structures solved to date, consisting of multiple repeating circular loops or coils, are perhaps the most regular protein structures discovered thus far. Taking an exceptional advantage of the unusually high structural regularity of insect AFPs, we have employed both semiempirical and quantum mechanics computational approaches to systematically investigate the relationship between the number of AFP coils and the AFP-ice interaction energy, an indicator of antifreeze activity. We generated a series of AFP models with varying numbers of 12-residue coils (sequence TCTxSxxCxxAx) and calculated their interaction energies with ice. Using several independent computational methods, we found that the AFP-ice interaction energy increased as the number of coils increased, until an upper bound was reached. The increase of interaction energy was significant for each of the first five coils, and there was a clear synergism that gradually diminished and even decreased with further increase of the number of coils. Our results are in excellent agreement with the recently reported experimental observations.

journal_name

Biophys J

journal_title

Biophysical journal

authors

Liu K,Jia Z,Chen G,Tung C,Liu R

doi

10.1529/biophysj.104.051169

subject

Has Abstract

pub_date

2005-02-01 00:00:00

pages

953-8

issue

2

eissn

0006-3495

issn

1542-0086

pii

S0006-3495(05)73167-2

journal_volume

88

pub_type

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